4.8 Article

Highly Enantioselective Hydrogenative Desymmetrization of Bicyclic Imides Leading to Multiply Functionalized Chiral Cyclic Compounds

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 132, Issue 33, Pages 11414-11415

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja105048c

Keywords

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Funding

  1. MEXT [16750073, 18065007]
  2. Asahi Glass Foundation
  3. Grants-in-Aid for Scientific Research [18065007, 22225004, 16750073] Funding Source: KAKEN

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Highly enantioselective hydrogenative desymmetrization of bicyclic imides has been developed with chiral (CpRu)-Ru-star(PN) catalysts. The present hydrogenation directly provides stereochemically well-defined cyclic compounds with excellent enantiomeric exessses, which might otherwise require a detour to reach.

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