Phosphinic Acid‐Based C2‐Symmetrical Inhibitors of HIV‐Protease**
- 1 December 1993
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 32 (12) , 1720-1722
- https://doi.org/10.1002/anie.199317201
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Diastereo‐ and Enantioselective Synthesis of 2‐Substituted 3‐Trialkylstannylcyclohexanones by Michael Addition of Trialkylstannyllithium to Cyclohexenone SAMP HydrazoneAngewandte Chemie International Edition in English, 1993
- Diastereo- und enantioselektive Synthese von 2-substituierten 3-Trialkylstannylcyclohexanonen durch Michael-Addition von Trialkylstannyllithium an Cyclohexenon-SAMP-HydrazonAngewandte Chemie, 1993
- A symmetric inhibitor binds HIV-1 protease asymmetricallyBiochemistry, 1993
- BIOLOGICAL ACTIVITY OF AMINOPHOSPHONIC ACIDSPhosphorus, Sulfur, and Silicon and the Related Elements, 1991
- X-ray crystal structure of the HIV protease complex with L-700,417, an inhibitor with pseudo C2 symmetryJournal of the American Chemical Society, 1991
- Design, Activity, and 2.8 Å Crystal Structure of a C 2 Symmetric Inhibitor Complexed to HIV-1 ProteaseScience, 1990
- Conserved Folding in Retroviral Proteases: Crystal Structure of Synthetic HIV-1 ProteaseScience, 1989
- Phosphoranaloge von Aminosäuren II1. Synthese von α-Aminophosphonsäuren und α-Aminophosphinsäuren, ausgehend von den entsprechendenN-Acylimino-DerivatenSynthesis, 1989
- Synthesis and biological activity of some transition-state inhibitors of human reninJournal of Medicinal Chemistry, 1988
- Synthese von 1-Aminophosphonsäure-Derivaten über Acyliminophosphonsäure-EsterSynthesis, 1986