Organic Syntheses

<!DOCTYPE html> <html xmlns="https://www.w3.org/1999/xhtml" xml:lang="en"> <head id="ctl00_Head1">  <script async src="https://www.googletagmanager.com/gtag/js?id=G-TEDQYNWKCX"></script> <script> window.dataLayer = window.dataLayer || []; function gtag() { dataLayer.push(arguments); } gtag('js', new Date()); gtag('config', 'G-TEDQYNWKCX'); </script> <title> Organic Syntheses </title><link href="Styles/Site.css" rel="stylesheet" type="text/css" /><link rel="stylesheet" href="Styles/jquery-ui.css" /> <script type="text/javascript" src="https://code.jquery.com/jquery-1.9.1.js"></script> <script type="text/javascript" src="https://code.jquery.com/ui/1.10.2/jquery-ui.js"></script> <script src="https://cdn.jsdelivr.net/npm/sweetalert2@11"></script>  <script type="text/javascript"> $(function () { $("#tabs").tabs({ activate: function (event, ui) { var active = $("#tabs").tabs("option", "active"); if (active != null && (active.valueOf() == 1 || active.valueOf() == 0)) { $("#tabs").tabs("option", "active", active); setCookie("quickSearchTab", active.toString(), 30); } } }); var tabCookie = getCookie("quickSearchTab") if (tabCookie == null || tabCookie == "") { $("#tabs").tabs("option", "active", 0); setCookie("quickSearchTab", "0", 30); } else { if (tabCookie == "1") { $("#tabs").tabs("option", "active", 1); } else { $("#tabs").tabs("option", "active", 0); } } }); function setCookie(cname, cvalue, exdays) { var d = new Date(); d.setTime(d.getTime() + (exdays * 24 * 60 * 60 * 1000)); var expires = "expires=" + d.toGMTString(); document.cookie = cname + "=" + cvalue + "; " + expires; } function getCookie(cname) { var name = cname + "="; var ca = document.cookie.split(';'); for (var i = 0; i < ca.length; i++) { var c = ca[i].trim(); if (c.indexOf(name) == 0) return c.substring(name.length, c.length); } return ""; } function jsGoto(attr) { window.location.hash = ""; window.location.hash = attr; } function showPdf(sender) { document.getElementById("pdfFrame").src = sender; document.getElementById("pdfFrame").src = document.getElementById("pdfFrame").src; // document.getElementById("exchangablediv").setAttribute("innerHTML","<a id='pdfContainer' href='" + sender + "' class='media'></a>"); // $('a.media').media({ width: 1000, height: 2000 }); $find('ModalBehaviorId').show(); } // and to hide the modal, we are going to use $fin('behaviourIDofTheModal').hide(); function hidePdf() { document.getElementById("pdfFrame").src = ""; document.getElementById("pdfFrame").src = document.getElementById("pdfFrame").src; // document.getElementById("exchangablediv").setAttribute("innerHTML","<a id='pdfContainer' href='" + sender + "' class='media'></a>"); // $('a.media').media({ width: 1000, height: 2000 }); $find('ModalBehaviorId').hide(); } function resizing() { } function bodyOnLoad() { } function updateContentWrapper(delta) { /* if (delta == null) { delta = 0; } var a = $(window).height() - 330 - delta; b = document.getElementById("ContentWrapper"); if (a >= 300) { b.setAttribute("style", " overflow:scroll;overflow-x: hidden;height:" + a.toString() + "px"); //b.style.height = a.toString() + "px"; } else { b.css("height","300px");} */ } function updateMinContentWrapper(delta) { if (delta == null) { delta = 0; } var a = $(window).height() - 330 - delta; b = document.getElementById("ContentWrapper"); if (b != null) { if (a >= 300) { b.setAttribute("style", " overflow:scroll;overflow-x: hidden; min-height:" + a.toString() + "px"); //b.style.height = a.toString() + "px"; } else { $("#b").css("min-height", "300px"); } } } function log(message) { } function meQSfocus(a) { var meId = a.id; if (a.className == "textQuickSearchRight") { sorc = "HttpHandlers/AutoComplete.asmx/GetFullText"; } else { var meIdParent = $(a).parent().parent().parent().get(0); var z = $(meIdParent).find('select[id*="Type"]').get(0).value; var sorc = "" switch (z) { case "CAS": sorc = "HttpHandlers/AutoComplete.asmx/GetCas"; break; case "Compound Name": sorc = "HttpHandlers/AutoComplete.asmx/GetSynonym"; break; case "Title": sorc = "HttpHandlers/AutoComplete.asmx/GetTitle"; break; case "Author": sorc = "HttpHandlers/AutoComplete.asmx/GetAuthor"; break; case "Checked by": sorc = "HttpHandlers/AutoComplete.asmx/GetChecker"; break; case "Anywhere": sorc = "HttpHandlers/AutoComplete.asmx/GetFullText"; break; default: break; } } $(a).autocomplete({ source: sorc, minLength: 2, select: function (event, ui) { log(ui.item ? 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$(this).text()); totalHeight += $(this).height(); totalWidth += $(this).width(); if ($(this).width() / $(this).height() < sliderRatio) { sliderRatio = $(this).width() / $(this).height(); } }); }); $(".collapsibleContainer").collapsiblePanel(); resizing(); //getMaxTitle(); //funcMagnify(); //getMaxTitle(); elems = $(".homeArticle"); for (var i = 0; i < elems.length; i++) { $(elems[i]).css("height", "auto"); } }; </script>  <script type="text/javascript"> function bodyOnLoad() { } function resizing() { if (gWidth != Math.round(document.getElementById("ctl00_MainContent_Left").clientWidth)) { var leftWidth = document.getElementById("ctl00_MainContent_Left").clientWidth; var elems = document.getElementsByTagName('*'); //// for (var i = 0; i < elems.length; i++) { if ((' ' + elems[i].className + ' ').indexOf(' ' + 'articleBody' + ' ') > -1 || (' ' + elems[i].className + ' ').indexOf(' ' + 'articleBodySlim' + ' ') > -1) { if (leftWidth < 650) { elems[i].className = "articleBodySlim"; } else { elems[i].className = "articleBody"; } } } /// } gWidth = Math.round(document.getElementById("ctl00_MainContent_Left").clientWidth); if (leftWidth > 650) { getMaxTitle(); funcMagnify(); getMaxTitle(); } //funcMagnify(); } function toggleCollapse() { var elems = document.getElementsByTagName('*'); //// for (var i = 0; i < elems.length; i++) { if ((' ' + elems[i].className + ' ').indexOf(' ' + 'collapseImgDiv' + ' ') > -1) { $(elems[i]).css("min-height", "0px"); var c = elems[i].clientHeight; if (c > maxCheckHeight) { maxArticleBodyHeight = c; } } } /// elems = $(".homeArticle"); for (var i = 0; i < elems.length; i++) { if ($("#magnifier").slider("value") < document.getElementById("ctl00_MainContent_Left").clientWidth * 0.5 && maxArticleBodyHeight > 700) { $(elems[i]).css("height", maxArticleBodyHeight + maxTitleHeight + maxAuthorHeight + maxCheckHeight + 140); } else { $(elems[i]).css("height", "auto"); } } var divs = $(document).find('div.collapsibleContainer'); for (var i = 0; i < divs.length; i++) { $(".collapsibleContainerContent", $(divs[i]).parent()).slideToggle(); } divs = document.getElementsByName('expandtext'); for (var j = 0; j < divs.length; j++) { if (divs[j].innerHTML == "Collapse") { divs[j].innerHTML = "Expand"; divs[j].title = "Expand title reaction"; } else { divs[j].innerHTML = "Collapse"; divs[j].title = "Expand title reaction"; } } } function resizeArticle(sender) { if (sender.width < 900) { sender.setAttribute('width', '100%'); } else { sender.setAttribute('width', '450px'); } } function showKetcher() { //document.getElementById("ketcherFrame").src = document.getElementById("ketcherFrame").src; $('iframe#ketcherFrame').attr('src', 'Scripts\\standalone\\index.html'); $find('KetcherBehaviorId').hide(); $find('KetcherBehaviorId').show(); var a = setTimeout(populateKetcher, 3000); } function populateKetcher() { //alert("now"); var ktxt = document.getElementById('ctl00_MainContent_SearchStructureMol').value.toString(); if (ktxt != null && ktxt != "") { //var ketcher = getKetcher(); var ketcherFrame = document.getElementById('ketcherFrame'); var ketcher = null; if ('contentDocument' in ketcherFrame) ketcher = ketcherFrame.contentWindow.ketcher; else // IE7 ketcher = document.frames['ketcherFrame'].window.ketcher; if (ketcher == null) { ketcher = document.frames['ketcherFrame'].window.ketcher; } ketcher.setMolecule(ktxt); } } function getKetcher() { var frame = null; if ('frames' in window && 'ketcherFrame' in window.frames) frame = window.frames['ketcherFrame']; else return null; if ('window' in frame) return frame.window.ketcher; } function getMaxTitle() { maxTitleHeight = 0; maxAuthorHeight = 0; maxCheckHeight = 0; var elemtest = $(".procTitle"); for (var j = 0; j < elemtest.length; j++) { $(elemtest[j]).css("min-height", "0px"); var a = elemtest[j].clientHeight; if (a > maxTitleHeight) { maxTitleHeight = a; } } for (var j = 0; j < elemtest.length; j++) { $(elemtest[j]).css("min-height", maxTitleHeight); } elemtest = $(".homeAuthors"); for (var j = 0; j < elemtest.length; j++) { $(elemtest[j]).css("min-height", "0px"); var a = elemtest[j].clientHeight; if (a > maxAuthorHeight) { maxAuthorHeight = a; } } for (var j = 0; j < elemtest.length; j++) { $(elemtest[j]).css("min-height", maxAuthorHeight); } elemtest = $(".procCheck"); for (var j = 0; j < elemtest.length; j++) { $(elemtest[j]).css("min-height", "0px"); var a = elemtest[j].clientHeight; if (a > maxCheckHeight) { maxCheckHeight = a; } } for (var j = 0; j < elemtest.length; j++) { $(elemtest[j]).css("min-height", maxAuthorHeight); } /// // resizeTitles(); ///////////// var elems = document.getElementsByTagName('*'); //// for (var i = 0; i < elems.length; i++) { if ((' ' + elems[i].className + ' ').indexOf(' ' + 'collapseImgDiv' + ' ') > -1) { $(elems[i]).css("min-height", "0px"); var c = elems[i].clientHeight; if (c > maxCheckHeight) { maxArticleBodyHeight = c; } } } /// elems = $(".homeArticle"); for (var i = 0; i < elems.length; i++) { if ($("#magnifier").slider("value") < document.getElementById("ctl00_MainContent_Left").clientWidth * 0.5) { $(elems[i]).css("height", maxArticleBodyHeight + maxTitleHeight + maxAuthorHeight + maxCheckHeight + 140); } else { $(elems[i]).css("height", "auto"); } } ////////////// } function funcMagnify() { var wdth = 0; try { //$("#sliderContainer").height($("#sliderContainer").width()/sliderRatio); } catch (ex) { } try { wdth = $("#magnifier").slider("value") } catch (ex) { wdth = document.getElementById("ctl00_MainContent_Left").clientWidth * 0.5 } //alert(wdth); //var elems = document.getElementsByTagName('*'); //// var elems = $(".articleBody"); for (var i = 0; i < elems.length; i++) { $(elems[i]).css("width", wdth + "px"); // $(elems[i]).css("height", $("#magnifier").slider("value") + maxTitleHeight + maxAuthorHeight + maxCheckHeight + 90 + "px"); if (wdth > document.getElementById("ctl00_MainContent_Left").clientWidth * 0.5) { $(elems[i]).css("margin", "0 auto"); $(elems[i]).css("float", "none"); $(".collapseImgDiv").css("vertical-align", "auto"); } else { $(elems[i]).css("float", "left"); $(".collapseImgDiv").css("vertical-align", "middle"); } } elems = $(".homeArticle"); for (var i = 0; i < elems.length; i++) { $(elems[i]).css("width", wdth * 0.9 + "px"); } elems = $(".collapsibleContainer"); for (var i = 0; i < elems.length; i++) { $(elems[i]).css("width", wdth * 0.9 * 0.95 + "px"); // $(elems[i]).css("height", $("#magnifier").slider("value") * 0.9 * 0.95 + "px"); } elems = $(".collapseImgDiv"); for (var i = 0; i < elems.length; i++) { $(elems[i]).css("height", wdth * 0.9 * 0.95 - 70 + "px"); $(elems[i]).css("width", wdth * 0.9 * 0.95 + "px"); } elems = $(".collapsibleContainerContent"); for (var i = 0; i < elems.length; i++) { $(elems[i]).css("height", wdth * 0.9 * 0.95 - 70 + "px"); } elems = $(".collapseImgRes"); for (var i = 0; i < elems.length; i++) { if (wdth > document.getElementById("ctl00_MainContent_Left").clientWidth * 0.5) { $(elems[i]).parent().css("height", $(elems[i]).get(0).clientHeight + 10 + "px"); $(elems[i]).parent().parent().css("height", $(elems[i]).get(0).clientHeight + 10 + "px"); } } } function zoomArticle(a) { //$("#magnifier").slider("value") var b = $("#magnifier").slider("value") + a; if (b > $("#magnifier").slider("option", "max")) { b = $("#magnifier").slider("option", "max"); } if (b < $("#magnifier").slider("option", "min")) { b = $("#magnifier").slider("option", "min"); } $("#magnifier").slider("value", b); } async function ClientSaveStructure(a) { var ketcherFrame = document.getElementById('ketcherFrame'); var ketcher = null; if ('contentDocument' in ketcherFrame) ketcher = ketcherFrame.contentWindow.ketcher; else // IE7 ketcher = document.frames['ketcherFrame'].window.ketcher; //document.getElementById('ctl00_MainContent_SearchStructure').value = ketcher.getSmiles(); document.getElementById('ctl00_MainContent_SearchStructure').value = await ketcher.getMolfile(); document.getElementById('ctl00_MainContent_StructureModalPanel').setAttribute("style", "display:none;"); if (a == 1) { warnUser('ketcherSrc'); return false; } if (a == 0) { __doPostBack('RenderStructure', '') } } </script> <script type="text/javascript"> function press() { var a = document.activeElement; } </script> <style type="text/css"> .page { /* background-color: #F4F5E7 !important;*/ } #content .ui-widget-header { background-color: inherit !important; } #content .ui-widget-content { background-color: white !important; } .item img { max-height: 150px; width: auto !important; } .medialinks{font-size:14px;} .medialinks:hover{color:inherit;} .medialinks:visited{color:inherit;} </style> <style type="text/css"> .ctl00_NavigationMenu_0 { background-color:white;visibility:hidden;display:none;position:absolute;left:0px;top:0px; } .ctl00_NavigationMenu_1 { text-decoration:none; } .ctl00_NavigationMenu_2 { } .ctl00_NavigationMenu_3 { border-style:none; } .ctl00_NavigationMenu_4 { } 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Reisman, Volume Editor</a></div> </div>   <div style="width:100%"> <div width="90%" id="qwe" style="margin-top: 2px; height: 60px;"> <div class="articleBody1"> <div class="homeArticle1" style="background: none; border: 0; min-height: 50px; margin-bottom: 10px;"> <table style="float: left;"> <tr> <td> <img src="Styles/images/minus.png" style="width: 15px;" onclick="javascript:zoomArticle(-10);" /> </td> <td style="padding-right: 10px; padding-left: 10px;"> <div id="magnifier" class="magnifier"> </div> </td> <td> <img src="Styles/images/minus.png" style="width: 25px;" onclick="javascript:zoomArticle(10);" /> </td> </tr> <tr> <td colspan="3" style="vertical-align: top; text-align: center; font-size: 14px; font-weight: bold;"> Zoom Articles Display </td> </tr> </table> </div> </div> <div class="articleBody1"> <div class="homeArticle1" style="background: none; border: 0; min-height: 0px; margin-bottom: 10px;"> <div id="Toggle all" style="width: 100%; height: 50px;"> <div id="Div1" style="width: 200px; height: 40px; float: right; margin-right: 4%;" onclick="toggleCollapse();" class="RoundYellowDiv"> <div style="float: left; margin-left: 5px; margin-top: 3px;"> <img src="Styles/view_fullscreen.png" style="height:35px;"/> </div> <div style="margin-right: 50px; height: 95%; vertical-align: middle;"> <table style="height: 100%"> <tr> <td style="height: 100%; vertical-align: middle; text-align: right; color: white; font-weight: bold; font-size: 10px; font-family: Sans-Serif;"> Toggle all articles expansion </td> </tr> </table> </div> </div> </div> </div> </div> </div> </div>  <div style="width:100%" > <div id="ctl00_MainContent_ArticlePanel" style="text-align:center;"> <div id="ctl00_MainContent_Articles" style="margin-top: 10px;"><div id='content' width='100%'> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">1</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Nitrosation of Diphenylamine with 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide (NO-1) </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Pravien S. Rajaram, Keerthana Chakkanalil, and Ryan D. Baxter </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 478 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0478 </div> <div class="procCheck">Checked by: Haoran Xiong, Hirofumi Ueda, and Hidetoshi Tokuyama<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0478 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0478.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">2</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Oxygen-free alkene hydration using nitroarenes: Diastereoselective hydration of cholesteryl acetate </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Jonas Elfert, Anup Bhunia, and Armido Studer </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 460 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0460 </div> <div class="procCheck">Checked by: Ibrahim-Ethem Celik and Christopher D. Vanderwal<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0460 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0460.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">3</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> <font style="color:red;">Discussion Addendum</font> for: Palladium-catalyzed Buchwald-Hartwig Amination and Suzuki-Miyaura Cross-coupling Reaction of Aryl Mesylates </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Yu Kiu Lau, Man Ho Tse, Pui Ying Choy, and Fuk Yee Kwong </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 438 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0438 </div> <div class="procCheck"><b>Original Article: </b><a style='text-decoration:none' href='demo.aspx?prep=v93p0014'><i>Org. Synth.</i> <b>2016</b>, <i>93</i>, 14</a><br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0438 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0438.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">4</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> <font style="color:red;">Discussion Addendum</font> for: Preparation of 2-(2-(Dicyclohexylphosphino)phenyl)-1-methyl-1H-indole (CM-phos) </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Cheuk Lam Cheung, Pui Ying Choy, Man Ho Tse, and Fuk Yee Kwong </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 423 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0423 </div> <div class="procCheck"><b>Original Article: </b><a style='text-decoration:none' href='demo.aspx?prep=v92p0195'><i>Org. Synth.</i> <b>2015</b>, <i>92</i>, 195</a><br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0423 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0423.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">5</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Synthesis of 3-Azabicyclo[3.2.0]heptane hydrochloride </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Carl M. F. Mansson and Noah Z. Burns </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 410 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0410 </div> <div class="procCheck">Checked by: J. Andrew P. Maitland, Daniel J. Cox and Darren J. Dixon<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0410 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0410.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">6</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Preparation of <i>S</i>-Methyl Methanethiosulfonate from Dimethyl Sulfoxide Initiated by Oxalyl Chloride </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Xixuan Zhao, Shuai Peng, Hao Wang, Shuai Huang, Baoguo Sun, Hongyu Tian and Sen Liang </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 395 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0395 </div> <div class="procCheck">Checked by: Roberto Tinelli, Sophie Woolford and Nuno Maulide<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0395 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0395.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">7</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> α-Arylation of N-Boc Pyrrolidine </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Kevin Campos, Melissa Cummings, Hengyu Li, and Feng Peng </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 382 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0382 </div> <div class="procCheck">Checked by: Mott and Sarah E. Reisman<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0382 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0382.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">8</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Synthesis of 3,3-Dimethyl-nitroso-2,3-dihydrobenzo[<i>d</i>]isothiazole 1,1-dioxide (NO-1) </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Keerthana Chakkanalil, Pravien S. Rajaram, and Ryan D. Baxter </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 366 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0366 </div> <div class="procCheck">Checked by: Haoran Xiong, Hirofumi Ueda, and Hidetoshi Tokuyama<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0366 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="height:95%" alt="Reaction scheme" src="/content/figures/v101p0366.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">9</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Preparation of Highly Reactive Lithium Metal Dendrites and the Synthesis of (Trimethylsilyl)methyllithium </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Raquel M. Gonzalez, Han-Hsiang Hsu, and Andy A. Thomas </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 342 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0342 </div> <div class="procCheck">Checked by: Bilal Altundas and Scott E. Denmark<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0342 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0342.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">10</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Hydration of Nitriles to Primary Amides Enabled by the Ghaffar-Parkins Catalyst </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Daniel W. Turner, Allison T. Hands, and Neil K. Garg </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 327 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0327 </div> <div class="procCheck">Checked by: Kohta Ide, Juri Sakata, and Hidetoshi Tokuyama<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0327 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0327.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">11</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Synthesis of Benzyl-δ-Truxinate via Enantioselective [2+2] Photocycloaddition </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Rodrigo Villanueva, Ellie F. Plachinski, and Tehshik P. Yoon </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 309 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0309 </div> <div class="procCheck">Checked by: Yu-Che Chang and M. Kevin Brown<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0309 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0309.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">12</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> <font style="color:red;">Discussion Addendum</font> for: Palladium-Catalyzed Dehydrative Allylation of Hypophosphorous Acid with Allylic Alcohols. Preparation of Cinnamyl-H-Phosphinic Acid </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Karla Bravo-Altamirano and Jean-Luc Montchamp </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 295 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0295 </div> <div class="procCheck"><b>Original Article: </b><a style='text-decoration:none' href='demo.aspx?prep=v85p0096'><i>Org. Synth.</i> <b>2008</b>, <i>85</i>, 96</a><br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0295 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0295.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">13</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Synthesis of <i>S,S</i>-Di(pyridin-2-yl)carbonodithioate (DPDTC) for the Reduction of Carboxylic Acids </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Karthik S. Iyer, Jordan R. Yirak, Hubert Muchalski, and Bruce H. Lipshutz </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 274 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0274 </div> <div class="procCheck">Checked by: Anna A. M. Miller, Daniel Rozsar and Darren J. Dixon<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0274 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0274.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">14</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> One-pot Synthesis of Alkynes from Esters via a Tandem Reduction-Ohira-Bestmann Reaction </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Cholapat Varongchayakul and Rick L. Danheiser </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 258 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0258 </div> <div class="procCheck">Checked by: Hojoon Park and Kevin R. Campos<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0258 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0258.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">15</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Preparation of 2-Chloro-1-(1-ethoxyvinyl)pyridinium Triflate </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> John P. Frank, William R. Strutton, Joel K. A. Adade, and Max M. Majireck </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 242 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0242 </div> <div class="procCheck">Checked by: Christopher C. Nawrat and Kevin Campos <br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0242 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0242.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">16</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Platinum-Catalyzed Enantioselective Diboration of Monosubstituted Alkenes </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Chenpeng Gao, Paul S. Lee, and James P. Morken </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 229 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0229 </div> <div class="procCheck">Checked by: Matthieu Maciejewski and Tehshik Yoon<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0229 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0229.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">17</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Chromatography-Free and Chlorinated Solvent-Free Preparation of 2,5-dibromohexanediamide (DBHDA) </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Ben Bower, Sébastien R. G. Galan, and Benjamin G. Davis </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 207 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0207 </div> <div class="procCheck">Checked by: Ruby Long Ying Chan and Pauline Chiu<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0207 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="height:95%" alt="Reaction scheme" src="/content/figures/v101p0207.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">18</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Intramolecular Coupling for General Synthesis of Backbone Substituted Bicyclo[1.1.1]pentyl Boronates </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Jet Tsien, Yangyang Yang, René García-Del Valle, Jonathan M. E. Hughes, Byron K. Peters, Rohan R. Merchant, and Tian Qin </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 181 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0181 </div> <div class="procCheck">Checked by: Sota Akiyama, Paul Sinclair and Richmond Sarpong<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0181 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="height:95%" alt="Reaction scheme" src="/content/figures/v101p0181.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">19</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Difluoromethylation of Phenols </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Allison T. Hands, Zachary G. Walters, Jacob P. Sorrentino, and Neil K. Garg </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 164 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0164 </div> <div class="procCheck">Checked by: Yi Xiao, Milos Vavrik and Nuno Maulide<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0164 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0164.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">20</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Nickel-catalyzed Amination of Aryl Chlorides </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Zachary G. Walters, Daniel W. Turner, and Neil K. Garg </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 150 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0150 </div> <div class="procCheck">Checked by: Prashansa B. Kannangara and M. Kevin Brown<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0150 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0150.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">21</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Tandem Fragmentation/Olefination for Production of Neopentylene-Tethered 1,6-Enynes from Dimedone </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Kh Tanvir Ahmed, A. C. Martin, Gabriella O. Wabler, Kristen S. Nerbecki, and Gregory B. Dudley </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 124 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0124 </div> <div class="procCheck">Checked by: Hyung Joo Kim and Tehshik Yoon<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0124 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0124.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">22</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Synthesis of 5-(1-Diazo-2-ethoxy-2-oxoethyl) dibenzo[<i>b,d</i>]thiophenium Triflate </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Brigitte Worbs, Sven Timmann, Feng Peng, Ralph Zhao, and Manuel Alcarazo </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 109 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0109 </div> <div class="procCheck">Checked by: Partha Sarathi Hazra and Kevin Brown<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0109 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0109.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">23</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> <font style="color:red;">Discussion Addendum</font> for: Mild Conversion of Tertiary Amides to Aldehydes Using Cp<sub>2</sub>Zr(H)Cl (Schwartz's Reagent) </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Narsihmulu Cheryala, Rui Shi, Shelby Mcguire, Naresh Gantasala, Nagarjun Reddy Vantaddu, Ravikrishna Dada, Nan Wang, Shameem S. Syeda, Hira Khalid, and Gunda I. Georg </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 81 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0081 </div> <div class="procCheck"><b>Original Article: </b><a style='text-decoration:none' href='demo.aspx?prep=v88p0427'><i>Org. Synth.</i> <b>2011</b>, <i>88</i>, 427</a><br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0081 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0081.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">24</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Preparation of Radical Clocks Bearing Carbonyl Groups: Synthesis of <i>N-</i>Methoxy-<i>N</i>-methylspiro[cyclopropane-1,9'-fluorene]-2-carboxamide </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Nicole D. Bartolo, Ryan N. Robson, Collin H. Witt, and K. A. Woerpel </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 61 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0061 </div> <div class="procCheck">Checked by: Kevin Lee and Dirk Trauner<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0061 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0061.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">25</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Cobalt-catalyzed Radical Olefin Isomerization: Retrocycloisomerization of (-)-Caryophyllene Oxide to (-)-Humulene Oxide II </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Eleanor M. Landwehr and Ryan A. Shenvi </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 51 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0051 </div> <div class="procCheck">Checked by: Emily P. Chen and Sarah E. Reisman<br /></div> </div>  </div> <br/> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%;"> <div class="collapsibleContainer" id=v101p0051 name='1' style="width: 100%;"> <div class="collapseImgDiv"> <img class="collapseImgRes" style="width:95%" alt="Reaction scheme" src="/content/figures/v101p0051.gif" /> </div> </div> </div> </div> </div> <div class="articleBody"> <div class="homeArticle"> <div style=" color: rgb(180,180,180); float: right; position: static; top: 0px; margin-left: 3px; font-size:16px; font-weight:normal; text-shadow: 0px 1px 0px #fffeef; filter: dropshadow(color=#fffeef,offX=0,offY=1); ">26</div> <div style="display: inline-block; width: 95%; margin-left: 2%; margin-right: 2%; margin-top:0px;">  <div class="procTitle" style="width: 100%; font-size: 14px; font-weight: bold;"> Metal-Free Aziridination of Alkenes with Free Amines by Thianthrenation </div>  <div style="float: left; font-size: 12px; margin-top: 10px;"> <div class="homeAuthors"> Ming-Shang Liu and Wei Shu </div> <div> <i>Org. Synth.</i> <b>2024</b>, <i>101</i>, 34 </div> <div class="tocdoi"> DOI: 10.15227/orgsyn.101.0034 </div> <div class="procCheck">Checked by: Michael D. 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