Synthetic approach to alkoxy-β-(trifluoromethyl)styrenes and their application in the synthesis of new trifluoromethylated heterocycles

Synthesis

Volumn , Issue 13, 2009, Pages 2249-2259

  Muzalevskiy, Vasiliy M ^a   Nenajdenko, Valentine G ^a   Shastin, Aleksey V ^b   Balenkova, Elizabeth S ^a   Haufe, Günter ^c  

^a MOSCOW STATE UNIVERSITY   (Russian Federation)

^b INSTITUTE OF PROBLEMS OF CHEMICAL PHYSICS   (Russian Federation)

^c UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

Alkenes; Alkynes; Ethers; Fluorine; Heterocycles; Nucleophilic substitution

Indexed keywords

ALKENES; ALKYNES; AMINOTHIAZOLE; HETEROCYCLES; HETEROCYCLIC COMPOUND; HIGH YIELD; IMIDAZOPYRIDINE; METHOXY; NUCLEOPHILIC SUBSTITUTION; POTASSIUM TERT-BUTOXIDE; SODIUM METHOXIDE; STARTING MATERIALS; STEREO-SELECTIVE; SYNTHETIC APPROACH; TRIFLUOROMETHYL; TRIFLUOROMETHYL GROUP; TRIFLUOROMETHYLKETONE;

ACETYLENE; COMPLEXATION; ETHERS; FLUORINE; KETONES; OLEFINS; POTASSIUM; SODIUM; SYNTHESIS (CHEMICAL);

STYRENE;

BENZIMIDAZOLE DERIVATIVE; FLUORINE DERIVATIVE; IMIDAZOPYRIDINE DERIVATIVE; KETONE DERIVATIVE; POTASSIUM DERIVATIVE; PYRIMIDINE DERIVATIVE; SODIUM DERIVATIVE; STYRENE DERIVATIVE; THIAZOLE; THIAZOLE DERIVATIVE;

ARTICLE; BROMINATION; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL REACTION; CONTROLLED STUDY; METHYLATION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 67650533749     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1216697     Document Type: Article

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