A method for transition metal-free 1,2-carboboration of unactivated alkenes with bis(catecholato)diboron as the boron source in combination with alkyl halides as the alkyl component is introduced. The three-component reaction proceeds via a radical pathway on a broad range of unactivated alkenes, and the 1,2-carboboration products serve as valuable synthetic building blocks. Density functional theory calculations provide insights into the mechanism.
Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes
Ying Cheng,Christian Mück‐Lichtenfeld,A. Studer
Published 2018 in Journal of the American Chemical Society
ABSTRACT
PUBLICATION RECORD
- Publication year
2018
- Venue
Journal of the American Chemical Society
- Publication date
2018-05-09
- Fields of study
Medicine, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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