Synfacts 2011(9): 1019-1019  
DOI: 10.1055/s-0030-1260916
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart ˙ New York

Organocatalytic Trifluoromethylations

Contributor(s): Benjamin List, Manuel Mahlau
T. Furukawa, T. Nishimine, E. Tokunaga, K. Hasegawa, M. Shiro, N. Shibata*
Nagoya Institute of Technology, Japan
Further Information

Publication History

Publication Date:
19 August 2011 (online)

Significance

The research group of Shibata has developed a protocol for the efficient trifluoro­methylation of Morita-Baylis-Hillman adducts using the Ruppert-Prakash reagent (Me3SiCF3). The reaction proceeds through an addition-elimination-addition-elimination sequence or SN′/SN′ mechanism. Racemic products were obtained in good to excellent yields using DABCO (1) as catalyst. An enantioselective version of the reaction was achieved using (DHQD)2PHAL (2) as the catalyst, which gave good to excellent enantioselectivities, albeit in lower yields than in the racemic reaction.