Reduction of 1-pyrrolyl and 1-indolyl carbamates to hemiaminals

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/28333

Title:	Reduction of 1-pyrrolyl and 1-indolyl carbamates to hemiaminals
Authors:	Hsu,HC;Hou,DR
Contributors:	中央大學
Keywords:	NUCLEAR-MAGNETIC-RESONANCE;DERIVATIVES;PYRROLE;INDOLE;ALKALOIDS;ANALOGS
Date:	2009
Issue Date:	2010-06-29 19:46:19 (UTC+8)
Publisher:	化學研究所
Abstract:	Hemiaminals of pyrroles and indoles have been prepared from the lithium aluminum hydride reduction of 1-pyrrolyl and 1-indolyl carbamates with good yields (67-82%). These carbamates are more reactive than aliphatic amides and carbamates under the LAH reduction, but less reactive than esters. (c) 2009 Elsevier Ltd. All rights reserved.
Relation:	TETRAHEDRON LETTERS
Appears in Collections:	[Graduate Institute of Chemistry] journal & Dissertation

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