A facile synthetic method for 2-fluoroindolizines from 1-chloro-2,2,2-trifluoroethane (HCFC-133a) and 1,1,1,2-tetrafluoroethane (HFC-134a)

Journal of Fluorine Chemistry

Volumn 122, Issue 2, 2003, Pages 171-174

  Wu, Kai ^a   Chen, Qing Yun ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

1,1,1,2 Tetrafluoroethane (HFC 134a); 1,3 Dipolar addition; 1 Chloro 2,2,2 trifluoroethane (HCFC 133a); 2 Fluoroindolizine; Cycloimmonium N ylide

Indexed keywords

(2 FLUORO 6 METHYLINDOLIZIN 3 YL)PHENYLMETHANONE; (2 FLUOROPYRROLO[2,1 A]ISOQUINOLIN 3 YL)PHENYLMETHANONE; 2 FLUORO 6 METHYLINDOLIZINE 3 CARBOXYLIC ACID ETHYL ESTER; 2 FLUOROINDOLIZINE 3 CARBOXYLIC ACID ETHYL ESTER; 2 FLUOROINDOLIZINE DERIVATIVE; ALKANE DERIVATIVE; BROMINE DERIVATIVE; DIMETHYL SULFOXIDE; GLASS; INDOLIZINE DERIVATIVE; ISOQUINOLINE DERIVATIVE; NORFLURANE; POTASSIUM HYDROXIDE; PSYCHOTROPIC AGENT; PYRIDINIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ATMOSPHERIC PRESSURE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; CYCLOADDITION; DRUG SYNTHESIS; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLARIZATION; TEMPERATURE;

EID: 0042303907     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-1139(03)00055-1     Document Type: Article

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