Nickel-catalyzed 1,2-carboboration of alkenes is emerging as a useful method for chemical synthesis. Prior studies have been limited to only the incorporation of aryl groups. In this manuscript, a method for the 1,2-benzylboration of unactivated alkenes is presented. The reaction combines readily available alkenes, diboron reagents and benzylchlorides to generate synthetically versatile products with control of stereochemistry. The utility of the products as well as the mechanistic details of the process are also presented.
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Molecular Structures and Microwave Spectra of the Gas-Phase Homodimers of 3-Fluoro-1,2-epoxypropane and 3,3-Difluoro-1,2-epoxypropane
- Award ID(s):
- 1856637
- PAR ID:
- 10438197
- Date Published:
- Journal Name:
- The Journal of Physical Chemistry A
- Volume:
- 127
- Issue:
- 30
- ISSN:
- 1089-5639
- Page Range / eLocation ID:
- 6267 to 6274
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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