Stereoselective Synthesis of β-Substituted Phenylalanine-β-phenylisoserine-Derived Tripeptides Using N-Cinnamoyl-l-proline as Template: Synthesis of Structural Analogues of HIV Protease Inhibitors

Biswajit Saha,Jyoti Prokash Nandy,Shalini Shukla,Iffat Siddiqui,Javed Iqbal

Stereoselective Synthesis of β-Substituted Phenylalanine-β-phenylisoserine-Derived Tripeptides Using N-Cinnamoyl-l-proline as Template: Synthesis of Structural Analogues of HIV Protease Inhibitors

2002

Biswajit Saha
Jyoti Prokash Nandy
Shalini Shukla
Iffat Siddiqui
Javed Iqbal

N-Cinnamoyl-L-proline can be used as a template on which β-substituted phenylalanine and β-phenylisoserine residues can be synthesized leading to tripeptide derivatives as structural analogues of HIV protease inhibitors.

Keywords:

HIV Protease Inhibitor
Epoxide
Enantioselective synthesis
Chemical synthesis
Phenylalanine
Organic chemistry
Proline
Tripeptide
Chemistry
Stereoselectivity
Stereochemistry

Correction
Source
Cite
Save
Machine Reading By IdeaReader

References

Citations