The discovery and development of an efficient, practical asymmetric synthesis of the HIV Protease inhibitor CRIXIVAN® is described. Particular emphasis is placed on the selective installation of each of the five stereogenic centers as well as design strategies associated with the preparation of a complex pharmaceutical agent needed in multiton quantities
A thesis submitted to the Faculty of Science University of the Witwatersrand Johannesburg in fulfil...
Organic chemistry is an exploratory world in which chemists translate their knowledge by creating ne...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...
Enantioselective total synthesis of the recently isolated, novel polyketide natural product (+)-inte...
Since the emergence of AIDS in the early 1980s, strategies to mitigate the disease remain a high pri...
This study has focused on the synthesis of truncated analogues of the hydroxyethylene dipeptide isos...
An asymmetric total synthesis of the aminocyclopentitol pactamycin is described, which delivers the ...
Peptidomimetic HIV protease inhibitors are an important class of drugs used in the treatment of AIDS...
Viral infections cause many severe human diseases, being responsible for remarkably high mortality r...
Harnessing the power of process intensification principles in a robust synthesis of the anti-retrovi...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
A novel and efficient route to asymmetric synthesis of Maraviroc by using (S)-tert-butanesulfinamide...
I. Asymmetric Synthesis of the Aminocyclitol Pactamycin, a Universal Translocation Inhibitor A conci...
The authors thank the Royal Society for a URF (ADS), Cancer Research UK (ER), the Leverhulme Trust (...
Efficient synthetic routes were developed to prepare a sizable amount (4-15 grams) of the chiral epo...
A thesis submitted to the Faculty of Science University of the Witwatersrand Johannesburg in fulfil...
Organic chemistry is an exploratory world in which chemists translate their knowledge by creating ne...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...
Enantioselective total synthesis of the recently isolated, novel polyketide natural product (+)-inte...
Since the emergence of AIDS in the early 1980s, strategies to mitigate the disease remain a high pri...
This study has focused on the synthesis of truncated analogues of the hydroxyethylene dipeptide isos...
An asymmetric total synthesis of the aminocyclopentitol pactamycin is described, which delivers the ...
Peptidomimetic HIV protease inhibitors are an important class of drugs used in the treatment of AIDS...
Viral infections cause many severe human diseases, being responsible for remarkably high mortality r...
Harnessing the power of process intensification principles in a robust synthesis of the anti-retrovi...
The proteolytic enzyme of the human immunodeficiency virus (HIV-PR) plays an important role in the H...
A novel and efficient route to asymmetric synthesis of Maraviroc by using (S)-tert-butanesulfinamide...
I. Asymmetric Synthesis of the Aminocyclitol Pactamycin, a Universal Translocation Inhibitor A conci...
The authors thank the Royal Society for a URF (ADS), Cancer Research UK (ER), the Leverhulme Trust (...
Efficient synthetic routes were developed to prepare a sizable amount (4-15 grams) of the chiral epo...
A thesis submitted to the Faculty of Science University of the Witwatersrand Johannesburg in fulfil...
Organic chemistry is an exploratory world in which chemists translate their knowledge by creating ne...
We have developed a conceptually new generation of non-peptidic HIV-1 protease inhibitors incorporat...