跳轉至內容
Merck
  • Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and beta-proline derivatives.

Asymmetric halo-Mannich-type reaction provides access to pyrrolidines and beta-proline derivatives.

The Journal of organic chemistry (2005-09-10)
Cody Timmons, Li Guo, Junying Liu, John F Cannon, Guigen Li
摘要

[reaction: see text] A new halo-Mannich-type reaction is reported using cyclopropyl carbonyl-derived enolates and sulfonyl-protected imines. Chiral oxazolidinones auxiliaries were found to be effective for completely controlling the stereochemistry of the products. Variations in the oxazolidinone, protecting group, and imine components show this to be a quite general reaction. The initial iodo-Mannich products were found to be readily cyclized in the presence of triethylamine to afford the resulting protected pyrrolidines, which could be readily deprotected under standard conditions.

材料
產品編號
品牌
產品描述

Sigma-Aldrich
(S)-吡咯烷-3-羧酸, ≥98.0% (NT)