Synthesis of 3-vinyl-2,5-dihydrofuran ring system via enyne metathesis

Carbohydrate Research

Volumn 345, Issue 2, 2010, Pages 324-329

  Vuong, Sophie ^a   Mercedes Rodriguez Fernandez, M ^a   Renoux, Brigitte ^a   Len, Christophe ^a  

^a UNIVERSITÉ DE POITIERS   (France)

Author keywords

Asymmetrical synthesis; Enyne metathesis; Glycosyl donor

Indexed keywords

ASYMMETRIC CARBONS; DIHYDROFURANS; ENYNE METATHESIS; GLYCOSYL DONORS; PROTON NMR; REACTIVE SUBSTRATES; RING SYSTEMS; TARGET COMPOUND;

ACETYLENE; METHANOL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RUTHENIUM;

SYNTHESIS (CHEMICAL);

5 ETHOXY 4 VINYL 2,5 DIHYDROFURAN 2 YL METHANOL; 5 ETHOXY 4 VINYL 2,5 DIHYDROFURAN 2 YLMETHOXY TERT BUTYLDIPHENYLSILANE; 5 ETHOXY 4 VINYL 2,5 DIHYDROFURAN 2 YLMETHOXY TRIPHENYLMETHANE; 5 ETHOXY 4 VINYL 2,5 DIHYDROFURAN 2 YLMETHYL ACETATE; 5 ETHOXY 4 VINYL 2,5 DIHYDROFURAN 2 YLMETHYL BENZOATE; CARBON; FURAN DERIVATIVE; RUTHENIUM; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; NUCLEAR OVERHAUSER EFFECT; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS;

ALKENES; ALKYNES; CARBON; FURANS; STEREOISOMERISM;

EID: 73049107966     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2009.09.023     Document Type: Article

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