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  • Stereoselective synthesis of nipecotic acid derivatives via palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with imines.

Stereoselective synthesis of nipecotic acid derivatives via palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with imines.

Organic letters (2008-12-17)
Ryo Shintani, Masataka Murakami, Tamio Hayashi
ABSTRACT

A new synthetic method of multisubstituted nipecotic acid (piperidine-3-carboxylic acid) derivatives has been developed by way of palladium-catalyzed decarboxylative cyclization of gamma-methylidene-delta-valerolactones with imines. By employing the diethoxyphosphinoyl group as the N-protecting group for imines, the reaction proceeds smoothly with high diastereoselectivity. The products thus obtained can be further derivatized with high efficiency under simple reaction conditions.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
δ-Valerolactone, technical grade
Sigma-Aldrich
(R)-(–)-3-Piperidinecarboxylic acid, 97%
Sigma-Aldrich
(S)-(+)-3-Piperidinecarboxylic acid, 97%