✦ LIBER ✦

Synthesis of 7-membered cyclic oxamides: Novel HIV-1 protease inhibitors

✍ Scribed by Prabhakar K Jadhav; Hon-Wah Man

Publisher: Elsevier Science
Year: 1996
Tongue: French
Weight: 205 KB
Volume: 37
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(96)00013-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of 7-Memb

ChemInform Abstract: Synthesis of 7-Membered Cyclic Hydroxyguanidines: Novel HIV-1 Protease Inhibitors.

✍ P. K. JADHAV; F. J. WOERNER; H.-W. MAN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis of new 7-membered α-phenylthio

Synthesis of new 7-membered α-phenylthio cyclic oxamides: HIV inhibitors

✍ M. Medou; G. Priem; G. Quélever; M. Camplo; J.L. Kraus 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 200 KB

Based on the concept of bioisosterism, we report the computer design and the synthesis of original 7-membered ct-phenylthio cyclic oxamides with potent anti HIV-1 properties.

Synthesis of 8-membered cyclic sulfamide

Synthesis of 8-membered cyclic sulfamides: Novel HIV-1 protease inhibitors

✍ Prabhakar K. Jadhav; Francis J. Woerner 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 182 KB

ChemInform Abstract: Synthesis of New 7-

ChemInform Abstract: Synthesis of New 7-Membered α-Phenylthio Cyclic Oxamides: HIV Inhibitors.

✍ M. MEDOU; G. PRIEM; G. QUELEVER; M. CAMPLO; J. L. KRAUS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

Synthesis of novel steroidal inhibitors

Synthesis of novel steroidal inhibitors of HIV-1 protease

✍ James J. Harburn; Gabrielle C. Loftus; Brian A. Marples 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 1017 KB

The design and synthesis of potential steroidal HIV-1 protease inhibitors is described. Compounds derived from 11-amino-12-keto-cholanic acid derivatives show modest activity.

Synthesis of unsymmetric cyclic urea dio

Synthesis of unsymmetric cyclic urea diols, a novel class of HIV protease inhibitors

✍ Benjamin R.P. Stone; Gregory D. Harris; Reginald O. Cann; Thomas E. Smyser; Pat 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 200 KB

Unsymmetric cyclic urea diols of general structure 1 can be prepared either via an isourea derived from the symmetric diamine 2 or by the selective removal of a benzyl group from certain symmetric cyclic ureas 8, employing dissolving metal reduction.