Stereoselective Synthesis of HIV-1 Protease Inhibitor, DMP 323-Reference-Cited by-同舟云学术

Stereoselective Synthesis of HIV-1 Protease Inhibitor, DMP 323

Published:1996-01-01 Issue:2 Volume:61 Page:444-450
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pierce Michael E.¹,Harris Gregory D.¹,Islam Qamrul¹,Radesca Lilian A.¹,Storace Louis¹,Waltermire Robert E.¹,Wat Ed¹,Jadhav Prabhakar K.¹,Emmett George C.¹

Affiliation:

1. Chemical Proces R&D Department, Process Research Facility, The DuPont Merck Pharmaceutical Company, Deepwater, New Jersey 08023-0999, and Chemical & Physical Sciences Department, The DuPont Merck Pharmaceutical Company, Experimental Station, Wilmington, Delaware 19880-0500

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo951847u

Reference32 articles.

1. In vitro anti-human immunodeficiency virus (HIV) activity of XM323, a novel HIV protease inhibitor

2. Synthesis of C2-symmetric HIV-1 protease inhibitors from D-mannitol

3. Dipeptide isosteres. 1. Synthesis of dihydroxyethylene dipeptide isosteres via diastereoselective additions of alkyllithium reagents to N,N-dimethylhydrazones. Preparation of renin and HIV-1 protease inhibitor transition-state mimics

4. A Practical Synthesis of Nonpeptide Cyclic Ureas as Potent HIV Protease Inhibitors

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