One-pot synthesis of tetrahydrofuran derivatives via a divalent palladium-catalyzed three-component coupling

Tetrahedron Letters

Volumn 44, Issue 3, 2003, Pages 467-470

  Liu, Guosheng ^a   Lu, Xiyan ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

heteroatom elimination; Carbopalladation; Coupling reaction; Divalent palladium; Tetrahydrofuran derivatives

Indexed keywords

ALKENE DERIVATIVE; ALKYNE; CHLORIDE; PALLADIUM; TETRAHYDROFURAN DERIVATIVE;

ARTICLE; CARBOPALLADATION; CATALYSIS; CATALYST; CHEMICAL BOND; CHEMICAL REACTION; CYCLIZATION; DIASTEREOISOMER; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

INSERTION SEQUENCES;

EID: 0037433966     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02604-7     Document Type: Article

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17. A similar strategy has been used to synthesize tetrahydrofuran derivatives under Pd(0) catalysis, see: (a) Monteiro, N.; Balme, G. J. Org. Chem. 2000, 65, 3223; (b) Bottex, M.; Cavicchioli, M.; Hartmann, B.; Monteiro, N.; Balme, G. J. Org. Chem. 2001, 66, 175.
18. A similar strategy has been used to synthesize tetrahydrofuran derivatives under Pd(0) catalysis, see: (a) Monteiro, N.; Balme, G. J. Org. Chem. 2000, 65, 3223; (b) Bottex, M.; Cavicchioli, M.; Hartmann, B.; Monteiro, N.; Balme, G. J. Org. Chem. 2001, 66, 175.
19. 5, 316.1311. Found: 316.1326. The stereochemistry of 3a was determined by NOESY spectra.