Issue 24, 1991

Alkylation of 4H,6H-thieno[3,4-c]furan 5,5-dioxide and its use as a 3,4-dimethylenefuran synthon in intramolecular Diels–Alder reactions

Abstract

4H,6H-thieno[3,4-c]furan 5,5-dioxide 1 was readily converted to the 4-alkylated compounds 2 and the appropriate compounds 2 were submitted to intramolecular Diels–Alder reactions to afford fused furans 8a and b in good yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1765-1767

Alkylation of 4H,6H-thieno[3,4-c]furan 5,5-dioxide and its use as a 3,4-dimethylenefuran synthon in intramolecular Diels–Alder reactions

K. Ando, N. Akadegawa and H. Takayama, J. Chem. Soc., Chem. Commun., 1991, 1765 DOI: 10.1039/C39910001765

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