Joined use of oxazolidinone and desymmetric amino protection: a new strategy for protection of glucosamine

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DC Field	Value	Language
dc.contributor.author	Lin, Shih-Che	en_US
dc.contributor.author	Chao, Chin-Sheng	en_US
dc.contributor.author	Chang, Chiu-Ching	en_US
dc.contributor.author	Mong, Kwok-Kong T.	en_US
dc.date.accessioned	2014-12-08T15:07:03Z	-
dc.date.available	2014-12-08T15:07:03Z	-
dc.date.issued	2010-04-07	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2010.02.021	en_US
dc.identifier.uri	http://hdl.handle.net/11536/5522	-
dc.description.abstract	Joined use of N-benzyl oxazolidinone and N-benzyl-N-benzyloxycarbonyl (N-BnCbz) desymmetric amino-protecting function is reported. The new synthetic approach enables the facile preparation of type I and type 2 LacNAc disaccharides in satisfactory yields. One-pot deprotection of N-BnCbz and O-benzyl ether is achieved by hydrogenolysis under mild conditions. (C) 2010 Elsevier Ltd. All rights reserved.	en_US
dc.language.iso	en_US	en_US
dc.title	Joined use of oxazolidinone and desymmetric amino protection: a new strategy for protection of glucosamine	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/j.tetlet.2010.02.021	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	51	en_US
dc.citation.issue	14	en_US
dc.citation.spage	1910	en_US
dc.citation.epage	1913	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:000275920600026	-
dc.citation.woscount	4	-
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