RING OPEN ANALOGS OF DEOXYNUCLEOTIDES

[1] BUTHALA DA, 1964, P SOC EXP BIOL MED, V115, P69, DOI 10.3181/00379727-115-28834

[2] ANTI-VIRAL ACTIVITY OF ALIPHATIC NUCLEOSIDE ANALOGS - STRUCTURE-FUNCTION RELATIONSHIP [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (05) : 510 - 513

[3] DECLERCQ E, 1978, J CARB-NUCLEOS-NUCL, V5, P187

[4] TOXICITY OF 9-BETA-D-ARABINOFURANOSYLADENINE TO PURINE-REQUIRING ESCHERICHIA COLI [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1962, 59 (02) : 468 - +

[5] SYNTHESIS OF THYMIDINE OLIGONUCLEOTIDES BY PHOSPHITE TRIESTER INTERMEDIATES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (12) : 3655 - 3661

[6] OLIGONUCLEOTIDIC COMPOUNDS .55. SYNTHESIS OF MODIFIED TERMINATOR (UGA) AND INITIATOR (AUG) CODONS CONTAINING SOME HYDROXYALKYL ANALOGUES OF NUCLEOSIDES [J]. COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1975, 40 (08) : 2353 - 2363

[7] TERT-BUTYLDIMETHYLSILYL GROUP AS A PROTECTING GROUP IN DEOXYNUCLEOSIDES [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1973, 51 (22): : 3799 - 3807

[8] SYNTHESIS OF OLIGORIBONUCLEOTIDES .2. USE OF SILYL PROTECTING GROUPS IN NUCLEOSIDE AND NUCLEOTIDE CHEMISTRY .7. [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1978, 56 (21): : 2768 - 2780

[9] NOVEL SUBSTRATE OF ADENOSINE DEAMINASE [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1971, 45 (02) : 297 - &

[10] PANDIT U K, 1972, Synthetic Communications, V2, P345, DOI 10.1080/00397917208081778

[1] BUTHALA DA, 1964, P SOC EXP BIOL MED, V115, P69, DOI 10.3181/00379727-115-28834

[2] ANTI-VIRAL ACTIVITY OF ALIPHATIC NUCLEOSIDE ANALOGS - STRUCTURE-FUNCTION RELATIONSHIP [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (05) : 510 - 513

[3] DECLERCQ E, 1978, J CARB-NUCLEOS-NUCL, V5, P187

[4] TOXICITY OF 9-BETA-D-ARABINOFURANOSYLADENINE TO PURINE-REQUIRING ESCHERICHIA COLI [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1962, 59 (02) : 468 - +

[5] SYNTHESIS OF THYMIDINE OLIGONUCLEOTIDES BY PHOSPHITE TRIESTER INTERMEDIATES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (12) : 3655 - 3661

[6] OLIGONUCLEOTIDIC COMPOUNDS .55. SYNTHESIS OF MODIFIED TERMINATOR (UGA) AND INITIATOR (AUG) CODONS CONTAINING SOME HYDROXYALKYL ANALOGUES OF NUCLEOSIDES [J]. COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1975, 40 (08) : 2353 - 2363

[7] TERT-BUTYLDIMETHYLSILYL GROUP AS A PROTECTING GROUP IN DEOXYNUCLEOSIDES [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1973, 51 (22): : 3799 - 3807

[8] SYNTHESIS OF OLIGORIBONUCLEOTIDES .2. USE OF SILYL PROTECTING GROUPS IN NUCLEOSIDE AND NUCLEOTIDE CHEMISTRY .7. [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1978, 56 (21): : 2768 - 2780

[9] NOVEL SUBSTRATE OF ADENOSINE DEAMINASE [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1971, 45 (02) : 297 - &

[10] PANDIT U K, 1972, Synthetic Communications, V2, P345, DOI 10.1080/00397917208081778