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SYNTHESES AND REGIOSELECTIVE CYCLOADDITION REACTIONS OF CYCLOHEPT-IMIDAZOIMIDAZOLES (1,3a,9-TRIAZACYCLOPENTAZULENES) :FORMATION OF 2,3-DIAZACYCLOHEPTACYCLAZINE SYSTEM

DOI: 10.1246/cl.1982.805

Source and publish data:

Chemistry Letters p. 805 - 806 (1982)

Update date:2022-08-04

Topics:

Authors:

Abe, Noritaka

Nishiwaki, Tarozaemon

Yamamoto, Hideko

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Article abstract of DOI:10.1246/cl.1982.805

Cycloheptimidazo<1,2-a>imidazoles (1,3a,9-triazacyclopent-azulenes), being synthesized from 2-aminocycloheptimidazole, was allowed to react with reactive acetylenes to give 2,3-diazacyclohepta-cycl<3.2.2>azines regioselectively.

Full text of DOI:10.1246/cl.1982.805

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Product name:2-amino-1-phenacylcycloheptimidazole hydrobromide

Cas No:82673-92-5

82673-92-5

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