Two tricyclic adducts from consecutive additions of dimethyl acetylene-dicarboxylate to 2,4-di-t-butyl-3a,5a-dihydro-3H-cyclobuta[b]pyrrole: A novel formation of cyclobuta[1',2'-f]pyrrolo-[1,2-b]oxazine derivative

Shizuka Takami, Kyosuke Satake, Masaru Kimura

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The tricyclic heterocycles (2) and (3) were newly synthesized by the addition reaction between 2,4-di-t-butyl-3a,5a-dihydro-3H-cyclobuta[b]pyrrole (1) and dimethyl acetylenedicarboxylate (DMAD). The structures were confirmed by the X-Ray structural analyses, and the pathway affording them was also proposed.

    Original languageEnglish
    Pages (from-to)775-780
    Number of pages6
    JournalHeterocycles
    Volume55
    Issue number4
    DOIs
    Publication statusPublished - Apr 1 2001

    ASJC Scopus subject areas

    • Analytical Chemistry
    • Pharmacology
    • Organic Chemistry

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