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Catalytic [4+2] Cyclization of α,β-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles: Highly Diastereo- and Enantioselective Synthesis of Spirocarbocyclic Oxindoles

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Volume 52, Issue 2, Pages 585-588

Publisher

WILEY-V C H VERLAG GMBH

DOI: 10.1002/anie.201207405

Keywords

acyl chlorides; cyclization; enantioselectivity; spiro compounds

Funding

Ministry of Science and Technology of China [2011CB808600]
National Natural Science Foundation of China [21072195]
Chinese Academy of Sciences

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Catalytic [4+2] Cyclization of α,β-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles: Highly Diastereo- and Enantioselective Synthesis of Spirocarbocyclic Oxindoles

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ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Publisher

WILEY-V C H VERLAG GMBH

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Catalytic [4+2] Cyclization of α,β-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles: Highly Diastereo- and Enantioselective Synthesis of Spirocarbocyclic Oxindoles

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Publisher

WILEY-V C H VERLAG GMBH

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Funding

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