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pubmed-article:18956869pubmed:abstractTextErgot alkaloids and their synthetic analogs have been reported to exhibit broad biological activity. We investigated direct construction of the C/D ring system of ergot alkaloids based on palladium-catalyzed domino cyclization of amino allenes. With this biscyclization as the key step, total synthesis of (+/-)-lysergic acid, (+/-)-lysergol, and (+/-)-isolysergol was achieved.lld:pubmed
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pubmed-article:18956869pubmed:authorpubmed-author:OhnoHiroakiHlld:pubmed
pubmed-article:18956869pubmed:authorpubmed-author:OishiShinyaSlld:pubmed
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pubmed-article:18956869pubmed:pagination5239-42lld:pubmed
pubmed-article:18956869pubmed:dateRevised2011-5-25lld:pubmed
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pubmed-article:18956869pubmed:articleTitleTotal synthesis of (+/-)-lysergic acid, lysergol, and isolysergol by palladium-catalyzed domino cyclization of amino allenes bearing a bromoindolyl group.lld:pubmed
pubmed-article:18956869pubmed:affiliationGraduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.lld:pubmed
pubmed-article:18956869pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18956869pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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