Issue 35, 2017

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

Abstract

The first organocatalytic asymmetric reaction of acyclic enecarbamates 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.

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

Supplementary files

Article information

Article type
Communication
Submitted
18 Jul 2017
Accepted
22 Aug 2017
First published
22 Aug 2017

Org. Biomol. Chem., 2017,15, 7272-7276

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

C. Gharui, S. Singh and S. C. Pan, Org. Biomol. Chem., 2017, 15, 7272 DOI: 10.1039/C7OB01766A

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