Synfacts 2009(5): 0566-0566  
DOI: 10.1055/s-0029-1216580
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart ˙ New York

Enantioselective Benzoyloxylation of Aldehydes

Contributor(s): Benjamin List, Steffen Müller
T. Kano, H. Mii, K. Maruoka*
Kyoto University, Japan
Further Information

Publication History

Publication Date:
22 April 2009 (online)

Significance

Maruoka and co-workers report the direct asymmetric benzoyloxylation of aldehydes with benzoyl peroxide using 2-tritylpyrrolidine as efficient catalyst. Catalytic amounts of hydroqui-none were found to be crucial for increased yields. The authors discuss two mechanisms, one involving the N-benzoylation of the enamine intermediate followed by a 1,3-rearrangement (path A). ­Another possible mechanism proceeds via direct C-O bond formation between enamines and benzoyl peroxide (path B).