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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
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
L-Pipecolsäure, 99% (titration)
Sigma-Aldrich
Pipecolinsäure, 98%