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Volumn , Issue 17, 2004, Pages 2855-2862
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A convenient synthesis of new purinyl-homo-carbonucleosides on a cyclopentane ring fused with pyridazine
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Author keywords
Acylation; Carbocyclic nucleosides; Diols; Heterocycles; Ozonolysis; Pyridazine
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Indexed keywords
OZONE LAYER;
REDUCTION;
SUBSTITUTION REACTIONS;
SYNTHESIS (CHEMICAL);
MESYLATION;
MONOPROTECTION;
PURINE POSITION;
REDUCTIVE CLEAVAGE;
ETHERS;
1,4 DIPHENYL 5,8 DIHYDRO 5,8 METHANOPHTHALAZINE;
5 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 7 [(6 CHLORO 9H PURIN 9 YL)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZINE;
6 CHLOROPURINE;
9 [[7 (HYDROXYMETHYL) 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHYL] 1,9 DIHYDROPURIN 6 ONE;
9 [[7 [(TERT BUTYLDIMETHYLSILYLOXY)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHYL] N CYCLOPENTYL 9H PURIN 6 AMINE;
[7 [(6 CHLORO 9H PURIN 9 YL)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHANOL;
[7 [(6 CYCLOPENTYLAMINO 9H PURIN 9 YL)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHANOL;
[7 [(6 CYCLOPROPYLAMINE 9H PURIN 9 YL)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHYL ACETATE;
[7 [(6 CYCLOPROPYLAMINO 9H PURIN 9 YL)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHANOL;
[7 [(6 METHOXY 9H PURIN 9 YL)METHYL] 1,4 DIPHENYL 6,7 DIHYDRO 5H CYCLOPENTA[D]PYRIDAZIN 5 YL]METHANOL;
CARBOCYCLIC NUCLEOSIDE;
CHLORINE;
CYCLOPENTANE;
HETEROCYCLIC COMPOUND;
PHTHALAZINE DERIVATIVE;
PURINE;
PURINYL HOMO CARBONUCLEOSIDE;
PYRIDAZINE;
PYRIDAZINE DERIVATIVE;
UNCLASSIFIED DRUG;
ACYLATION;
ARTICLE;
CHEMICAL REACTION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
NONHUMAN;
OZONOLYSIS;
STRUCTURE ANALYSIS;
SUBSTITUTION REACTION;
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EID: 10644239990
PISSN: 00397881
EISSN: None
Source Type: Journal
DOI: 10.1055/s-2004-834870 Document Type: Article |
Times cited : (14)
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References (25)
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