Palladium-catalyzed allylation of 2,2,2-trifluoroethyl phenyl sulfone, a potential 2,2,2-trifluoroethyl pronucleophile

[1]  H. Amii.  Recent Progress in Catalytic Aromatic Trifluoromethylation , 2012 .

[2]  Jinbo Hu,et al.  Palladium-catalyzed 2,2,2-trifluoroethylation of organoboronic acids and esters. , 2012, Angewandte Chemie.

[3]  Etsuko Tokunaga,et al.  Construction of Trifluoromethyl‐Bearing Quaternary Carbon Centers by Intramolecular Decarboxylative Allylation of α‐Trifluoromethyl β‐Keto Esters , 2011 .

[4]  V. Grushin,et al.  Aromatic trifluoromethylation with metal complexes. , 2011, Chemical reviews.

[5]  G. Gribble,et al.  Trifluoromethylation of aryl and heteroaryl halides , 2011 .

[6]  Jinbo Hu.  Nucleophilic, radical, and electrophilic (phenylsulfonyl)difluoromethylations , 2009 .

[7]  G. Olah,et al.  A persistent alpha-fluorocarbanion and its analogues: preparation, characterization, and computational study. , 2009, Angewandte Chemie.

[8]  I. Ojima.  Fluorine in medicinal chemistry and chemical biology , 2009 .

[9]  H. Amii,et al.  Alpha-trifluoromethylated carbanion synthons. , 2008, Accounts of chemical research.

[10]  D. Bonnet-Delpon,et al.  Bioorganic and Medicinal Chemistry of Fluorine , 2008 .

[11]  K. Kirk.  Fluorination in Medicinal Chemistry: Methods, Strategies, and Recent Developments , 2008 .

[12]  Kazuyuki Sato,et al.  Formation of quaternary carbon center with a trifluoromethyl group using a Pd-catalyzed allylation reaction. , 2007, Chemical & pharmaceutical bulletin.

[13]  G. Prakash,et al.  Selective fluoroalkylations with fluorinated sulfones, sulfoxides, and sulfides. , 2007, Accounts of chemical research.

[14]  T. Ishihara,et al.  A novel synthesis of fluorine-containing quaternary amino acid derivatives via palladium-catalyzed allylation reaction , 2005 .

[15]  Jun‐An Ma,et al.  Asymmetric fluorination, trifluoromethylation, and perfluoroalkylation reactions. , 2004, Chemical reviews.

[16]  Y. Itoh,et al.  Direct generation of Ti-enolate of alpha-CF3 ketone: theoretical study and high-yielding and diastereoselective Aldol reaction. , 2004, Journal of the American Chemical Society.

[17]  G. Prakash,et al.  Nucleophilic trifluoromethylation tamed , 2001 .

[18]  T. Kitazume,et al.  Synthetic Applications of the Carbanion with a Fluoroalkyl Group Generated by Palladium(0) Catalyst under Neutral Conditions. , 1999, The Journal of organic chemistry.

[19]  K. Yamaguchi,et al.  An efficient generation of the aluminum enolates of 1H-perfluoroalkyl ketones from 1-substituted-1-perfluoroalkenyl phosphates and their aldol reaction with aldehydes , 1990 .

[20]  K. Uneyama,et al.  Generation and chemical fate of 2,2,2-trifluoro-1-phenylsulfonylethyl carbanion. , 1989 .

[21]  T. Yokozawa,et al.  (Trifluoromethyl)ketene silyl acetal as an equivalent to the trifluoropropionic ester enolate: preparation and aldol-type reactions with acetals , 1985 .

[22]  T. Yokozawa,et al.  Convenient Preparation of Dimethyl (Trifluoromethyl)malonate and Related Compounds , 1983 .

[23]  Kiyoshi Tanaka,et al.  A Convenient Preparation of Arylthioynamines , 1977 .

[24]  Jinbo Hu,et al.  Selective fluoroalkylation of organic compounds by tackling the "negative fluorine effect". , 2012, Topics in current chemistry.