Enantioselective C-C Bond Formation Promoted By Camphor-Derived Chiral Ligands

CNU IR > Pharmacy and Science > 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium > Item 310902800/24202

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Title:	Enantioselective C-C Bond Formation Promoted By Camphor-Derived Chiral Ligands
Authors:	Biing-Jiun Uang (汪炳鈞)
Date:	2011
Issue Date:	2011-06-23 14:56:58 (UTC+8)
Abstract:	Chiral alcohols are important compounds that either show biological activity or are key intermediates for natural product synthesis. The design of novel reactions that proceed with high atom economy and enable multiple transformations through a shorter reaction sequence is an integral part of modern organic synthesis. The utility of chiral ligands in catalytic eenantioselective C-C bond formation is amply demonstrated in a myriad of organic transformations. We have studied the ability of new camphor derived chiral ligands in asymmetric catalysis and found that high enantioselectivities were obtained in the enantioselective C-C bond formation reactions. The results of enantioselective addition of silylcyanide, and organozinc reagents to aldehydes will be presente.
Relation:	2011年台俄有機、藥物與生物化學交流暨藥物化學研討會，起迄日：2011/04/06~2011/04/05，地點：溪頭台大實驗林
Appears in Collections:	[Pharmacy and Science] 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium

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