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dc.contributor.author고수영-
dc.date.accessioned2016-08-27T02:08:11Z-
dc.date.available2016-08-27T02:08:11Z-
dc.date.issued2010-
dc.identifier.issn0022-3263-
dc.identifier.otherOAK-6957-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/216482-
dc.description.abstractA sythesis oseltamivir (Tamiflu) was achieved starting from D-mannitol A unique feature of the synthetic route is that an acyelic processor was constructed which was then cyclized in an ultramolecular aldol reaction to form the Tamiflu skeletion Throughout the synthesis well-established. highly efficient reactions were employed, and no protecion/deprotection sequence was needed-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleA Synthesis of Oseltamivir (Tamiflu) Starting from D-Mannitol-
dc.typeArticle-
dc.relation.issue20-
dc.relation.volume75-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage7006-
dc.relation.lastpage7009-
dc.relation.journaltitleJOURNAL OF ORGANIC CHEMISTRY-
dc.identifier.doi10.1021/jo.101517g-
dc.identifier.wosidWOS:000282604900036-
dc.identifier.scopusid2-s2.0-79952201998-
dc.author.googleKo, Ji S.-
dc.author.googleKeum, Ji E.-
dc.author.googleKo, Soo Y.-
dc.contributor.scopusid고수영(7403325351)-
dc.date.modifydate20230208103927-
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자연과학대학 > 화학·나노과학전공 > Journal papers
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