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Results: 1-25 | 26-50 | 51-53
Results: 26-50/53
REMOVAL OF ACETAL, SILYL, AND 4,4'-DIMETHOXYTRITYL PROTECTING GROUPS FROM HYDROXYL FUNCTIONS OF CARBOHYDRATES AND NUCLEOSIDES WITH CLAY IN AQUEOUS-METHANOL
Authors: ASAKURA J ROBINS MJ ASAKA Y KIM TH
Citation: J. Asakura et al., REMOVAL OF ACETAL, SILYL, AND 4,4'-DIMETHOXYTRITYL PROTECTING GROUPS FROM HYDROXYL FUNCTIONS OF CARBOHYDRATES AND NUCLEOSIDES WITH CLAY IN AQUEOUS-METHANOL, Journal of organic chemistry, 61(25), 1996, pp. 9026-9027
EFFICIENT DEHOMOLOGATION OF DI-O-ISOPROPYLIDENEHEXOFURANOSE DERIVATIVES TO GIVE O-ISOPROPYLIDENEPENTOFURANOSES BY SEQUENTIAL TREATMENT WITHPERIODIC ACID IN ETHYL-ACETATE AND SODIUM-BOROHYDRIDE
Authors: XIE MQ BERGES DA ROBINS MJ
Citation: Mq. Xie et al., EFFICIENT DEHOMOLOGATION OF DI-O-ISOPROPYLIDENEHEXOFURANOSE DERIVATIVES TO GIVE O-ISOPROPYLIDENEPENTOFURANOSES BY SEQUENTIAL TREATMENT WITHPERIODIC ACID IN ETHYL-ACETATE AND SODIUM-BOROHYDRIDE, Journal of organic chemistry, 61(15), 1996, pp. 5178-5179
INACTIVATION OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE BY AMIDE AND ESTER DERIVATIVES OF ADENOSINE-5'-CARBOXYLIC ACID
Authors: WNUK SF LIU SM YUAN CS BORCHARDT RT ROBINS MJ
Citation: Sf. Wnuk et al., INACTIVATION OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE BY AMIDE AND ESTER DERIVATIVES OF ADENOSINE-5'-CARBOXYLIC ACID, Journal of medicinal chemistry, 39(21), 1996, pp. 4162-4166
MECHANISM-BASED INHIBITION OF RIBONUCLEOTIDE REDUCTASES
Authors: SILVA DJ VANDERDONK W LAWRENCE C GERFEN G LICHT S SAMANO V ROBINS MJ STUBBE J
Citation: Dj. Silva et al., MECHANISM-BASED INHIBITION OF RIBONUCLEOTIDE REDUCTASES, Biochemistry, 35(28), 1996, pp. 87-87
NUCLEIC-ACID RELATED-COMPOUNDS .91. BIOMIMETIC REACTIONS ARE IN HARMONY WITH LOSS OF 2'-SUBSTITUENTS AS FREE-RADICALS (NOT ANIONS) DURING MECHANISM-BASED INACTIVATION OF RIBONUCLEOTIDE REDUCTASES - DIFFERENTIAL INTERACTIONS OF AZIDE, HALOGEN, AND ALKYLTHIO GROUPS WITH TRIBUTYLSTANNANE AND TRIPHENYLSILANE
Authors: ROBINS MJ WNUK SF HERNANDEZTHIRRING AE SAMANO MC
Citation: Mj. Robins et al., NUCLEIC-ACID RELATED-COMPOUNDS .91. BIOMIMETIC REACTIONS ARE IN HARMONY WITH LOSS OF 2'-SUBSTITUENTS AS FREE-RADICALS (NOT ANIONS) DURING MECHANISM-BASED INACTIVATION OF RIBONUCLEOTIDE REDUCTASES - DIFFERENTIAL INTERACTIONS OF AZIDE, HALOGEN, AND ALKYLTHIO GROUPS WITH TRIBUTYLSTANNANE AND TRIPHENYLSILANE, Journal of the American Chemical Society, 118(46), 1996, pp. 11341-11348
BIOMIMETIC MODELING OF THE DECOMPOSITION OF 2'-CHLORO-2'-DEOXYNUCLEOTIDES BY RIBONUCLEOTIDE REDUCTASES TO GIVE 3(2H)-FURANONES WHICH CAN EFFECT MECHANISM-BASED INACTIVATION BY MICHAEL-TYPE ALKYLATION
Authors: ROBINS MJ GUO ZQ SAMANO MC WNUK SF
Citation: Mj. Robins et al., BIOMIMETIC MODELING OF THE DECOMPOSITION OF 2'-CHLORO-2'-DEOXYNUCLEOTIDES BY RIBONUCLEOTIDE REDUCTASES TO GIVE 3(2H)-FURANONES WHICH CAN EFFECT MECHANISM-BASED INACTIVATION BY MICHAEL-TYPE ALKYLATION, Journal of the American Chemical Society, 118(45), 1996, pp. 11317-11318
STANNYL RADICAL-MEDIATED CLEAVAGE OF PI-DEFICIENT HETEROCYCLIC SULFONES - SYNTHESIS OF ALPHA-FLUORO ESTERS AND THE FIRST HOMONUCLEOSIDE ALPHA-FLUOROMETHYLENE PHOSPHONATE
Authors: WNUK SF ROBINS MJ
Citation: Sf. Wnuk et Mj. Robins, STANNYL RADICAL-MEDIATED CLEAVAGE OF PI-DEFICIENT HETEROCYCLIC SULFONES - SYNTHESIS OF ALPHA-FLUORO ESTERS AND THE FIRST HOMONUCLEOSIDE ALPHA-FLUOROMETHYLENE PHOSPHONATE, Journal of the American Chemical Society, 118(10), 1996, pp. 2519-2520
RATIONAL APPROACHES TO THE DESIGN OF MECHANISM-BASED INHIBITORS OF S-ADENOSYLHOMOCYSTEINE HYDROLASE
Authors: YUAN CS LIU SM WNUK SF ROBINS MJ BORCHARDT RT
Citation: Cs. Yuan et al., RATIONAL APPROACHES TO THE DESIGN OF MECHANISM-BASED INHIBITORS OF S-ADENOSYLHOMOCYSTEINE HYDROLASE, Nucleosides & nucleotides, 14(3-5), 1995, pp. 439-447
RIBONUCLEOTIDE REDUCTASE TARGETS FOR CHEMOTHERAPY - MECHANISTIC ASPECTS AND BIOLOGICALLY-ACTIVE AGENTS
Authors: ROBINS MJ SAMANO MC SAMANO V
Citation: Mj. Robins et al., RIBONUCLEOTIDE REDUCTASE TARGETS FOR CHEMOTHERAPY - MECHANISTIC ASPECTS AND BIOLOGICALLY-ACTIVE AGENTS, Nucleosides & nucleotides, 14(3-5), 1995, pp. 485-493
NUCLEIC-ACID RELATED-COMPOUNDS .88. EFFICIENT CONVERSIONS OF RIBONUCLEOSIDES INTO THEIR 2',3'-ANHYDRO, 2'(AND 3')-DEOXY, 2',3'-DIDEHYDRO-2',3'-DIDEOXY, AND 2',3'-DIDEOXYNUCLEOSIDE ANALOGS
Authors: ROBINS MJ WILSON JS MADEJ D LOW NH HANSSKE F WNUK SF
Citation: Mj. Robins et al., NUCLEIC-ACID RELATED-COMPOUNDS .88. EFFICIENT CONVERSIONS OF RIBONUCLEOSIDES INTO THEIR 2',3'-ANHYDRO, 2'(AND 3')-DEOXY, 2',3'-DIDEHYDRO-2',3'-DIDEOXY, AND 2',3'-DIDEOXYNUCLEOSIDE ANALOGS, Journal of organic chemistry, 60(24), 1995, pp. 7902-7908
NUCLEIC-ACID RELATED-COMPOUNDS .87. NUCLEOPHILIC FUNCTIONALIZATION OFCYTIDINE AND 2'-DEOXYCYTIDINE DERIVATIVES VIA ELABORATION OF THE 4-AMINO GROUP INTO A READILY DISPLACED 1,2,4-TRIAZOL-4-YL SUBSTITUENT
Authors: MILES RW SAMANO V ROBINS MJ
Citation: Rw. Miles et al., NUCLEIC-ACID RELATED-COMPOUNDS .87. NUCLEOPHILIC FUNCTIONALIZATION OFCYTIDINE AND 2'-DEOXYCYTIDINE DERIVATIVES VIA ELABORATION OF THE 4-AMINO GROUP INTO A READILY DISPLACED 1,2,4-TRIAZOL-4-YL SUBSTITUENT, Journal of organic chemistry, 60(21), 1995, pp. 7066-7069
NUCLEIC-ACID RELATED-COMPOUNDS .86. NUCLEOPHILIC FUNCTIONALIZATION OFADENINE, ADENOSINE, TUBERCIDIN, AND FORMYCIN DERIVATIVES VIA ELABORATION OF THE HETEROCYCLIC AMINO GROUP INTO A READILY DISPLACED 1,2,4-TRIAZOL-4-YL SUBSTITUENT
Authors: MILES RW SAMANO V ROBINS MJ
Citation: Rw. Miles et al., NUCLEIC-ACID RELATED-COMPOUNDS .86. NUCLEOPHILIC FUNCTIONALIZATION OFADENINE, ADENOSINE, TUBERCIDIN, AND FORMYCIN DERIVATIVES VIA ELABORATION OF THE HETEROCYCLIC AMINO GROUP INTO A READILY DISPLACED 1,2,4-TRIAZOL-4-YL SUBSTITUENT, Journal of the American Chemical Society, 117(22), 1995, pp. 5951-5957
SELECTED ASPECTS OF THE CHEMISTRY AND BIOCHEMISTRY OF SULFUR-CONTAINING NUCLEOSIDES
Authors: ROBINS MJ WNUK SF
Citation: Mj. Robins et Sf. Wnuk, SELECTED ASPECTS OF THE CHEMISTRY AND BIOCHEMISTRY OF SULFUR-CONTAINING NUCLEOSIDES, Phosphorus, sulfur and silicon and the related elements, 95-6(1-4), 1994, pp. 71-88
)-5',6'-DIDEHYDRO-6'-DEOXY-6'-FLUORO-HOMOADENOSINE (EDDFHA) - A SUBSTRATE THAT MEASURES THE HYDROLYTIC ACTIVITY OF S-ADENOSYL-L-HOMOCYSTEINE (ADOHCY) HYDROLASE
Authors: YUAN CS WNUK SF LIU S ROBINS MJ BORCHARDT RT
Citation: Cs. Yuan et al., )-5',6'-DIDEHYDRO-6'-DEOXY-6'-FLUORO-HOMOADENOSINE (EDDFHA) - A SUBSTRATE THAT MEASURES THE HYDROLYTIC ACTIVITY OF S-ADENOSYL-L-HOMOCYSTEINE (ADOHCY) HYDROLASE, The FASEB journal, 8(7), 1994, pp. 10001412-10001412
SYNTHESIS OF SUBSTITUTED-BENZYL AND SUGAR-MODIFIED ANALOGS OF 6-N-(4-NITROBENZYL)ADENOSINE AND THEIR INTERACTIONS WITH ES NUCLEOSIDE TRANSPORT-SYSTEMS
Authors: ROBINS MJ ASAKURA J KANEKO M SHIBUYA S JAKOBS ES AGBANYO FR CASS CE PATERSON ARP
Citation: Mj. Robins et al., SYNTHESIS OF SUBSTITUTED-BENZYL AND SUGAR-MODIFIED ANALOGS OF 6-N-(4-NITROBENZYL)ADENOSINE AND THEIR INTERACTIONS WITH ES NUCLEOSIDE TRANSPORT-SYSTEMS, Nucleosides & nucleotides, 13(6-7), 1994, pp. 1627-1646
NUCLEIC-ACID RELATED-COMPOUNDS .82. CONVERSIONS OF ADENOSINE TO INOSINE 5-BETA-THIOETHER DERIVATIVES WITH ASPERGILLUS-ORYZAE ADENOSINE-DEAMINASE OR ALKYL NITRATES - SUBSTRATE AND INHIBITORY ACTIVITIES OF INOSINE 5'-THIOETHER DERIVATIVES WITH PURINE NUCLEOSIDE PHOSPHORYLASE
Authors: WNUK SF STOECKLER JD ROBINS MJ
Citation: Sf. Wnuk et al., NUCLEIC-ACID RELATED-COMPOUNDS .82. CONVERSIONS OF ADENOSINE TO INOSINE 5-BETA-THIOETHER DERIVATIVES WITH ASPERGILLUS-ORYZAE ADENOSINE-DEAMINASE OR ALKYL NITRATES - SUBSTRATE AND INHIBITORY ACTIVITIES OF INOSINE 5'-THIOETHER DERIVATIVES WITH PURINE NUCLEOSIDE PHOSPHORYLASE, Nucleosides & nucleotides, 13(1-3), 1994, pp. 389-403
CONJUGATES OF FLUORESCEIN AND SAENTA -AMINOETHYL)-N-6-(4-NITROBENZYL)-5'-THIOADENOSINE) - FLOW-CYTOMETRY PROBES FOR THE ES NUCLEOSIDE TRANSPORTER ELEMENTS OF THE PLASMA-MEMBRANE
Authors: BUOLAMWINI JK CRAIK JD WILEY JS ROBINS MJ GATI WP CASS CE PATERSON ARP
Citation: Jk. Buolamwini et al., CONJUGATES OF FLUORESCEIN AND SAENTA -AMINOETHYL)-N-6-(4-NITROBENZYL)-5'-THIOADENOSINE) - FLOW-CYTOMETRY PROBES FOR THE ES NUCLEOSIDE TRANSPORTER ELEMENTS OF THE PLASMA-MEMBRANE, Nucleosides & nucleotides, 13(1-3), 1994, pp. 737-751
SYNTHESIS OF 3'-DEOXYADENOSINE-3'-SPIROCYCLOPROPANE, 3'-DEOXYURIDINE-5'-SPIROCYCLOPROPANE, AND 5'-DEOXY-4',5'-METHANOADENOSINE
Authors: SAMANO V ROBINS MJ
Citation: V. Samano et Mj. Robins, SYNTHESIS OF 3'-DEOXYADENOSINE-3'-SPIROCYCLOPROPANE, 3'-DEOXYURIDINE-5'-SPIROCYCLOPROPANE, AND 5'-DEOXY-4',5'-METHANOADENOSINE, Tetrahedron letters, 35(21), 1994, pp. 3445-3448
NUCLEIC-ACID RELATED-COMPOUNDS .80. SYNTHESIS OF 5'-S-(ALKYL AND ARYL)-5'-FLUORO-5'-THIOADENOSINES WITH XENON DIFLUORIDE OR (DIETHYLAMIDO)SULFUR TRIFLUORIDE, HYDROLYSIS IN AQUEOUS BUFFER, AND INHIBITION OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE BY DERIVED ADENOSINE 5'-ALDEHYDE SPECIES
Authors: ROBINS MJ WNUK SF MULLAH KB DALLEY NK YUAN CS LEE YH BORCHARDT RT
Citation: Mj. Robins et al., NUCLEIC-ACID RELATED-COMPOUNDS .80. SYNTHESIS OF 5'-S-(ALKYL AND ARYL)-5'-FLUORO-5'-THIOADENOSINES WITH XENON DIFLUORIDE OR (DIETHYLAMIDO)SULFUR TRIFLUORIDE, HYDROLYSIS IN AQUEOUS BUFFER, AND INHIBITION OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE BY DERIVED ADENOSINE 5'-ALDEHYDE SPECIES, Journal of organic chemistry, 59(3), 1994, pp. 544-555
NUCLEIC-ACID RELATED-COMPOUNDS .84. SYNTHESIS OF 6'-(E AND Z)-HALOHOMOVINYL DERIVATIVES OF ADENOSINE, INACTIVATION OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE, AND CORRELATION OF ANTICANCER AND ANTIVIRAL POTENCIES WITH ENZYME-INHIBITION
Authors: WNUK SF YUAN CS BORCHARDT RT BALZARINI J DECLERCQ E ROBINS MJ
Citation: Sf. Wnuk et al., NUCLEIC-ACID RELATED-COMPOUNDS .84. SYNTHESIS OF 6'-(E AND Z)-HALOHOMOVINYL DERIVATIVES OF ADENOSINE, INACTIVATION OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE, AND CORRELATION OF ANTICANCER AND ANTIVIRAL POTENCIES WITH ENZYME-INHIBITION, Journal of medicinal chemistry, 37(21), 1994, pp. 3579-3587
E)-5',6'-DIDEHYDRO-6'-DEOXY-6'-FLUOROHOMOADENOSINE - A SUBSTRATE THATMEASURES THE HYDROLYTIC ACTIVITY OF S-ADENOSYLHOMOCYSTEINE HYDROLASE
Authors: YUAN CS WNUK SF LIU SM ROBINS MJ BORCHARDT RT
Citation: Cs. Yuan et al., E)-5',6'-DIDEHYDRO-6'-DEOXY-6'-FLUOROHOMOADENOSINE - A SUBSTRATE THATMEASURES THE HYDROLYTIC ACTIVITY OF S-ADENOSYLHOMOCYSTEINE HYDROLASE, Biochemistry, 33(40), 1994, pp. 12305-12311
MECHANISM OF INACTIVATION OF S-ADENOSYLHOMOCYSTEINE HYDROLASE BY (E)-5',6'-DIDEHYDRO-6'-DEOXY-6'-HALOHOMOADENOSINES
Authors: YUAN CS LIU SM WNUK SF ROBINS MJ BORCHARDT RT
Citation: Cs. Yuan et al., MECHANISM OF INACTIVATION OF S-ADENOSYLHOMOCYSTEINE HYDROLASE BY (E)-5',6'-DIDEHYDRO-6'-DEOXY-6'-HALOHOMOADENOSINES, Biochemistry, 33(12), 1994, pp. 3758-3765
2'-DEOXY-2'-METHYLENE DERIVATIVES OF ADENOSINE, GUANOSINE, TUBERCIDIN, CYTIDINE AND URIDINE AS INHIBITORS OF L1210 CELL-GROWTH IN CULTURE
Authors: CORY AH SAMANO V ROBINS MJ CORY JG
Citation: Ah. Cory et al., 2'-DEOXY-2'-METHYLENE DERIVATIVES OF ADENOSINE, GUANOSINE, TUBERCIDIN, CYTIDINE AND URIDINE AS INHIBITORS OF L1210 CELL-GROWTH IN CULTURE, Biochemical pharmacology, 47(2), 1994, pp. 365-371
EFFICIENT CONVERSION OF 6-AMINOPURINES AND NUCLEOSIDES INTO 6-SUBSTITUTED ANALOGS VIA NOVEL 6-(1,2,4-TRIAZOL-4-YL)PURINE DERIVATIVES
Authors: SAMANO V MILES RW ROBINS MJ
Citation: V. Samano et al., EFFICIENT CONVERSION OF 6-AMINOPURINES AND NUCLEOSIDES INTO 6-SUBSTITUTED ANALOGS VIA NOVEL 6-(1,2,4-TRIAZOL-4-YL)PURINE DERIVATIVES, Journal of the American Chemical Society, 116(20), 1994, pp. 9331-9332
FACILE ACCESS TO 2'-O-ACYL PRODRUGS OF BETA-D-ARABINOFURANOSYL)-5(E)-(2-BROMOVINYL)URACIL (BVARAU) VIA REGIOSELECTIVE ESTERASE-CATALYZED HYDROLYSIS OF 2',3',5'-TRIESTERS
Authors: BARALDI PG BAZZANINI R MANFREDINI S SIMONI D ROBINS MJ
Citation: Pg. Baraldi et al., FACILE ACCESS TO 2'-O-ACYL PRODRUGS OF BETA-D-ARABINOFURANOSYL)-5(E)-(2-BROMOVINYL)URACIL (BVARAU) VIA REGIOSELECTIVE ESTERASE-CATALYZED HYDROLYSIS OF 2',3',5'-TRIESTERS, Tetrahedron letters, 34(19), 1993, pp. 3177-3180
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