Studies on a novel safety-catch linker cleaved by Pummerer rearrangement

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/34475

Title:	Studies on a novel safety-catch linker cleaved by Pummerer rearrangement
Authors:	Tai,CH;Wu,HC;Li,WR
Contributors:	化學研究所
Keywords:	SOLID-PHASE SYNTHESIS;COMBINATORIAL LIBRARY SYNTHESIS;COMPREHENSIVE SURVEY;ORGANIC-SYNTHESIS;PEPTIDE-SYNTHESIS;STEREOSELECTIVE-SYNTHESIS;ACID;CYCLIZATION;STRATEGIES;ACTIVATION
Date:	2004
Issue Date:	2010-07-07 12:05:33 (UTC+8)
Publisher:	中央大學
Abstract:	We describe the use of a sulfide linkage as a safety-catch linker. This linker is significantly stable to acidic as well as basic conditions and allows transformations to be carried out on solid supports. Moreover, its cleavage is facile by applying Pumme
Relation:	ORGANIC LETTERS
Appears in Collections:	[Graduate Institute of Chemistry] journal & Dissertation

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