Regioselectivity in the reaction of ethyl diethoxyphosphorylacetate with 1-aryl-2-haloalkan-1-ones: Effective synthesis of 4-aryl-2-diethoxyphosphoryl-4- oxobutanoates

Synthesis

Volumn , Issue 11, 2007, Pages 1671-1676

  Koszuk, Jacek F ^a   Albrecht, Anna ^a   Janecki, Tomasz ^a  

^a LODZ UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

haloketones; Alkylations; Ethyl diethoxyphosphorylacetate; Horner Wadsworth Emmons olefination; Regioselectivity

Indexed keywords

ALPHA-HALOKETONES; ETHYL DIETHOXYPHOSPHORYLACETATE; HORNER-WADSWORTH-EMMONS OLEFINATION; REACTION CONDITIONS;

ALKYLATION; HALOGEN ELEMENTS; OLEFINS; ORGANIC COMPOUNDS; SYNTHESIS (CHEMICAL);

REGIOSELECTIVITY;

1 ARYL 2 HALOALKAN 1 ONE DERIVATIVE; 4 ARYL 2 DIETHOXYPHOSPHORYL 4 OXOBUTANOATE DERIVATIVE; ACETIC ACID DERIVATIVE; ALKANONE; BUTYRIC ACID DERIVATIVE; ETHYL DIETHOXYPHOSPHORYLACETATE; HALOGEN; UNCLASSIFIED DRUG;

ARTICLE; ATOM; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; DIASTEREOISOMER; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 34250317361     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-966060     Document Type: Article

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