Add to ORKGManickam G, Nogami H, Kanai M, Gröger H, Shibasaki M. Anti- and Syn-Selective Cyanosilylation Reactions Promoted by a Sugar-Based Bifunctional Catalyst: Stereoselective Synthesis of Essential building Blocks for HIV Protease Inhibitors and Bestatin. Synlett. 2001:617-620
A novel methodology for the synthesis of amino sugars and aza-sugars, important inhibitors of glycos...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...
A new protocol is described for the stereocontrolled synthesis of pseudo-C2-symmetric core units of ...
International audienceA key intermediate in the total synthesis of naturally occurring anti-HIV Isol...
2-Substituted 3-(trimethylsilyl)-1-propenes react with N-Boc-alpha-amino aldehydes in the presence o...
Enzymatic stereoselectivity has typically been unrivalled by most chemical catalysts, especially in ...
Substituted bis-THF containing protease inhibitors were designed to optimize ligand-enzyme interacti...
The use of palladium-catalyzed reactions to introduce new carbon-carbon bonds is a fundamental synth...
An efficient, mild and inexpensive protocol for the stereoselective construction of cyanohydrins in ...
Human Immunodeficiency Virus (HIV) is the causative agent of Acquired Immune Deficiency Syndrome (AI...
HIV-1 protease inhibitors are important in the most frequently used regimen for the treatment of HIV...
AbstractBackground: Silicon is the element most similar to carbon, and bioactive organosilanes have ...
The synthesis of a novel and versatile (2S,5S)-2,5-bis-[(1,1'-dimethylethoxy)carbonylamino]-1,6-diph...
Two new analogs of bestatin were prepared from D-leucine and D-valine in a stereoselective and effic...
A novel methodology for the synthesis of amino sugars and aza-sugars, important inhibitors of glycos...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...
A new protocol is described for the stereocontrolled synthesis of pseudo-C2-symmetric core units of ...
International audienceA key intermediate in the total synthesis of naturally occurring anti-HIV Isol...
2-Substituted 3-(trimethylsilyl)-1-propenes react with N-Boc-alpha-amino aldehydes in the presence o...
Enzymatic stereoselectivity has typically been unrivalled by most chemical catalysts, especially in ...
Substituted bis-THF containing protease inhibitors were designed to optimize ligand-enzyme interacti...
The use of palladium-catalyzed reactions to introduce new carbon-carbon bonds is a fundamental synth...
An efficient, mild and inexpensive protocol for the stereoselective construction of cyanohydrins in ...
Human Immunodeficiency Virus (HIV) is the causative agent of Acquired Immune Deficiency Syndrome (AI...
HIV-1 protease inhibitors are important in the most frequently used regimen for the treatment of HIV...
AbstractBackground: Silicon is the element most similar to carbon, and bioactive organosilanes have ...
The synthesis of a novel and versatile (2S,5S)-2,5-bis-[(1,1'-dimethylethoxy)carbonylamino]-1,6-diph...
Two new analogs of bestatin were prepared from D-leucine and D-valine in a stereoselective and effic...
A novel methodology for the synthesis of amino sugars and aza-sugars, important inhibitors of glycos...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...