A solid-phase approach to novel purine and nucleoside analogs

Bioorganic and Medicinal Chemistry

Volumn 13, Issue 15, 2005, Pages 4760-4766

  Chang, Junbiao ^a,b   Dong, Chunhong ^b   Guo, Xiaohe ^b   Hu, Weidong ^a   Cheng, Senxiang ^a   Wang, Qiang ^a   Chen, Rongfeng ^a  

^a Henan Key Laboratory of Fine Chemicals   (China)

^b UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA   (China)

Author keywords

Condensation; D,L Ribofuranoside; Nucleoside; Purine bases; Solid phase synthesis

Indexed keywords

9 (BETA RIBOFURANOSYL) 2 CHLORO 6 [1 (4 PIPERONYL)PIPERAZINE]PURINE; 9 (BETA RIBOFURANOSYL) 2 PIPERAZINE 6 [1 (4 PIPERONYL)PIPERAZINE]PURINE; NUCLEOSIDE DERIVATIVE; PURINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DRUG SYNTHESIS; NONHUMAN; OXIDATION; REDUCTION; SOLID;

ANTI-HIV AGENTS; MOLECULAR STRUCTURE; NUCLEOSIDES; PURINES; STRUCTURE-ACTIVITY RELATIONSHIP;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 20544464146     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2005.05.007     Document Type: Article

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