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Results: 1-10 |
Results: 10
PRACTICAL SYNTHESIS OF ANTI-METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS (MRSA) CARBAPENEM L-742,728
Authors: YASUDA N HUFFMAN MA HO GJ XAVIER LC YANG CH EMERSON KM TSAY FR LI YL KRESS MH RIEGER DL KARADY S SOHAR P ABRAMSON NL DECAMP AE MATHRE DJ DOUGLAS AW DOLLING UH GRABOWSKI EJJ REIDER PJ
Citation: N. Yasuda et al., PRACTICAL SYNTHESIS OF ANTI-METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS (MRSA) CARBAPENEM L-742,728, Journal of organic chemistry, 63(16), 1998, pp. 5438-5446
DEVELOPMENT OF ORALLY-ACTIVE OXYTOCIN ANTAGONISTS - STUDIES ON DIN-3-YLMETHYL)PIPERIDIN-4-YLOXY]-2-METHOXYBENZOYL IPERIDIN-4-YL)-1,4-DIHYDROBENZ[D][1,3]OXAZIN-2-ONE (L-372,662) AND RELATED PYRIDINES
Authors: BELL IM ERB JM FREIDINGER RM GALLICCHIO SN GUARE JP GUIDOTTI MT HALPIN RA HOBBS DW HOMNICK CF KUO MS LIS EV MATHRE DJ MICHELSON SR PAWLUCZYK JM PETTIBONE DJ REISS DR VICKERS S WILLIAMS PD WOYDEN CJ
Citation: Im. Bell et al., DEVELOPMENT OF ORALLY-ACTIVE OXYTOCIN ANTAGONISTS - STUDIES ON DIN-3-YLMETHYL)PIPERIDIN-4-YLOXY]-2-METHOXYBENZOYL IPERIDIN-4-YL)-1,4-DIHYDROBENZ[D][1,3]OXAZIN-2-ONE (L-372,662) AND RELATED PYRIDINES, Journal of medicinal chemistry, 41(12), 1998, pp. 2146-2163
HIGH-PERFORMANCE, PURITY-INDICATING LIQUID-CHROMATOGRAPHIC METHOD FORTHE OXYTOCIN ANTAGONIST, L-368,899
Authors: PRABHU SV COOPER SE MATHRE DJ NATISHAN TK ELLISON DK TWAY PC
Citation: Sv. Prabhu et al., HIGH-PERFORMANCE, PURITY-INDICATING LIQUID-CHROMATOGRAPHIC METHOD FORTHE OXYTOCIN ANTAGONIST, L-368,899, Journal of chromatography, 731(1-2), 1996, pp. 331-335
HIGHLY EFFICIENT SYNTHESIS OF FIBRINOGEN RECEPTOR ANTAGONIST L-734,217 VIA A NOVEL CHEMOSELECTIVE SILYL-MEDIATED CONJUGATE ADDITION OF DELTA-LACTAMS TO 4-VINYLPYRIDINE
Authors: CHUNG JYL HUGHES DL ZHAO DL SONG ZG MATHRE DJ HO GJ MCNAMARA JM DOUGLAS AW REAMER RA TSAY FR VARSOLONA R MCCAULEY J GRABOWSKI EJJ REIDER PJ
Citation: Jyl. Chung et al., HIGHLY EFFICIENT SYNTHESIS OF FIBRINOGEN RECEPTOR ANTAGONIST L-734,217 VIA A NOVEL CHEMOSELECTIVE SILYL-MEDIATED CONJUGATE ADDITION OF DELTA-LACTAMS TO 4-VINYLPYRIDINE, Journal of organic chemistry, 61(1), 1996, pp. 215-222
NYL-4-((3-OXO-1,2,4-TRIAZOL-5-YL)METHYL)MORPHOLINE .1. A POTENT, ORALLY-ACTIVE, MORPHOLINE-BASED HUMAN NEUROKININ-1 RECEPTOR ANTAGONIST
Authors: HALE JJ MILLS SG MACCOSS M SHAH SK QI HB MATHRE DJ CASCIERI MA SADOWSKI S STRADER CD MACINTYRE DE METZGER JM
Citation: Jj. Hale et al., NYL-4-((3-OXO-1,2,4-TRIAZOL-5-YL)METHYL)MORPHOLINE .1. A POTENT, ORALLY-ACTIVE, MORPHOLINE-BASED HUMAN NEUROKININ-1 RECEPTOR ANTAGONIST, Journal of medicinal chemistry, 39(9), 1996, pp. 1760-1762
LITHIUM-INITIATED IMIDE FORMATION - A SIMPLE METHOD FOR N-ACYLATION OF 2-OXAZOLIDINONES AND BORNANE-2,10-SULTAM
Authors: HO GJ MATHRE DJ
Citation: Gj. Ho et Dj. Mathre, LITHIUM-INITIATED IMIDE FORMATION - A SIMPLE METHOD FOR N-ACYLATION OF 2-OXAZOLIDINONES AND BORNANE-2,10-SULTAM, Journal of organic chemistry, 60(7), 1995, pp. 2271-2273
CARBODIIMIDE-MEDIATED AMIDE FORMATION IN A 2-PHASE SYSTEM - A HIGH-YIELD AND LOW-RACEMIZATION PROCEDURE FOR PEPTIDE-SYNTHESIS
Authors: HO GJ EMERSON KM MATHRE DJ SHUMAN RF GRABOWSKI EJJ
Citation: Gj. Ho et al., CARBODIIMIDE-MEDIATED AMIDE FORMATION IN A 2-PHASE SYSTEM - A HIGH-YIELD AND LOW-RACEMIZATION PROCEDURE FOR PEPTIDE-SYNTHESIS, Journal of organic chemistry, 60(11), 1995, pp. 3569-3570
DIRECT ISOMERIC SEPARATION OF A 3-HYDROXYPROLINE-CONTAINING PRODRUG, L-693989, BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH A POROUS GRAPHITIC CARBON COLUMN
Authors: BELL C TSAI EW IP DP MATHRE DJ
Citation: C. Bell et al., DIRECT ISOMERIC SEPARATION OF A 3-HYDROXYPROLINE-CONTAINING PRODRUG, L-693989, BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH A POROUS GRAPHITIC CARBON COLUMN, Journal of chromatography, 675(1-2), 1994, pp. 248-252
DIRECT CONVERSION OF ACTIVATED ALCOHOLS TO AZIDES USING DIPHENYL PHOSPHORAZIDATE - A PRACTICAL ALTERNATIVE TO MITSUNOBU CONDITIONS
Authors: THOMPSON AS HUMPHREY GR DEMARCO AM MATHRE DJ GRABOWSKI EJJ
Citation: As. Thompson et al., DIRECT CONVERSION OF ACTIVATED ALCOHOLS TO AZIDES USING DIPHENYL PHOSPHORAZIDATE - A PRACTICAL ALTERNATIVE TO MITSUNOBU CONDITIONS, Journal of organic chemistry, 58(22), 1993, pp. 5886-5888
A PRACTICAL PROCESS FOR THE PREPARATION OF 3-DIPHENYL-1H,3H-PYRROLO[1,2-C]-[1,3,2]OXAZABOROLE BORANE - A HIGHLY ENANTIOSELECTIVE STOICHIOMETRIC AND CATALYTIC REDUCING AGENT
Authors: MATHRE DJ THOMPSON AS DOUGLAS AW HOOGSTEEN K CARROLL JD CORLEY EG GRABOWSKI EJJ
Citation: Dj. Mathre et al., A PRACTICAL PROCESS FOR THE PREPARATION OF 3-DIPHENYL-1H,3H-PYRROLO[1,2-C]-[1,3,2]OXAZABOROLE BORANE - A HIGHLY ENANTIOSELECTIVE STOICHIOMETRIC AND CATALYTIC REDUCING AGENT, Journal of organic chemistry, 58(10), 1993, pp. 2880-2888
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