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Novel Ring Contractions via [2,3] Wittig Type Rearrangements: Synthesis of 2-Desoxy-2-methylenebicyclomycin

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dc.contributor.authorWilliams, Robert M.-
dc.contributor.authorSabol, Mark R.-
dc.contributor.authorKim, Hee-Doo-
dc.contributor.authorKwast, Andrzej-
dc.date.accessioned2023-12-18T10:31:23Z-
dc.date.available2023-12-18T10:31:23Z-
dc.date.issued1991-08-
dc.identifier.issn0002-7863-
dc.identifier.issn1520-5126-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/159233-
dc.description.abstractBridgehead carbanion generation of bicyclo[5.2.2] and bicycio[7.2.2] allyl ether bridged piperazinediones result in novel ring contractions via unusual [2,3] Wittig type and [3,3] Claisen rearrangements. The application of the [2,3] Wittig rearrangements to the construction of 2-desoxy-2-methylenebicyclomycin (3) is described. © 1991, American Chemical Society. All rights reserved.-
dc.format.extent13-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleNovel Ring Contractions via [2,3] Wittig Type Rearrangements: Synthesis of 2-Desoxy-2-methylenebicyclomycin-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/ja00017a039-
dc.identifier.scopusid2-s2.0-0025743182-
dc.identifier.wosidA1991GB29800039-
dc.identifier.bibliographicCitationJournal of the American Chemical Society, v.113, no.17, pp 6621 - 6633-
dc.citation.titleJournal of the American Chemical Society-
dc.citation.volume113-
dc.citation.number17-
dc.citation.startPage6621-
dc.citation.endPage6633-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.urlhttps://pubs.acs.org/doi/abs/10.1021/ja00017a039-
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