Application of the Evans aziridination procedure to 2-substituted acrylates and cinnamates: An expedient route to α-substituted α- and β-amino acids

[1]  P. Ornstein,et al.  2-Substituted (2SR)-2-amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 1. Effects of alkyl, arylalkyl, and diarylalkyl substitution. , 1998, Journal of medicinal chemistry.

[2]  P. Andersson,et al.  PREPARATION AND EVALUATION OF NITRENE PRECURSORS (PHI=NSO2AR) FOR THE COPPER-CATALYZED AZIRIDINATION OF OLEFINS , 1997 .

[3]  H. Takada,et al.  CATALYTIC ASYMMETRIC SULFIMIDATION , 1997 .

[4]  P. Reider,et al.  Nosylaziridines: Activated aziridine electrophiles , 1997 .

[5]  J. Sweeney,et al.  The asymmetric synthesis of aziridines , 1997 .

[6]  T. Wirth New Strategies to a-Alkylated a-Amino Acids. , 1997 .

[7]  D. Horwell,et al.  Regioselective nucleophilic ring opening reactions of 2,2-disubstituted aziridines — the asymmetric synthesis of α,α-disubstituted amino acids , 1996 .

[8]  F. A. Davis,et al.  2-Methyl N-(p-toluenesulfinyl)aziridine-2-carboxylic acid: Asymmetric synthesis of α-methylphenylalanine and α-methyl-β-phenylserine , 1996 .

[9]  M. Cheung,et al.  3- AND 4-NITROBENZENESULFONAMIDES : EXCEPTIONALLY VERSATILE MEANS FOR PREPARATION OF SECONDARY AMINES AND PROTECTION OF AMINES , 1995 .

[10]  D. Horwell,et al.  The development of a novel series of non-peptide tachykinin NK3 receptor selective antagonists , 1995 .

[11]  Chris P. Miller,et al.  A new synthesis of α-methylserine by nucleophilic ring-opening of N-sulfonyl aziridines☆ , 1995 .

[12]  H. Shao,et al.  A New Asymmetric Synthesis of .alpha.-Methylcysteines via Chiral Aziridines , 1995 .

[13]  P. Keitz,et al.  Design and Synthesis of a Conformationally Restricted Cysteine Protease Inhibitor , 1994 .

[14]  R. L. Parsons,et al.  Total Synthesis of (-)-Thiangazole, a Naturally-Occurring HIV-1 Inhibitor , 1994 .

[15]  M. Faul,et al.  Development of the Copper-Catalyzed Olefin Aziridination Reaction , 1994 .

[16]  G. Pattenden,et al.  Synthesis of the thiazoline-based siderophore (S)-desferrithiocin , 1993 .

[17]  Zhen Li,et al.  Asymmetric alkene aziridination with readily available chiral diimine-based catalysts , 1993 .

[18]  M. Faul,et al.  Bis(oxazoline)-copper complexes as chiral catalysts for the enantioselective aziridination of olefins , 1993 .

[19]  H. Shirahama,et al.  New amino acids from the poisonous mushroom clitocybe acromelalga , 1992 .

[20]  R. Lowenthal,et al.  Asymmetric copper-catalyzed cyclopropanation of trisubstituted and unsymmetrical cis-1,2-disubstituted olefins: modified bis-oxazoline ligands , 1991 .

[21]  J. Hunter,et al.  Rationally designed "dipeptoid" analogues of CCK. alpha-Methyltryptophan derivatives as highly selective and orally active gastrin and CCK-B antagonists with potent anxiolytic properties. , 1991, Journal of medicinal chemistry.

[22]  K. V. Rowsell,et al.  The chemistry and biochemistry of the amino acids : Edited by G.C. Barrett Chapman and Hall; London, 1985 x + 684 pages. £49.50 (hardback) , 1987 .