Asymmetric synthesis of 4- and 5-substituted pipecolic esters by ring-closing metathesis and palladium-catalyzed formate reduction

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/33927

Title:	Asymmetric synthesis of 4- and 5-substituted pipecolic esters by ring-closing metathesis and palladium-catalyzed formate reduction
Authors:	Sun,Chong-Si;Lin,Yu-Shiang;Hou,Duen-Ren
Contributors:	化學研究所
Keywords:	ACID-DERIVATIVES;(2S;4R)-4-HYDROXYPIPECOLIC ACID;ENANTIOSELECTIVE SYNTHESIS;STEREOSELECTIVE-SYNTHESIS;THROMBIN INHIBITORS;POTENT;ALKYLATION;EFFICIENT
Date:	2008
Issue Date:	2010-07-07 11:53:43 (UTC+8)
Publisher:	中央大學
Abstract:	Asymmetric synthesis of 4- and 5-substituted pipecolic esters was achieved by the sequence of allylation, ring-closing metathesis, and palladium-catalyzed formate reduction.
Relation:	JOURNAL OF ORGANIC CHEMISTRY????
Appears in Collections:	[Graduate Institute of Chemistry] journal & Dissertation

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