An efficient synthesis of highly optically active 4-substituted-2(5H)- furanones from chiral 3-bromo-2(5H)-furanone

Chinese Journal of Chemistry

Volumn 22, Issue 11, 2004, Pages 1359-1365

  Fan, Xue E ^a   Huang, Min ^b,c   Huang, Hui ^b,d   Chen, Qing Hua ^a,b  

^a LUOYANG NORMAL COLLEGE   (China)

^b BEIJING NORMAL UNIVERSITY   (China)

^c MAOMING UNIVERSITY   (China)

^d TONGHUA TEACHERS COLLEGE   (China)

Author keywords

Optically active 4 substituted 2(5H) furanone; Pyrimidine or purine base group; Tandem asymmetric Michael addition elimination reaction; X ray crystallography

Indexed keywords

3 BROMO 2(5H) FURANONE; 5 MENTHYLOXY 4 (1' IMIDAZOLYL) 2(5H) FURANONE; 5 MENTHYLOXY 4 (2' NAPHTHOXY) 2(5H) FURANONE; 5 MENTHYLOXY 4 (4' METHYL 2' THIAZOLYLAMINO) 2(5H) FURANONE; 5 MENTHYLOXY 4 (4',6' DIMETHYL 2' PYRIMIDINETHIO) 2(5H) FURANONE; 5 MENTHYLOXY 4 (8' QUINOLINOXY) 2(5H) FURANONE; 5 MENTHYLOXY 4 (9' ADENINYL) 2(5H) FURANONE; 5 MENTHYLOXY 4 MORPHOLINYL 2(5H) FURANONE; 5 MENTHYLOXY 4 PIPERIDINYL 2(5H) FURANONE; 5 MENTHYLOXY 4 PYRROLIDINYL 2(5H) FURANONE; 5 MENTHYLOXY 4 [9' (8' AZAGUANINYL)] 2(5H) FURANONE; FURANONE DERIVATIVE; PURINE DERIVATIVE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHIRALITY; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; MICHAEL ADDITION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; ULTRAVIOLET SPECTROSCOPY; X RAY CRYSTALLOGRAPHY;

EID: 10844221531     PISSN: 1001604X     EISSN: None     Source Type: Journal    
DOI: 10.1002/cjoc.20040221129     Document Type: Article

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