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Updated: Dec 16, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Radical-Induced 1,2-Migrations of Boron Ate Complexes
Marvin Kischkewitz1, Florian W Friese1, Armido Studer1
1Organisch-Chemisches Institut Westfälische Wilhelms-Universität Corrensstrasse 40 48149 Münster Germany.
Abstract:
1,2-Boron ate rearrangements represent a fundamental class of transformations to establish new C-C bonds while retaining the valuable boron moiety in the product. In established ionic processes, the boron ate complex is activated by an external electrophile to induce a 1,2-migration from boron to an adjacent sp 3 or sp 2 carbon atom. Recently, two complementary radical polar crossover approaches have been explored for both classes, 1,2-migrations to sp 2 and sp 3 carbon centers. This review describes the general concepts in this emerging research field and summarizes recent developments of radical-induced 1,2-migrations from boron to carbon.
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