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Intramolecular carbolithiation reactions for the preparation of 3-alkenylpyrrolidines
Iain Coldham,Kathy N. Price,Richard E. Rathmell
Organic & Biomolecular Chemistry Pub Date : 05/14/2003 00:00:00 , DOI:10.1039/B303670G
Abstract

Tin–lithium exchange allows the formation of α-amino-organolithium species that undergo anionic cyclization onto allylic ethers to give 3-alkenylpyrrolidines. The methodology has been applied to the synthesis of an advanced intermediate related to the natural product (–)-α-kainic acid.

Graphical abstract: Intramolecular carbolithiation reactions for the preparation of 3-alkenylpyrrolidines
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