4.6 Article

Chiral phosphoric acid catalyzed enantioselective annulation of acyclic enecarbamates to in situ-generated ortho-quinone methides

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 15, Issue 35, Pages 7272-7276

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob01766a

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Funding

  1. DST-MPI partner programme

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The first organocatalytic asymmetric reaction of acyclic enecarba-mates with o-quinone methides is disclosed. BINOL-based phosphoric acid catalysts were found to be suitable for the annulation reaction. With 10 mol% of the TRIP catalyst, high yields as well as excellent diastereo- and enantioselectivities are achieved for a variety of 2,3,4-trisubstituted chroman products.

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