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  • Intramolecular hydroamination of dithioketene acetals: an easy route to cyclic amino acid derivatives.

Intramolecular hydroamination of dithioketene acetals: an easy route to cyclic amino acid derivatives.

Organic letters (2010-10-16)
Hai-Chao Xu, Kevin D Moeller
ABSTRACT

Catalytic intramolecular hydroamination of dithioketene acetals was developed for the synthesis of cyclic amino acid derivatives. Triggered by the addition of a catalytical amount of n-BuLi, the reaction proceeds to give proline and pipecolic acid derivatives in excellent yields and diastereoselectivity.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Pipecolinic acid, 98%
Sigma-Aldrich
L-Pipecolic acid, 99% (titration)