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Results: 1-9 |
Results: 9
SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A NOVEL HYDROFORMYLATION ROUTE
Authors: KALDOR SW FRITZ JE WARD JA
Citation: Sw. Kaldor et al., SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A NOVEL HYDROFORMYLATION ROUTE, Tetrahedron letters, 38(9), 1997, pp. 1509-1510
RAPID PURIFICATION OF SMALL-MOLECULE LIBRARIES BY ION-EXCHANGE CHROMATOGRAPHY
Authors: SIEGEL MG HAHN PJ DRESSMAN BA FRITZ JE GRUNWELL JR KALDOR SW
Citation: Mg. Siegel et al., RAPID PURIFICATION OF SMALL-MOLECULE LIBRARIES BY ION-EXCHANGE CHROMATOGRAPHY, Tetrahedron letters, 38(19), 1997, pp. 3357-3360
SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A UNIQUE ANTIVIRAL NUCLEOSIDE
Authors: FAUL MM HUFF BE DUNLAP SE FRANK SA FRITZ JE KALDOR SW LETOURNEAU ME STASZAK MA WARD JA WERNER JA WINNEROSKI LL
Citation: Mm. Faul et al., SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A UNIQUE ANTIVIRAL NUCLEOSIDE, Tetrahedron, 53(24), 1997, pp. 8085-8104
VIRACEPT (NELFINAVIR MESYLATE, AG1343) - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE
Authors: KALDOR SW KALISH VJ DAVIES JF SHETTY BV FRITZ JE APPELT K BURGESS JA CAMPANALE KM CHIRGADZE NY CLAWSON DK DRESSMAN BA HATCH SD KHALIL DA KOSA MB LUBBEHUSEN PP MUESING MA PATICK AK REICH SH SU KS TATLOCK JH
Citation: Sw. Kaldor et al., VIRACEPT (NELFINAVIR MESYLATE, AG1343) - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE, Journal of medicinal chemistry, 40(24), 1997, pp. 3979-3985
DISCOVERY OF ANTIRHINOVIRAL LEADS BY SCREENING A COMBINATORIAL LIBRARY OF UREAS PREPARED USING COVALENT SCAVENGERS
Authors: KALDOR SW FRITZ JE TANG J MCKINNEY ER
Citation: Sw. Kaldor et al., DISCOVERY OF ANTIRHINOVIRAL LEADS BY SCREENING A COMBINATORIAL LIBRARY OF UREAS PREPARED USING COVALENT SCAVENGERS, Bioorganic & medicinal chemistry letters, 6(24), 1996, pp. 3041-3044
USE OF SOLID SUPPORTED NUCLEOPHILES AND ELECTROPHILES FOR THE PURIFICATION OF NONPEPTIDE SMALL-MOLECULE LIBRARIES
Authors: KALDOR SW SIEGEL MG FRITZ JE DRESSMAN BA HAHN PJ
Citation: Sw. Kaldor et al., USE OF SOLID SUPPORTED NUCLEOPHILES AND ELECTROPHILES FOR THE PURIFICATION OF NONPEPTIDE SMALL-MOLECULE LIBRARIES, Tetrahedron letters, 37(40), 1996, pp. 7193-7196
A SYSTEMATIC STUDY OF P-1-P-3 SPANNING SIDE-CHAINS FOR THE INHIBITIONOF HIV-1 PROTEASE
Authors: KALDOR SW APPELT K FRITZ JE HAMMOND M CROWELL TA BAXTER AJ HATCH SD WISKERCHEN M MUESING MA
Citation: Sw. Kaldor et al., A SYSTEMATIC STUDY OF P-1-P-3 SPANNING SIDE-CHAINS FOR THE INHIBITIONOF HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 715-720
A CONVENIENT, LARGE-SCALE SYNTHESIS OF N-CBZ-(S-PHENYL)-L-CYSTEINE
Authors: MARZONI G KALDOR SW TRIPPE AJ SHAMBLIN BM FRITZ JE
Citation: G. Marzoni et al., A CONVENIENT, LARGE-SCALE SYNTHESIS OF N-CBZ-(S-PHENYL)-L-CYSTEINE, Synthetic communications, 25(16), 1995, pp. 2475-2482
NEW DIPEPTIDE ISOSTERES USEFUL FOR THE INHIBITION OF HIV-1 PROTEASE
Authors: KALDOR SW HAMMOND M DRESSMAN BA FRITZ JE CROWELL TA HERMANN RA
Citation: Sw. Kaldor et al., NEW DIPEPTIDE ISOSTERES USEFUL FOR THE INHIBITION OF HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 4(11), 1994, pp. 1385-1390
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