Desymmetrization of 2,4,5,6-Tetra-O-benzyl-D-myo-inositol for the Synthesis of Mycothiol

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DC Field	Value	Language
dc.contributor.author	Chung, Chuan-Chung	en_US
dc.contributor.author	Zulueta, Medel Manuel L.	en_US
dc.contributor.author	Padiyar, Laxmansingh T.	en_US
dc.contributor.author	Hung, Shang-Cheng	en_US
dc.date.accessioned	2014-12-08T15:20:42Z	-
dc.date.available	2014-12-08T15:20:42Z	-
dc.date.issued	2011-10-21	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/ol202218n	en_US
dc.identifier.uri	http://hdl.handle.net/11536/14727	-
dc.description.abstract	An efficient chemical synthesis of mycothiol Involving the regioselective ketopinyl desymmetrization of 2,4,5,6-tetrabenzylated D-myo-inositol as the key step Is described. Together with a highly alpha-stereoselective D-glucosaminylation, the whole procedure was accomplished in eight steps with an overall yield of 40%.	en_US
dc.language.iso	en_US	en_US
dc.title	Desymmetrization of 2,4,5,6-Tetra-O-benzyl-D-myo-inositol for the Synthesis of Mycothiol	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/ol202218n	en_US
dc.identifier.journal	ORGANIC LETTERS	en_US
dc.citation.volume	13	en_US
dc.citation.issue	20	en_US
dc.citation.spage	5496	en_US
dc.citation.epage	5499	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000295817100022	-
dc.citation.woscount	5	-
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