4.8 Article

Radical Fragment Coupling Route to Geminal Bis(boronates)

Journal

ORGANIC LETTERS
Volume 20, Issue 17, Pages 5304-5308

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b02235

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Funding

  1. Ecole Polytechnique

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The radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and related alkenes occurs without complications from fragmentation or hydrogen atom abstraction and delivers a vast array of highly functional geminal bis(boronates). The ability to assemble geminal bis(boronates) bearing polar functional groups not readily obtained through existing methods is particularly noteworthy. This approach also opens up access to geminal bis(boronyl) cyclopropanes and geminal bis(boronyl) tetrahydroquinolines.

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