Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632-Reference-Cited by-同舟云学术

Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632

Published:2002-04-20 Issue:3 Volume:6 Page:323-328
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Xu Zhongmin¹,Singh Janak¹,Schwinden Mark D.¹,Zheng Bin¹,Kissick Thomas P.¹,Patel Bharat¹,Humora Michael J.¹,Quiroz Fernando¹,Dong Lin¹,Hsieh Dau-Ming¹,Heikes James E.¹,Pudipeddi Madhusudhan¹,Lindrud Mark D.¹,Srivastava Sushil K.¹,Kronenthal David R.¹,Mueller Richard H.¹

Affiliation:

1. The Bristol-Myers Squibb Pharmaceutical Research Institute, Process Research and Development, P.O. Box 4000, Princeton, New Jersey 08543, U.S.A., Process Research and Development, P.O. Box 191, New Brunswick, New Jersey 08903, U.S.A. and Biopharmaceutics Research and Development, P.O. Box 191, New Brunswick, New Jersey 08903, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op025504r

Reference24 articles.

1. Aza-Peptide Analogs as Potent Human Immunodeficiency Virus Type-1 Protease Inhibitors with Oral Bioavailability

2. New Aza-Dipeptide Analogues as Potent and Orally Absorbed HIV-1 Protease Inhibitors: Candidates for Clinical Development

3. In Vitro Resistance Profile of the Human Immunodeficiency Virus Type 1 Protease Inhibitor BMS-232632

4. BMS-232632, a Highly Potent Human Immunodeficiency Virus Protease Inhibitor That Can Be Used in Combination with Other Available Antiretroviral Agents

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