Catalytic Markovnikov-selective hydroboration of unactivated alkenes is a powerful tool for accessing alkyl boronic esters. Here, we report Markovnikov-selective MHAT hydroboration of unactivated alkenes enabled by cobalt/photoredox dual catalysis. The reaction proceeded via radical intermediates, providing high regioselectivity with mono-, di-, and trisubstituted alkenes.
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Seino et al. (Sun,) studied this question.
www.synapsesocial.com/papers/699405bb4e9c9e835dfd692e — DOI: https://doi.org/10.1021/acs.orglett.6c00348
Yusuke Seino
Shintaro Dozen
Tatsuhiko Yoshino
Organic Letters
Kyoto University
Hokkaido University
Graduate School USA
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