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

Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/24206

標題:	1, 3-Dipolar Cycloaddition of Azomethine Ylides as A Platform for Diversity-Oriented and Target-Oriented Syntheses of Biologically Active Compounds
作者:	Konstantin V. Kudryavtsev
日期:	2011
上傳時間:	2011-06-23 14:57:01 (UTC+8)
摘要:	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].
關聯:	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:	[藥理學院] 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會

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