The synthesis of a novel and versatile (2S,5S)-2,5-bis-[(1,1'-dimethylethoxy)carbonylamino]-1,6-diphenylhex-3-ene (2) based on Julia's olefination strategy coupled with its application in stereoselective preparations of HIV protease inhibitors has been discussed
HIV-1 protease binds to its peptide/protein substrates in extended conformations. Therefore protease...
The addition of gamma-monosubstituted allylchromium(lll) reagents to N-protected alpha-amino aldehyd...
Peptidomimetic inhibitors of HIV-1 PR are still a key resource in the fight against AIDS. Here we de...
A new protocol is described for the stereocontrolled synthesis of pseudo-C2-symmetric core units of ...
Substituted bis-THF containing protease inhibitors were designed to optimize ligand-enzyme interacti...
Human Immunodeficiency Virus (HIV) is the causative agent of Acquired Immune Deficiency Syndrome (AI...
2-Substituted 3-(trimethylsilyl)-1-propenes react with N-Boc-alpha-amino aldehydes in the presence o...
In an effort to identify a new class of druglike HIV-1 protease inhibitors, four different stereopur...
As part of our studies directed toward the development of new HIV protease inhibitors, a new type of...
C2 symmetric and non-symmetric pseudopeptide inhibitors of HIV-1 protease, containing a S,S,S,S-diam...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
C2 symmetric and non-symmetric pseudopeptide inhibitors of HIV-1 protease, containing a S,S,S,S-diam...
N-Cinnamoyl-L-proline can be used as a template on which β-substituted phenylalanine and β...
HIV-1 protease inhibitors are important in the most frequently used regimen for the treatment of HIV...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...
HIV-1 protease binds to its peptide/protein substrates in extended conformations. Therefore protease...
The addition of gamma-monosubstituted allylchromium(lll) reagents to N-protected alpha-amino aldehyd...
Peptidomimetic inhibitors of HIV-1 PR are still a key resource in the fight against AIDS. Here we de...
A new protocol is described for the stereocontrolled synthesis of pseudo-C2-symmetric core units of ...
Substituted bis-THF containing protease inhibitors were designed to optimize ligand-enzyme interacti...
Human Immunodeficiency Virus (HIV) is the causative agent of Acquired Immune Deficiency Syndrome (AI...
2-Substituted 3-(trimethylsilyl)-1-propenes react with N-Boc-alpha-amino aldehydes in the presence o...
In an effort to identify a new class of druglike HIV-1 protease inhibitors, four different stereopur...
As part of our studies directed toward the development of new HIV protease inhibitors, a new type of...
C2 symmetric and non-symmetric pseudopeptide inhibitors of HIV-1 protease, containing a S,S,S,S-diam...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
C2 symmetric and non-symmetric pseudopeptide inhibitors of HIV-1 protease, containing a S,S,S,S-diam...
N-Cinnamoyl-L-proline can be used as a template on which β-substituted phenylalanine and β...
HIV-1 protease inhibitors are important in the most frequently used regimen for the treatment of HIV...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...
HIV-1 protease binds to its peptide/protein substrates in extended conformations. Therefore protease...
The addition of gamma-monosubstituted allylchromium(lll) reagents to N-protected alpha-amino aldehyd...
Peptidomimetic inhibitors of HIV-1 PR are still a key resource in the fight against AIDS. Here we de...