Low-valent cobalt catalyzed direct dehydroxylative cross-coupling of benzyl alcohols with aryl-chlorides.
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ABSTRACT: The direct functionalization of alcohols via C-O bond cleavage is a synthetically valuable but challenging transformation. In this work, we report a reductive C(sp3)-C(sp2) cross-coupling reaction between benzyl alcohols and a broad range of aryl chlorides. The success of this transformation is attributed to the development of low-coordinate cobalt/bipyridine complexes, which enable the selective conversion of benzyl alcohols into the corresponding diarylmethanes, while minimizing undesired homocoupling of either the benzyl alcohol or aryl chlorides.
SUBMITTER: Shinde PS
PROVIDER: S-EPMC12606466 | biostudies-literature | 2026 Jan
REPOSITORIES: biostudies-literature
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