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  • Highly enantioselective synthesis of cyclopropylamine derivatives via Ru(II)-pheox-catalyzed direct asymmetric cyclopropanation of vinylcarbamates.

Highly enantioselective synthesis of cyclopropylamine derivatives via Ru(II)-pheox-catalyzed direct asymmetric cyclopropanation of vinylcarbamates.

Organic letters (2013-01-31)
Soda Chanthamath, Dao Thi Nguyen, Kazutaka Shibatomi, Seiji Iwasa
ZUSAMMENFASSUNG

The Ru(II)-Pheox-catalyzed asymmetric cyclopropanation of vinylcarbamates with diazoesters resulted in the corresponding cyclopropylamine derivatives in high yield and excellent diastereoselectivity (up to 96:4) and enantioselectivity (up to 99% ee).

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Cyclopropylamin, 98%