Stereoselective synthesis of beta-substituted phenylalanine-beta-phenylisoserine-derived tripeptides using N-cinnamoyl-L-proline as template: synthesis of structural analogues of HIV protease inhibitors.
Saha, Biswajit
Stereoselective synthesis of beta-substituted phenylalanine-beta-phenylisoserine-derived tripeptides using N-cinnamoyl-L-proline as template: synthesis of structural analogues of HIV protease inhibitors. [electronic resource] - The Journal of organic chemistry Nov 2002 - 7858-60 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0022-3263
10.1021/jo0109826 doi
Cinnamates--chemical synthesis
Crystallography, X-Ray
HIV Protease Inhibitors--chemical synthesis
Magnetic Resonance Spectroscopy
Models, Molecular
Molecular Conformation
Molecular Structure
Peptides--chemical synthesis
Phenylalanine--chemistry
Proline--analogs & derivatives
Serine--analogs & derivatives
Stereoisomerism
Stereoselective synthesis of beta-substituted phenylalanine-beta-phenylisoserine-derived tripeptides using N-cinnamoyl-L-proline as template: synthesis of structural analogues of HIV protease inhibitors. [electronic resource] - The Journal of organic chemistry Nov 2002 - 7858-60 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0022-3263
10.1021/jo0109826 doi
Cinnamates--chemical synthesis
Crystallography, X-Ray
HIV Protease Inhibitors--chemical synthesis
Magnetic Resonance Spectroscopy
Models, Molecular
Molecular Conformation
Molecular Structure
Peptides--chemical synthesis
Phenylalanine--chemistry
Proline--analogs & derivatives
Serine--analogs & derivatives
Stereoisomerism