Covalent analogues of DNA base-pairs and triplets VII.+ synthesis and cytostatic activity of bis(purin-6-yl)acetylene and -diacetylene nucleosides

Collection of Czechoslovak Chemical Communications

Volumn 69, Issue 10, 2004, Pages 1955-1970

  Nauš, Petr ^a   Votruba, Ivan ^a   Hocek, Michal ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

Author keywords

Alkynes; Base pairs; Cross coupling reactions; Cytostatics; Desilylation; Nucleobases; Nucleosides; Oxidative dimerization; Protecting groups; Purines

Indexed keywords

1 (PURIN 6 YL) 2 [9 (2,3,5 TRI O ACETYL BETA DEXTRO RIBOFURANOSYL)PURIN 6 YL]ETHYNE; 1 [9 (TETRAHYDROPYRAN 2 YL) PURIN 6 YL] 2 [(2,3,5 TRI O ACETYL BETA DEXTRO RIBOFURANOSYL)PURIN 6 YL]ETHYNE; 1,4 BIS[9 (2,3,5 TRI O ACETYL BETA DEXTRO RIBOFURANOSYL)PURIN 6 YL]BUTADIYNE; 1,4 BIS[9 (BETA DEXTRO RIBOFURANOSYL)PURIN 6 YL]BUTADIYNE; 1,4 BIS[9 [2 DEOXY 3,5 BIS O (4 METHYLBENZOYL) BETA DEXTRO ERYTHRO PENTOFURANOSYL]PURIN 6 YL]BUTADIYNE; 9 (2,3,5 TRI O ACETYL BETA DEXTRO RIBOFURANOSYL) 6 [(TRIMETHYLSILYL) ETHYNYL]PURINE; 9 (2,3,5 TRI O ACETYL BETA DEXTRO RIBOFURANOSYL) 6 ETHYNYLPURINE; 9 [2 DEOXY 3,5 BIS O (4 METHYLBENZOYL) BETA DEXTRO ERYTHRO PENTOFURANOSYL] 6 [(TRIMETHYLSILYL)ETHYNYL]PURINE; 9 [2 DEOXY 3,5 BIS O (4 METHYLBENZOYL) BETA DEXTRO ERYTHRO PENTOFURANOSYL] 6 ETHYNYLPURINE; ANTINEOPLASTIC AGENT; BIS(PURIN 6 YL)ETHYNE; BIS[9 (2 DEOXY BETA DEXTRO ERYTHRO PENTOFURANOSYL)PURIN 6 YL]ETHYNE; BIS[9 (2,3,5 TRI O ACETYL BETA DEXTRO RIBOFURANOSYL)PURIN 6 YL]ETHYNE; BIS[9 (BETA DEXTRO RIBOFURANOSYL)PURIN 6 YL]ETHYNE; BIS[9 (TETRAHYDROPYRAN 2 YL)PURIN 6 YL]ETHYNE; BIS[9 [2 DEOXY 3,5 BIS O (4 METHYLBENZOYL) BETA DEXTRO ERYTHRO PENTOFURANOSYL]PURIN 6 YL]ETHYNE; FURAN DERIVATIVE; PURINE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; CYTOSTASIS; DEPROTECTION REACTION; DESILYLATION; DIMERIZATION; DNA REPAIR; DRUG SYNTHESIS; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; SONOGASHIRA REACTION;

EID: 10344240898     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20041955     Document Type: Article

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