Regioselective synthesis of (E)-5-(tributylstannylmethylidene)-5H-furan-2- ones and (E)-3-(tributylstannylmethylidene)-3H-isobenzofuran-1-ones: Easy access to γ-alkylidenebutenolide and phthalide skeletons

Synthesis

Volumn , Issue 4, 2007, Pages 597-607

  Duchêne, Alain ^a   Thibonnet, Jérôme ^a   Parrain, Jean Luc ^b   Anselmi, Elsa ^a   Abarbri, Mohamed ^a  

^a EA 3857   (France)

^b Laboratoire Symbio   (France)

Author keywords

Alkylidenebutenolides; Cross coupling; Cyclisation; Phthalides; Retinoids

Indexed keywords

ALKYLIDENEBUTENOLIDES; CROSS-COUPLING; PHTHALIDES; RETINOIDS;

CATALYSIS; CHEMICAL BONDS; CYCLIZATION; IODINE COMPOUNDS; SYNTHESIS (CHEMICAL);

OLEFINS;

3 (3 METHYLBUT 2 ENYLIDENE) (3H) ISOBENZOFURAN 2 ONE; 3 [3 PHENYLALLYLIDENE] (3H) ISOBENZOFURAN 1 ONE; 3 BENZYLIDENE 3H ISOBENZOFURAN 2 ONE; 3 CHLOROALLYLIDENE 5H FURAN 2 ONE; 3 IODOMETHYLIDENENEPHTHALIDE; 3 PHENYLALLYLIDENE 5H FURAN 2 ONE; 3 TRIBUTYLSTANNYLMETHYLIDENEPHTHALIDE; 4 METHYL 5 [3 (TRIMETHYLSILYL)PROP 2 YNYLIDENE] FURAN 2 ONE; 4 METHYL 5 [3 METHYL 5 (2,6,6 TRIMETHYLCYCLOHE 1 ENYL)PENTA 2,4 DIENYLIDENE] (5H) FURAN 2 ONE; 4 METHYL 5 [5 (2,6,6 TRIMETHYLCYCLOHEX 2 ENYL)PENT 4 EN 2 YNYLIDENE] (5H) FURAN 2 ONE; 4 METHYL 5 [5 (TRIMETHYLSILOXY)PENT 2 YNYLIDENE] FURAN 2 ONE; 4 METHYL 5 IDODOMETHYLIDENE 5H FURAN 2 ONE; 4 METHYL 5 METHYLIDENE 5H FURAN 2 ONE; 5 (2 NITROBENZYLIDENE 5H FURAN 2 ONE; 5 (3 METHYLBUT 2 ENYLIDENE)FURAN 2 (5H) ONE; 5 [(PYRIDIN 2 YL)METHYLENE] 5H FURAN 2 ONE; 5 [(THIOPHEN 2 YL)METHYLIDENE] 5H FURAN 2 ONE; 5 BENZYLIDENE 4 METHYL 5H FURAN 2 ONE; 5 BENZYLIDENE 5H FURAN 2 ONE; 5 IODOMEETHYLIDENE 5H FURAN 2 ONE; [3 (TRIMETHYLSILYL)ALLYLIDENE] (5H) FURAM 2 ONE; [3 (TRIMETHYLSILYL)ALLYLIDENE] 3H ISOBENZOFURAN 1 ONE; ACETYLENE DERIVATIVE; BUTENOLIDE; EXOCYCLIC DOUBLE BOND; FURAN DERIVATIVE; GAMMA ALKYLIDENEBUTENOLIDE; PALLADIUM; PHTHALIDE DERIVATIVE; TRIBUTYLTINACETYLENE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; CYCLIZATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 33947507100     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-965890     Document Type: Article

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