期刊
ACS CATALYSIS
卷 9, 期 12, 页码 11381-11385出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.9b04453
关键词
-
资金
- NIH [R35-GM1217140]
Enantioselective conjunctive cross-coupling with propargylic carbonates affords beta-boryl allenes as the reaction product. The reaction is found to proceed through the intermediacy of dimethoxyboronate complexes that are generated in situ by a strain-induced ligand exchange reaction.
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