4.8 Article

Enantioselective Silylation of Aliphatic C-H Bonds for the Synthesis of Silicon-Stereogenic Dihydrobenzosiloles

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 59, Issue 49, Pages 22217-22222

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202009912

Keywords

asymmetric catalysis; C(sp(3))-H silylation; dihydrobenzosiloles; hydrosilylation; silanes

Funding

  1. National Natural Science Foundation of China [21901104]
  2. Thousand Talents Program for Young Scholars
  3. Southern University of Science and Technology
  4. Shenzhen Nobel Prize Scientists Laboratory Project [C17783101]
  5. Guangdong Provincial Key Laboratory of Catalysis [2020B121201002]

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A rhodium(I)-catalyzed enantioselective silylation of aliphatic C-H bonds for the synthesis of silicon-stereogenic dihydrobenzosiloles is demonstrated. This reaction involves a highly enantioselective intramolecular C(sp(3))-H silylation of dihydrosilanes, followed by a stereospecific intermolecular alkene hydrosilylation leading to the asymmetrically tetrasubstituted silanes. A wide range of dihydrosilanes and alkenes displaying various functional groups are compatible with this process, giving access to a variety of highly functionalized silicon-stereogenic dihydrobenzosiloles in good to excellent yields and enantioselectivities.

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