Asymmetric synthesis of (3R)-alkanoyloxytetradecanoic acids-components of bacterial lipopolysaccharidesJADHAV, P. K.Tetrahedron letters. 1989, Vol 30, Num 36, pp 4763-4766, issn 0040-4039Article

B-allyldiisocaranylborane: a new, remarkable enantioselective allylborating agent for prochiral aldehydes: synthesis of homoallylic alcohols approaching 100% enantiomeric puritiesBROWN, H. C; JADHAV, P. K.Journal of organic chemistry. 1984, Vol 49, Num 21, pp 4089-4091, issn 0022-3263Article

Synthesis of C₂-symmetric HIV-1 protease inhibitors from D-mannitolJADHAV, P. K; WOERNER, F. J.Bioorganic & medicinal chemistry letters. 1992, Vol 2, Num 4, pp 353-356Article

Cyclic HIV protease inhibitors : Design and synthesis of orally bioavailable, pyrazole P2/P2' cyclic ureas with improved potencyQI HAN; CHANG, C.-H; RENHUA LI et al.Journal of medicinal chemistry (Print). 1998, Vol 41, Num 12, pp 2019-2028, issn 0022-2623Article

Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors : Synthesis, structure-activity relationships, and X-ray crystal structure studiesJADHAV, P. K; WOERNER, F. J; ERICKSON-VIITANEN, S et al.Journal of medicinal chemistry (Print). 1998, Vol 41, Num 9, pp 1446-1455, issn 0022-2623Article

The synthesis of symmetrical and unsymmetrical P1/P1' cyclic ureas as HIV protease inhibitorsPATEL, M; KALTENBACH, R. F; REID, C et al.Bioorganic & medicinal chemistry letters (Print). 1998, Vol 8, Num 9, pp 1077-1082, issn 0960-894XArticle

Cyclic urea amides : HIV-1 protease inhibitors with low nanomolar potency against both wild type and protease inhibitor resistant mutants of HIVJADHAV, P. K; ALA, P; WOERNER, F. J et al.Journal of medicinal chemistry (Print). 1997, Vol 40, Num 2, pp 181-191, issn 0022-2623Article

NMR evidence for the displacement of a conserved interior water molecule in HIV protease by a non-peptide cyclic urea-based inhibitorGRZESIEK, S; BAX, A; JADHAV, P. K et al.Journal of the American Chemical Society. 1994, Vol 116, Num 4, pp 1581-1582, issn 0002-7863Article

Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitorsLAM, P. Y. S; JADHAV, P. K; CHONG-HWAN CHANG et al.Science (Washington, D.C.). 1994, Vol 263, Num 5145, pp 380-384, issn 0036-8075Article

Enantioselective synthesis of disubstituted alkynes via organoboranesBROWN, C. A; DESAI, M. C; JADHAV, P. K et al.Journal of organic chemistry. 1986, Vol 51, Num 2, pp 162-167, issn 0022-3263Article

DMP 323, a nonpeptide cyclic urea inhibitor of human immunodeficiency virus (HIV) protease, specifically and persistently blocks intracellular processing of HIV gag polypoproteinRAYNER, M. M; CORDOVA, B. C; MEADE, R. P et al.Antimicrobial agents and chemotherapy. 1994, Vol 38, Num 7, pp 1635-1640, issn 0066-4804Article

A convenient method for upgrading the enantiomeric purities of (+)-longifolene and (+)-3-carene to materials approaching 100% eeJADHAV, P. K; VARA PRASAD, J. V. N; BROWN, H. C et al.Journal of organic chemistry. 1985, Vol 50, Num 17, pp 3203-3206, issn 0022-3263Article

A convenient method for upgrading the enantiomeric purities of (+)-longifolene and (+)-3-carene to materials approaching 100% eeJADHAV, P. K; VARA PRASAD, J. V. N; BROWN, H. C et al.Journal of organic chemistry. 1985, Vol 50, Num 17, pp 3203-3206, issn 0022-3263Article

Organoboranes. XXXIV: General synthesis of chiral boronic and borinic esters via asymmetric hydroboration-displacement. Carbenoidation of chiral borinic esters to acyclic ketones of high enantiomeric puritiesBROWN, H. C; JADHAV, P. K; DESAI, M. C et al.Tetrahedron (Oxford. Print). 1984, Vol 40, Num 8, pp 1325-1332, issn 0040-4020Article

A simple and efficient synthesis of chiral acetic acid of high optical purityKOBAYASHI, K; JADHAV, P. K; ZYDOWSKY, T. M et al.Journal of organic chemistry. 1983, Vol 48, Num 20, pp 3510-3512, issn 0022-3263Article

5-Amidinoindoles as dual inhibitors of coagulation factors IXa and XaBATT, Douglas G; QIAO, Jennifer X; MODI, Dilip P et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 21, pp 5269-5273, issn 0960-894X, 5 p.Article

Disubstituted indazoles as potent antagonists of the integrin α_vβ₃BATT, D. G; PETRAITIS, J. J; BARBERA, F. A et al.Journal of medicinal chemistry (Print). 2000, Vol 43, Num 1, pp 41-58, issn 0022-2623Article

Rapid synthesis of RGD mimetics with isoxazoline scaffolds on solid phase : Identification of αvβ3 antagonists lead compoundsROCKWELL, A. L; RAFALSKI, M; PITTS, W. J et al.Bioorganic & medicinal chemistry letters (Print). 1999, Vol 9, Num 7, pp 937-942, issn 0960-894XArticle

α_vβ₃ integrin binding affinity and specificity of SM256 in various speciesMOUSA, S. A; LORELLI, W; MOHAMED, S et al.Journal of cardiovascular pharmacology. 1999, Vol 33, Num 4, pp 641-646, issn 0160-2446Article

An assay for HIV RNA in infected cell lysates, and its use for the rapid evaluation of antiviral efficacyBACHELER, L. T; PAUL, M; OTTO, M. J et al.Antiviral chemistry & chemotherapy. 1994, Vol 5, Num 2, pp 111-121, issn 0956-3202Article

Chiral synthesis via organoboranes. XIII: A highly diastereoselective and enantioselective addition of [(Z)-γ-alkoxyallyl]diisopinocampheylboranes to aldehydesBROWN, H. C; JADHAV, P. K; BHAT, K. S et al.Journal of the American Chemical Society. 1988, Vol 110, Num 5, pp 1535-1538, issn 0002-7863Article

Chiral synthesis via organoboranes. V: Asymmetric allylboration via chiral allyldialkylboranes ― Synthesis of homoallylic alcohols with exceptionally high enantiomeric excessJADHAV, P. K; BHAT, K. S; THIRUMALAI PERUMAL, P et al.Journal of organic chemistry. 1986, Vol 51, Num 4, pp 432-439, issn 0022-3263Article