DSpace at EWHA: Total synthesis of thioamycolamide A using diastereoselective sulfa-Michael addition as the key step

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DC Field	Value	Language
dc.contributor.author	최선	*
dc.contributor.author	Pratanphorn Nakliang	*
dc.date.accessioned	2022-08-02T16:30:48Z	-
dc.date.available	2022-08-02T16:30:48Z	-
dc.date.issued	2022	*
dc.identifier.issn	2052-4129	*
dc.identifier.other	OAK-31797	*
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/261672	-
dc.description.abstract	The stereocontrolled total synthesis of the antitumor natural product thioamycolamide A has been accomplished in 14 longest linear steps and an overall yield of 19.1%. The central feature of our convergent route to this family of novel macrocyclic natural products is the preparation of the beta-alkylthio amide subunit through an auxiliary-controlled, diastereoselective sulfa-Michael addition.	*
dc.language	English	*
dc.publisher	ROYAL SOC CHEMISTRY	*
dc.title	Total synthesis of thioamycolamide A using diastereoselective sulfa-Michael addition as the key step	*
dc.type	Article	*
dc.relation.issue	15	*
dc.relation.volume	9	*
dc.relation.index	SCIE	*
dc.relation.index	SCOPUS	*
dc.relation.startpage	3998	*
dc.relation.lastpage	4002	*
dc.relation.journaltitle	ORGANIC CHEMISTRY FRONTIERS	*
dc.identifier.doi	10.1039/d2qo00747a	*
dc.identifier.wosid	WOS:000813556400001	*
dc.identifier.scopusid	2-s2.0-85133124150	*
dc.author.google	Xiao, Yi	*
dc.author.google	Jiang, Yangyang	*
dc.author.google	Xu, Chao	*
dc.author.google	Nakliang, Pratanphorn	*
dc.author.google	Yoon, Sanghee	*
dc.author.google	Choi, Sun	*
dc.author.google	Guo, Yian	*
dc.author.google	Ye, Tao	*
dc.contributor.scopusid	최선(8659831000)	*
dc.contributor.scopusid	Pratanphorn Nakliang(57216583416)	*
dc.date.modifydate	20240305081003	*