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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Convenient Preparation of Heteroazulenes by the Reaction of 2-Aminotropone with Hetreocumulenes in the Presence of a Base
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Convenient Preparation of Heteroazulenes by the Reaction of 2-Aminotropone with Hetreocumulenes in the Presence of a Base

机译:在碱存在下,2-氨基苯醌与杂枯草酮反应可方便地制备杂杂唑

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摘要

Reactions of 2-aminotropone with heterocumulenes, N,N'-diphenylcarbodiimide, phenyl isothiocyanate, phenyl isocyanate, and carbon disulfide, in the presence of t-BuOK afforded 1-phenylcycloheptaimidazole-2(1H)-phenylimine, 1-phenylcyclohepataimidazole-2(1H)-thione, 1-phenylcyclohepta-imidazol-2(1H)-one along with 2H-cycloheptaoxazol-2-one, and 2H-cycloheptathiazol-2-one along with 2H-cycloheptaoxazole-2-thione in good to moderate yields, respectively.
机译:在t-BuOK的存在下,2-氨基tropone与杂多烯,N,N'-二苯基碳二亚胺,苯基异硫氰酸酯,苯基异氰酸酯和二硫化碳的反应提供了1-苯基环庚二咪唑-2(1H)-苯基亚胺,1-苯基环庚二唑-2( 1H)-硫酮,1-苯基环庚-咪唑-2(1H)-一和2H-环庚恶唑-2-酮和2H-环庚二唑-2-一以及2H-环庚恶唑-2-硫酮的收率中等至中等,分别。

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