Journal
ORGANIC LETTERS
Volume 19, Issue 24, Pages 6590-6593Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b03296
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Funding
- China Scholarship Council
- Swedish Research Council
- Knut and Alice Wallenberg Foundation
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This communication describes an efficient palladium pincer complex-catalyzed allylic C-H borylation of alkenes. The transformation exhibits high regio- and stereo selectivity with a variety of linear alkenes. A synthetically useful feature of this allylic C-H borylation method is that all allyl-Bpin products can be isolated in usually high yields. Preliminary mechanistic studies indicate that this CH borylation reaction proceeds via Pd(IV) pincer complex intermediates.
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