Abstract
A copper-catalyzed conjugate addition of alkylboron compounds (alkyl-9-BBN, prepared by hydroboration of alkenes with 9-BBN-H) to alkynoates to form β-disubstituted acrylates is reported. The addition occurred in a formal syn-hydroalkylation mode. The syn stereoselectivity was excellent regardless of the substrate structure. A variety of functional groups were compatible with the conjugate addition.
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Wakamatsu, T., Nagao, K., Ohmiya, H., & Sawamura, M. (2015). Copper-catalyzed stereoselective conjugate addition of alkylboranes to alkynoates. Beilstein Journal of Organic Chemistry, 11, 2444–2450. https://doi.org/10.3762/bjoc.11.265
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