A NOVEL-APPROACH TO CARBOCYCLIC ANALOGS OF NUCLEOSIDES

[1] TETRAFLUOROBORIC ACID, AN EFFICIENT CATALYST IN CARBOHYDRATE PROTECTION AND DEPROTECTION REACTIONS [J]. CARBOHYDRATE RESEARCH, 1985, 137 (MAR) : 282 - 290

[2] ENANTIOSELECTIVE SYNTHESIS OF THE CARBOCYCLIC NUCLEOSIDES (-)-ARISTEROMYCIN AND (-)-NEPLANOCIN-A BY A CHEMICOENZYMATIC APPROACH [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (12) : 4049 - 4055

[3] COREY EJ, 1979, TETRAHEDRON LETT, P399

[4] SYNTHESIS OF CARBOCYCLIC AMINONUCLEOSIDES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (12) : 2311 - 2320

[5] EICHBERGER G, TETRAHEDRON LETT

[6] SYNTHESIS AND ANTIVIRAL ACTIVITY OF THE CARBOCYCLIC ANALOGS OF (E)-5-(2-HALOVINYL)-2'-DEOXYURIDINES AND (E)-5-(2-HALOVINYL)-2'-DEOXYCYTIDINES [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (05) : 550 - 555

[7] RESOLUTION OF ARISTEROMYCIN ENANTIOMERS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (10) : 1385 - 1386

[8] REGIOSPECIFIC SYNTHESIS OF CYCLOPENTANE ANALOGS OF (2'- AND 3'-DEOXY-THREO-PENTOFURANOSYL)-URACIL AND -2-THIOURACIL NUCLEOSIDES [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1985, 63 (10): : 2787 - 2797

[9] CHIRAL ELECTROPHILIC SYNTHETIC BUILDING-BLOCKS WITH 4 DIFFERENT FUNCTIONAL-GROUPS FROM TARTARIC ACID, 2,3-EPOXY-BUTANEDIOL AND 3,4-EPOXY-BUTANEDIOL DERIVATIVES IN ALL 4 STEREOISOMERIC FORMS [J]. HELVETICA CHIMICA ACTA, 1981, 64 (03) : 687 - 702

[10] (+/-)-2-AMINO-3,4-DIHYDRO-7-[2,3-DIHYDROXY-4-(HYDROXYMETHYL)-1-CYCLOPENTYL]-7H-PYRROLO[2,3-D]PYRIMIDIN-4-ONES - NEW CARBOCYCLIC ANALOGS OF 7-DEAZAGUANOSINE WITH ANTIVIRAL ACTIVITY [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (10) : 1477 - 1480

[1] TETRAFLUOROBORIC ACID, AN EFFICIENT CATALYST IN CARBOHYDRATE PROTECTION AND DEPROTECTION REACTIONS [J]. CARBOHYDRATE RESEARCH, 1985, 137 (MAR) : 282 - 290

[2] ENANTIOSELECTIVE SYNTHESIS OF THE CARBOCYCLIC NUCLEOSIDES (-)-ARISTEROMYCIN AND (-)-NEPLANOCIN-A BY A CHEMICOENZYMATIC APPROACH [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (12) : 4049 - 4055

[3] COREY EJ, 1979, TETRAHEDRON LETT, P399

[4] SYNTHESIS OF CARBOCYCLIC AMINONUCLEOSIDES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (12) : 2311 - 2320

[5] EICHBERGER G, TETRAHEDRON LETT

[6] SYNTHESIS AND ANTIVIRAL ACTIVITY OF THE CARBOCYCLIC ANALOGS OF (E)-5-(2-HALOVINYL)-2'-DEOXYURIDINES AND (E)-5-(2-HALOVINYL)-2'-DEOXYCYTIDINES [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (05) : 550 - 555

[7] RESOLUTION OF ARISTEROMYCIN ENANTIOMERS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (10) : 1385 - 1386

[8] REGIOSPECIFIC SYNTHESIS OF CYCLOPENTANE ANALOGS OF (2'- AND 3'-DEOXY-THREO-PENTOFURANOSYL)-URACIL AND -2-THIOURACIL NUCLEOSIDES [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1985, 63 (10): : 2787 - 2797

[9] CHIRAL ELECTROPHILIC SYNTHETIC BUILDING-BLOCKS WITH 4 DIFFERENT FUNCTIONAL-GROUPS FROM TARTARIC ACID, 2,3-EPOXY-BUTANEDIOL AND 3,4-EPOXY-BUTANEDIOL DERIVATIVES IN ALL 4 STEREOISOMERIC FORMS [J]. HELVETICA CHIMICA ACTA, 1981, 64 (03) : 687 - 702

[10] (+/-)-2-AMINO-3,4-DIHYDRO-7-[2,3-DIHYDROXY-4-(HYDROXYMETHYL)-1-CYCLOPENTYL]-7H-PYRROLO[2,3-D]PYRIMIDIN-4-ONES - NEW CARBOCYCLIC ANALOGS OF 7-DEAZAGUANOSINE WITH ANTIVIRAL ACTIVITY [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1985, 28 (10) : 1477 - 1480