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  • Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: enantioselective total synthesis of (-)-mesembrine.

Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: enantioselective total synthesis of (-)-mesembrine.

Organic letters (2012-12-06)
Qian-Qian Zhang, Jian-Hua Xie, Xiao-Hui Yang, Jian-Bo Xie, Qi-Lin Zhou
ABSTRACT

A highly efficient asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones catalyzed by chiral spiro iridium complexes for the preparation of chiral 2-substituted allylic alcohols has been developed (ee up to 99.7%). This method provides a concise route to (-)-mesembrine (34% yield, 12 steps).

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Allyl alcohol, ≥99%
Sigma-Aldrich
Allyl alcohol, ≥98.5%
Sigma-Aldrich
Allyl alcohol, ≥98.5%