论文信息 - Asymmetric synthesis of unusual amino acids : An enantioselective synthesis of the four isomers of D- and L-O-Methyl-2′, β-Dimethyltyrosine - 字舞流文

Asymmetric synthesis of unusual amino acids : An enantioselective synthesis of the four isomers of D- and L-O-Methyl-2′, β-Dimethyltyrosine

V. Hruby | Guigen Li | M. Jarosinski | K. Russell

[1] Chi-Cheng Wu,et al. Lewis acid promoted asymmetric 1,4-addition of allyltrimethylsilanes to chiral α,β-unsaturated n-acylamides , 1992 .

[2] V. Hruby,et al. Topographic design of peptide neurotransmitters and hormones on stable backbone templates: relation of conformation and dynamics to bioactivity , 1991 .

[3] Davidr . Evans,et al. The asymmetric synthesis of .alpha.-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-.alpha.-azido carboxylic acids , 1990 .

[4] Davidr . Evans,et al. Electrophilic azide transfer to chiral enolates. A general approach to the asymmetric synthesis of .alpha.-amino acids , 1987 .

[5] W. Oppolzer,et al. Asymmetric syntheses of α-amino acids from α-halogenated 10-sulfonamido-isobornyl esters. , 1986 .