Affiliation:
1. College of Chemistry and Material Science Shanghai Normal University 100 Guilin Road Shanghai 200234 China
2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 China
Abstract
Comprehensive SummaryTransition‐metal‐catalyzed asymmetric alkylation of aldehydes represents a straightforward strategy for the synthesis of chiral secondary alcohols. However, efficient methods using organoborons as coupling reagents are rare. Herein, we report a highly enantioselective nickel‐catalyzed alkylation reaction of aldehydes, using readily available alkylborons as nucleophiles. A wide variety of chiral secondary alcohols were prepared from commercially available aldehydes with high yields. The key to the excellent enantioselectivity and chemoselectivity was the employment of a bulky C2‐symmetric chiral NHC ligand. This protocol features excellent enantiocontrol, mild conditions, and good functional group compatibility.
Funder
National Key Research and Development Program of China
Program of Shanghai Academic Research Leader
Natural Science Foundation of Ningbo Municipality
National Natural Science Foundation of China