A New Cationic Domino Process to (±)-Uleine
An amazing sequence of reactions is triggered when 1 is treated with formic acid. The formation of a benzyl cation sets off a domino reaction that ends with (±)‐uleine (2), which thus allows a simple and stereoselective synthesis of this and possibly also other natural products from the group of str...
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Veröffentlicht in: | Angewandte Chemie International Edition 1997-08, Vol.36 (13-14), p.1474-1476 |
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container_title | Angewandte Chemie International Edition |
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creator | Schmitt, Monika H. Blechert, Siegfried |
description | An amazing sequence of reactions is triggered when 1 is treated with formic acid. The formation of a benzyl cation sets off a domino reaction that ends with (±)‐uleine (2), which thus allows a simple and stereoselective synthesis of this and possibly also other natural products from the group of strychnos alkaloids. |
doi_str_mv | 10.1002/anie.199714741 |
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The formation of a benzyl cation sets off a domino reaction that ends with (±)‐uleine (2), which thus allows a simple and stereoselective synthesis of this and possibly also other natural products from the group of strychnos alkaloids.</description><identifier>ISSN: 0570-0833</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.199714741</identifier><language>eng</language><publisher>Zug: Hüthig & Wepf Verlag</publisher><subject>carbazoles ; cations ; domino reactions ; total synthesis ; uleine</subject><ispartof>Angewandte Chemie International Edition, 1997-08, Vol.36 (13-14), p.1474-1476</ispartof><rights>Copyright © 1997 by VCH Verlagsgesellschaft mbH, Germany</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3251-c49a6b8c83c96d7d87cad41db706fac4c2c286eba44815e5fdb4d0da6d4ce5e93</citedby><cites>FETCH-LOGICAL-c3251-c49a6b8c83c96d7d87cad41db706fac4c2c286eba44815e5fdb4d0da6d4ce5e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.199714741$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.199714741$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids></links><search><creatorcontrib>Schmitt, Monika H.</creatorcontrib><creatorcontrib>Blechert, Siegfried</creatorcontrib><title>A New Cationic Domino Process to (±)-Uleine</title><title>Angewandte Chemie International Edition</title><addtitle>Angew. 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Chem. Int. Ed. Engl</addtitle><date>1997-08-04</date><risdate>1997</risdate><volume>36</volume><issue>13-14</issue><spage>1474</spage><epage>1476</epage><pages>1474-1476</pages><issn>0570-0833</issn><eissn>1521-3773</eissn><abstract>An amazing sequence of reactions is triggered when 1 is treated with formic acid. The formation of a benzyl cation sets off a domino reaction that ends with (±)‐uleine (2), which thus allows a simple and stereoselective synthesis of this and possibly also other natural products from the group of strychnos alkaloids.</abstract><cop>Zug</cop><pub>Hüthig & Wepf Verlag</pub><doi>10.1002/anie.199714741</doi><tpages>3</tpages></addata></record> |
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language | eng |
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source | Wiley Online Library All Journals |
subjects | carbazoles cations domino reactions total synthesis uleine |
title | A New Cationic Domino Process to (±)-Uleine |
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