A novel approach to functionalized polycyclic systems; Synthesis of tetracyclic compounds by sequential rearrangement-cycloaddition reactions of 7-oxa-2,3-dimethylenenorbornene derivative

The tricyclic diene (6), readily accessible from a novel building block, 4H, 6H-thieno[3,4-c]furan 5,5-dioxide (1), reacted with a variety of dienophiles to give the tetracyclic perhydroazulene derivatives (7) in good to high yield.

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Bibliographic Details
Published inHeterocycles Vol. 47; no. 1; pp. 167 - 170
Main Authors Konno, K, Tanigawa, H, Takayama, K
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier 01.01.1998
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Summary:The tricyclic diene (6), readily accessible from a novel building block, 4H, 6H-thieno[3,4-c]furan 5,5-dioxide (1), reacted with a variety of dienophiles to give the tetracyclic perhydroazulene derivatives (7) in good to high yield.
ISSN:0385-5414
DOI:10.3987/com-97-s(n)72