The Synthesis of Sterically Demanding Amino Acid-Derived Cyclic Phosphonamides
- 25 October 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 65 (23) , 7913-7918
- https://doi.org/10.1021/jo005545q
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Diastereotopic Differentiation on Phosphorus Templates via the Ring-Closing Metathesis ReactionOrganic Letters, 2000
- Ring-Closing Olefin Metathesis for the Synthesis of Phosphorus Containing HeterocyclesTetrahedron, 2000
- A novel access to alicyclic phosphine oxides via ring closing metathesisTetrahedron Letters, 1999
- Inhibitors of the C2-Symmetric HIV-1 Protease: Nonsymmetric Binding of a Symmetric Cyclic Sulfamide with Ketoxime Groups in the P2/P2‘ Side ChainsJournal of Medicinal Chemistry, 1999
- Ring closing metathesis reactions on a phosphonate templateTetrahedron Letters, 1998
- Nonsymmetric P2/P2‘ Cyclic Urea HIV Protease Inhibitors. Structure−Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 AnaloguesJournal of Medicinal Chemistry, 1998
- Calculated and Experimental Low-Energy Conformations of Cyclic Urea HIV Protease InhibitorsJournal of the American Chemical Society, 1998
- De novo design, discovery and development of cyclic urea HIV protease inhibitorsDrugs of the Future, 1998
- Synthesis of 8-membered cyclic sulfamides: Novel HIV-1 protease inhibitorsTetrahedron Letters, 1995
- Regulation of MHC Class I Transport by the Molecular Chaperone, Calnexin (p88, IP90)Science, 1994