Radical Fragment Coupling Route to Geminal Bis(boronates)

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)5304-5308
Number of pages5
JournalOrganic Letters
Volume20
Issue number17
DOIs
Publication statusPublished - 7 Sept 2018
Externally publishedYes

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