Issue 56, 2014

Enantioselective Prins cyclization: BINOL-derived phosphoric acid and CuCl synergistic catalysis

Abstract

The first catalytic enantioselective Prins cyclization is disclosed. The reaction is catalyzed by the combination of a chiral BINOL-derived bis-phosphoric acid and CuCl. The process consists of a tandem Prins/Friedel–Crafts cyclization that affords the hexahydro-1H-benzo[f]isochromenes products with three new contiguous stereogenic centers in high yields, and good enantio- and excellent diastereoselectivities.

Graphical abstract: Enantioselective Prins cyclization: BINOL-derived phosphoric acid and CuCl synergistic catalysis

Supplementary files

Article information

Article type
Communication
Submitted
16 Apr 2014
Accepted
11 May 2014
First published
22 May 2014

Chem. Commun., 2014,50, 7495-7498

Author version available

Enantioselective Prins cyclization: BINOL-derived phosphoric acid and CuCl synergistic catalysis

C. Lalli and P. van de Weghe, Chem. Commun., 2014, 50, 7495 DOI: 10.1039/C4CC02826K

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