Chemoselective N-deacetylation under mild conditions

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DC Field	Value	Language
dc.contributor.author	SULTANE, PRAKASH R.	en_US
dc.contributor.author	Trimbak B. Mete	en_US
dc.contributor.author	BHAT, RAMAKRISHNA G.	en_US
dc.date.accessioned	2019-02-25T09:00:43Z
dc.date.available	2019-02-25T09:00:43Z
dc.date.issued	2013-10	en_US
dc.identifier.citation	Organic and Biomolecular Chemistry, 12(2), 261-264.	en_US
dc.identifier.issn	1477-0520	en_US
dc.identifier.issn	1477-0539	en_US
dc.identifier.uri	http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1921	-
dc.identifier.uri	https://doi.org/10.1039/C3OB41971A	en_US
dc.description.abstract	A mild and efficient chemoselective N-deacetylation using the Schwartz reagent at room temperature in rapid time is described. The mild and neutral conditions enable orthogonal N-deacetylation in the presence of some of the common protecting groups (viz. Boc, Fmoc, Cbz, Ts). The deprotection conditions did not induce any epimerization at the chiral amino centre.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Chemoselective	en_US
dc.subject	N-deacetylation	en_US
dc.subject	Mild conditions	en_US
dc.subject	Deprotection conditions	en_US
dc.subject	Epimerization at the chiral amino centre	en_US
dc.subject	2013	en_US
dc.title	Chemoselective N-deacetylation under mild conditions	en_US
dc.type	Article	en_US
dc.contributor.department	Dept. of Chemistry	en_US
dc.identifier.sourcetitle	Organic and Biomolecular Chemistry	en_US
dc.publication.originofpublisher	Foreign	en_US
Appears in Collections:	JOURNAL ARTICLES

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