1, 3-Dipolar Cycloaddition of Azomethine Ylides as A Platform for Diversity-Oriented and Target-Oriented Syntheses of Biologically Active Compounds

CNU IR > Pharmacy and Science > 2011 Taiwanese-Russian Organic, Medicinal and Bio Chemistry Interactions & PST Medicinal Chemistry Symposium > Item 310902800/24206

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Title:	1, 3-Dipolar Cycloaddition of Azomethine Ylides as A Platform for Diversity-Oriented and Target-Oriented Syntheses of Biologically Active Compounds
Authors:	Konstantin V. Kudryavtsev
Date:	2011
Issue Date:	2011-06-23 14:57:01 (UTC+8)
Abstract:	1,3-Dipolar c cycloaddition of azomethine ylides is an efficient strategy for the synthesis of pyrrolidine derivatives with formation of up to four new stereogenic centers in a single synthetic step. Application of flinctionalized pyrrolidines towards diversity (scheme 1) and target (scheme 2) syntheses will be discussed in the report based on the author's works [1-9].
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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