USE OF ALLYL GROUP AS A BLOCKING GROUP FOR SYNTHESIS OF N-SUBSTITUTED PURINES

[1] SYNTHESIS OF SOME ALKYLATED ADENINES AS POTENTIAL ANTIMETABOLITES [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1964, 42 (07): : 1599 - &

[2] (2-CHLOROETHYLTHIO)PURINES AND CORRESPONDING DIHYDROTHIAZOLOPURINES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1961, 26 (09) : 3446 - &

[3] THE METHYLATION OF ADENOSINE AND ADENYLIC ACID [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1960, (FEB): : 539 - 545

[4] CUNNINGHAM J, 1964, TETRAHEDRON LETT, P1191

[5] PURINE NUCLEOSIDES .3. METHYLATION STUDIES OF CERTAIN NATURALLY OCCURRING PURINE NUCLEOSIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (02) : 193 - &

[6] SYNTHESIS OF 7-SUBSTITUTED ADENINES THROUGH USE OF A BLOCKING GROUP AT 3-POSITION - SITE OF ALKYLATION OF 7-SUBSTITUTED ADENINES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (22) : 3719 - &

[7] SYNTHESIS OF COMPOUNDS POSSESSING KINETIN ACTIVITY . USE OF BLOCKING GROUP AT 9-POSITION OF ADENINE FOR SYNTHESIS OF 1-SUBSTITUTED ADENINES [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1964, 51 (01) : 73 - &

[8] DIRECTIVE INFLUENCES IN PREPARATION OF PURINE NUCLEOSIDES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1963, 28 (09) : 2304 - &

[9] SYNTHESIS OF ANOMERIC 7-D-RIBOFURANOSYLADENINES AND IDENTIFICATION OF NUCLEOSIDE FROM PSEUDOVITAMIN B12 [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (17) : 2672 - &

[10] MONTGOMERY JA, 1964, J HETEROCYCLIC CHEM, V1, P115

[1] SYNTHESIS OF SOME ALKYLATED ADENINES AS POTENTIAL ANTIMETABOLITES [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1964, 42 (07): : 1599 - &

[2] (2-CHLOROETHYLTHIO)PURINES AND CORRESPONDING DIHYDROTHIAZOLOPURINES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1961, 26 (09) : 3446 - &

[3] THE METHYLATION OF ADENOSINE AND ADENYLIC ACID [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1960, (FEB): : 539 - 545

[4] CUNNINGHAM J, 1964, TETRAHEDRON LETT, P1191

[5] PURINE NUCLEOSIDES .3. METHYLATION STUDIES OF CERTAIN NATURALLY OCCURRING PURINE NUCLEOSIDES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (02) : 193 - &

[6] SYNTHESIS OF 7-SUBSTITUTED ADENINES THROUGH USE OF A BLOCKING GROUP AT 3-POSITION - SITE OF ALKYLATION OF 7-SUBSTITUTED ADENINES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (22) : 3719 - &

[7] SYNTHESIS OF COMPOUNDS POSSESSING KINETIN ACTIVITY . USE OF BLOCKING GROUP AT 9-POSITION OF ADENINE FOR SYNTHESIS OF 1-SUBSTITUTED ADENINES [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1964, 51 (01) : 73 - &

[8] DIRECTIVE INFLUENCES IN PREPARATION OF PURINE NUCLEOSIDES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1963, 28 (09) : 2304 - &

[9] SYNTHESIS OF ANOMERIC 7-D-RIBOFURANOSYLADENINES AND IDENTIFICATION OF NUCLEOSIDE FROM PSEUDOVITAMIN B12 [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (17) : 2672 - &

[10] MONTGOMERY JA, 1964, J HETEROCYCLIC CHEM, V1, P115