An efficient one-pot synthesis of oxime ethers from alcohols using triphenylphosphine/carbon tetrachloride

Synthesis

Volumn , Issue 10, 2010, Pages 1724-1730

  Soltani Rad, Mohammad Navid ^a   Khalafi Nezhad, Ali ^b   Karimitabar, Fatemeh ^b   Behrouz, Somayeh ^a  

^a SHIRAZ UNIVERSITY OF TECHNOLOGY   (Iran)

^b SHIRAZ UNIVERSITY   (Iran)

Author keywords

Alcohol; Carbon tetrachloride; DBU; O alkylation; Oxime; Triphenylphosphine

Indexed keywords

ALKYL ETHERS; CATALYTIC AMOUNTS; GOOD YIELD; HEAT OF FORMATION; O-ALKYLATION; ONE POT; ONE-POT SYNTHESIS; OXIME ETHERS; REFLUXING; SEMI-EMPIRICAL; TETRABUTYLAMMONIUM; TRIPHENYL PHOSPHINES; UNSYMMETRICAL;

ACETONITRILE; CARBON TETRACHLORIDE; ETHERS; ISOMERS; SYNTHESIS (CHEMICAL); THERMOCHEMISTRY;

ALKYLATION;

ACETONITRILE; ALCOHOL DERIVATIVE; CARBON TETRACHLORIDE; OXIME; OXIME DERIVATIVE; OXIME ETHER; TETRABUTYLAMMONIUM; TRIPHENYLPHOSPHINE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL REACTION; ONE POT SYNTHESIS; QUANTUM MECHANICS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 77952042495     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1218711     Document Type: Article

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