Enantiospecific synthesis of 3,4-disubstituted glutamic acids via controlled stepwise ring-opening of 2,3-aziridino-γ-lactone
暂无分享,去创建一个
[1] M. Oba,et al. A concise diastereoselective synthesis of (2S,3S,4R)-3,4-dihydroxyglutamic acid , 2001 .
[2] P. Dauban,et al. A new straightforward synthesis of 2,3-aziridino-γ-lactones , 2000 .
[3] L. Prézeau,et al. First enantiospecific synthesis of a 3,4-dihydroxy-L-glutamic acid [(3S,4S)-DHGA], a new mGluR1 agonist. , 2000, Bioorganic & medicinal chemistry letters.
[4] N. Langlois. Short stereocontrolled synthesis of (2S,3S,4R)-3,4-dihydroxyglutamic acid , 1999 .
[5] P. Dauban,et al. Application of 2,3-aziridino-γ-lactone methodology toward the enantiospecific synthesis of the (3S,4S)-isomer of dihydroxy-L-glutamic acid , 1999 .
[6] G. Shapiro,et al. Facile and Selective O-Alkyl Transesterification of Primary Carbamates with Titanium(IV) Alkoxides. , 1997, The Journal of organic chemistry.
[7] P. Dauban,et al. Synthesis of 2,3-aziridino-2,3-dideoxy-D-lyxono-γ-lactone 5-phosphonate from D-ribose, a new member of the 2,3-aziridino-γ-lactone family of synthons , 1997 .
[8] P. Dauban,et al. 2,3-Aziridino-2,3-dideoxy-D-ribono-gamma-lactone 5-Phosphonate: Stereocontrolled Synthesis from D-Lyxose and Unusual Aziridine Ring Opening. , 1997, The Journal of organic chemistry.
[9] P. Dauban,et al. Reactivity of 2,3-Aziridino-2,3-dideoxy-D-lyxono-.gamma.-lactone Derivatives, Rigid Analogs of Aziridine-2-carboxylic Esters, toward Soft and Hard Nucleophiles: Control of Lactone vs Aziridine Ring Opening and C-2 vs C-3 Regioselectivity , 1995 .
[10] R. Dodd,et al. Preparation of .beta.-substituted tryptophan derivatives: comparison of the reactivity of N-methylindole toward aziridine-2-lactones and aziridine-2-carboxylic esters and interpretation of results using MNDO calculations , 1994 .
[11] R. Dodd,et al. Stereocontrolled synthesis of aziridine-2-lactones from d-ribose and d-lyxose , 1993 .