Facile syntheses of aryldifluorophosphonate building blocks

[1]  S. Shibuya,et al.  Enzymatic desymmetrization of prochiral 2-benzyl-1,3-propanediol derivatives: A practical chemoenzymatic synthesis of novel phosphorylated tyrosine analogues , 1998 .

[2]  Scott D. Taylor,et al.  Naphthalenebis[α,α-difluoromethylenephosphonates] as potent inhibitors of protein tyrosine phosphatases , 1998 .

[3]  J. Urban,et al.  A FACILE SOLUTION AND SOLID PHASE SYNTHESIS OF PHOSPHOTYROSINE MIMETIC L-4-DIETHYLPHOSPHONO(DIFLUOROMETHYL)-PHENYLALANINE (F2PMP(ETO)2) DERIVATIVES , 1997 .

[4]  B. Stec,et al.  The road less travelled: taming phosphatases. , 1997, Chemistry & biology.

[5]  S. Shibuya,et al.  Facile synthesis of aryl(difluoromethyl)phosphonates through CuBr-mediated cross coupling reactions of [(diethoxyphosphinyl)difluoromethyl]zinc bromide with aryl iodides , 1997 .

[6]  W. Qiu,et al.  A facile and general preparation of α,α-difluoro benzylic phosphonates by the CuCl promoted coupling reaction of the (diethylphosphonyl)difluoromethylcadmium reagent with aryl lodides , 1996 .

[7]  D. Solas,et al.  An Efficient Synthesis of N-α-Fmoc-4-(Phosphonodifluoromethyl)-l- phenylalanine , 1996 .

[8]  A. Saltiel,et al.  Targeting signal transduction in the discovery of antiproliferative drugs. , 1996, Chemistry & biology.

[9]  S. Shoelson,et al.  Nonhydrolyzable phosphotyrosyl mimetics for the preparation of phosphatase-resistant SH2 domain inhibitors. , 1994, Biochemistry.

[10]  T. Burke,et al.  Enantioselective synthesis of N-boc and N-fmoc protected diethyl 4-phosphono(difluoromethyl)-L-phenylalanine; agents suitable for the solid-phase synthesis of peptides containing nonhydrolyzable analogues of O-phosphotyrosine , 1994 .

[11]  K. James,et al.  Preparation of enantiomerically pure protected 4-oxo .alpha.-amino acids and 3-aryl .alpha.-amino acids from serine , 1992 .

[12]  A. Echavarren,et al.  Palladium-catalyzed coupling of aryl triflates with organostannanes , 1987 .