A dehydrohalogenation methodology for synthesizing terminal olefins under mild conditions

Synthesis

Volumn , Issue 18, 2006, Pages 3085-3091

  Bérubé, Marie ^a   Kamal, Fatima ^a   Roy, Jenny ^a   Poirier, Donald ^a  

^a UNIVERSITÉ LAVAL   (Canada)

Author keywords

Alkenes; Alkyl halides; Dehydrohalogenation; Elimination; Tetrabutylammonium fluoride

Indexed keywords

ALKYL HALIDES; DEHYDROHALOGENATION; ELIMINATION; TETRABUTYLAMMONIUM FLUORIDES;

AMMONIUM COMPOUNDS; FLUORIDE MINERALS; HALOGENATION; OPTIMIZATION; REACTION KINETICS; SYNTHESIS (CHEMICAL); THERMAL EFFECTS;

OLEFINS;

1 BROMO 3 (2' BROMOETHYL)BENZENE; 1 BROMO 3 (2' IODOETHYL)BENZENE; 11 IODOUNDECAN 1 OL; 11 IODOUNDECANAMIDE; 11 IODOUNDECANOIC AACID BUTYLMETHYLAMIDE; 12 IODODECAN 2 ONE; 12 IODODECANE; 12 IODODECANOIC ACID; 2 (9 IODONONYL)OXIRANE; 2 BROMODODECANE; 2 IODODODECANE; ALKENE DERIVATIVE; DIMETHYL SULFOXIDE; IODIDE; METHYL 12 IODODODECANOATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELIMINATION REACTION; HALOGENATION; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; SYNTHESIS;

EID: 33749525000     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-950204     Document Type: Article

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