An efficient access to (Z)-β-fluoroallyl alcohols based on the two carbon homologation of aromatic aldehydes by Horner-Wadsworth-Emmons reaction with 2-(diethoxyphosphinyl)-2-fluoro-ethanethioic acid, S-ethyl ester followed by reduction with sodium borohydride

Tetrahedron

Volumn 68, Issue 15, 2012, Pages 3225-3230

  Kajjout, Mohammed ^a   Zemmouri, Rajae ^a   Eddarir, Said ^a,b   Rolando, Christian ^a  

^a University Lille   (France)

^b FACULTÉ DES SCIENCES ET TECHNIQUES GUÉLIZ   (Morocco)

Author keywords

Fluorothioesters; (Z) Fluoroallyl alcohols; Fluroconiferin; Horner Wadsworth Emmons; NaBH 4 reduction

Indexed keywords

2 (DIETHOXYPHOSPHINYL) 2 FLUORO ETHANETHIOIC ACID; ALDEHYDE; ALLYL ALCOHOL; ALPHA FLUOROCINNAMIC THIOESTER; BETA FLUOROALLYL ALCOHOL; ESTER DERIVATIVE; ISOMERASE; LIGNIN; LITHIUM; S ETHYL ESTER; SODIUM BOROHYDRIDE; THIOESTER; UNCLASSIFIED DRUG; VANILLIN DERIVATIVE;

ARTICLE; BIOMIMETICS; CONTROLLED STUDY; HORNER WADSWORTH EMMONS REACTION; ISOMERIZATION; POLYMERIZATION; PRIORITY JOURNAL; REDUCTION; ROOM TEMPERATURE;

EID: 84858706665     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.02.039     Document Type: Article

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