Synfacts 2011(8): 0899-0899  
DOI: 10.1055/s-0030-1260843
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart ˙ New York

Chiral Lewis Base Assisted Brønsted Acids

Contributor(s): Benjamin List, Ilija Čorić
A. Sakakura, M. Sakuma, K. Ishihara*
Nagoya University, Japan
Further Information

Publication History

Publication Date:
20 July 2011 (online)

Significance

Chiral phosphonium salts such as fluorosulfonate A were designed as a novel class of cationic Brønsted acid catalysts. These catalysts are formed in situ by mixing a chiral phosphorus(III) Lewis base (e.g. 1) with an achiral strong Brønsted acid (e.g. FSO3H) and are termed ‘chiral Lewis base assisted Brønsted acids’ (chiral LBBAs). Brønsted acid A was found to catalyze the enantioselective cyclization of 2-geranylphenols 2 to give the desired trans-fused cyclized products 3 with generally moderate to good dia­stereo- and enantioselectivities. However, high enantioselectivity could also be achieved (er up to 96.5:3.5).