IBS Publications Repository: Biomimetic total synthesis of (±)-berkeleyamide D

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Biomimetic total synthesis of (±)-berkeleyamide D

DC Field	Value	Language
dc.contributor.author	Deokhee Jo	-
dc.contributor.author	Sunkyu Han	-
dc.date.available	2017-09-05T05:22:33Z	-
dc.date.created	2017-04-24	-
dc.date.issued	2017-04	-
dc.identifier.issn	2052-4129	-
dc.identifier.uri	https://pr.ibs.re.kr/handle/8788114/3734	-
dc.description.abstract	We describe the total synthesis of (±)-berkeleyamide D using a biosynthetically inspired strategy. The spirocyclic core of berkeleyamide D was constructed via sequential epoxidations and a late-stage base-mediated cyclization of a biosynthetically relevant precursor. Our synthetic solution might be applicable to access other fungal natural products of this family. © the Partner Organisations 2017	-
dc.description.uri	1	-
dc.language	영어	-
dc.publisher	ROYAL SOC CHEMISTRY	-
dc.title	Biomimetic total synthesis of (±)-berkeleyamide D	-
dc.type	Article	-
dc.type.rims	ART	-
dc.identifier.wosid	000398911900002	-
dc.identifier.scopusid	2-s2.0-85016399783	-
dc.identifier.rimsid	59276	ko
dc.date.tcdate	2018-10-01	-
dc.contributor.affiliatedAuthor	Deokhee Jo	-
dc.contributor.affiliatedAuthor	Sunkyu Han	-
dc.identifier.doi	10.1039/c6qo00812g	-
dc.identifier.bibliographicCitation	ORGANIC CHEMISTRY FRONTIERS, v.4, no.4, pp.506 - 509	-
dc.citation.title	ORGANIC CHEMISTRY FRONTIERS	-
dc.citation.volume	4	-
dc.citation.number	4	-
dc.citation.startPage	506	-
dc.citation.endPage	509	-
dc.date.scptcdate	2018-10-01	-
dc.description.wostc	2	-
dc.description.scptc	2	-
dc.description.journalClass	1	-
dc.description.journalRegisteredClass	scie	-
dc.description.journalRegisteredClass	scopus	-