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Communication | Regular issue | Vol 26, No. 11, 1987, pp.2861-2864
Published online, 1st January, 1970
DOI: 10.3987/R-1987-11-2861
Thermal Rearrangements of 8-Aza- and 8-Oxa-3,4-diazatricyclo-[5.1.0.02.6]oct-4-enes

Jyoji Kurita, Hiroichi Sakai, and Takashi Tsuchiya

*School of Pharmacy, Hokuriku University, 3-Ho, Kanagawa machi, Kanazawa 920-1181, Japan

Abstract

Flash vacuum pyrolysis of the 8-oxa-3,4-diazatricyclo-[5.1.0.02,6]oct-4-enes (7) resulted in rearrangement to give the - 1-amino-2-formylpyrroles (7), presumably via the 1,4,5-oxadiazocines (14)whereas that of the 8-aza analogues (8) gave the 3a,6a-dihydropyrrolo[2,3-clpyrazoles (12) by a different type of rearrangement.