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February 17, 2026

Markovnikov-Selective Hydroboration of Unactivated Alkenes via MHAT under Cobalt/Photoredox Dual Catalysis

Key Points

To develop a method for Markovnikov-selective hydroboration of unactivated alkenes using dual catalysis.
Employ Markovnikov-selective hydroboration using MHAT
Utilize cobalt and photoredox dual catalysis
Investigate the reaction across mono-, di-, and trisubstituted alkenes
Achieve high regioselectivity in hydroboration
Generate alkyl boronic esters from unactivated alkenes
Utilize radical intermediates to facilitate the reaction

Abstract

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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Authors

Yusuke Seino

Hokkaido University

Shintaro Dozen

Kyoto University

Tatsuhiko Yoshino

Kyoto University

Journals

Organic Letters

Actions

Institutions

Kyoto University

Hokkaido University

Graduate School USA

References and Citations

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Building similarity graph...

Analyzing shared references across papers

Markovnikov-Selective Hydroboration of Unactivated Alkenes via MHAT under Cobalt/Photoredox Dual Catalysis

Key Points

Abstract

Citation Network

Connected Papers

Discussion

Authors

Journals

Actions

Institutions

References and Citations

Citation Network

Connected Papers

Discussion

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