4.8 Article

Harnessing the beta-Silicon Effect for Regioselective and Stereoselective Rhodium(II)-Catalyzed C-H Functionalization by Donor/Acceptor Carbenes Derived from 1-Sulfony1-1,2,3-triazoles

Journal

ORGANIC LETTERS
Volume 20, Issue 8, Pages 2168-2171

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.8b00427

Keywords

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Funding

  1. NIH [GM099142]
  2. AbbVie
  3. National Science Foundation [CHE 1531620, CHE 1626172]
  4. Division Of Chemistry [1531620] Funding Source: National Science Foundation
  5. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM099142] Funding Source: NIH RePORTER

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The regioselective and enantioselective intermolecular sp(3) C-H functionalization of silicon-substituted alkanes was accomplished using Rh-2(S-NTTL)(4) with readily available 1-sulfonyl-1,2,3-triazoles as carbene precursors. These reactions generate a diverse array of stereodefined substituted silaalkanes.

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