首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >An Efficient Synthesis of Benzo[ gg ]thiazolo[2,3‐ bb ]quinazolin‐4‐ium and Benzo[ gg ]benzo[4,5]thiazolo[2,3‐ bb ]quinazolin‐14‐ium Hydroxides by a One‐pot, Three‐component Reaction under Green Conditions
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An Efficient Synthesis of Benzo[ gg ]thiazolo[2,3‐ bb ]quinazolin‐4‐ium and Benzo[ gg ]benzo[4,5]thiazolo[2,3‐ bb ]quinazolin‐14‐ium Hydroxides by a One‐pot, Three‐component Reaction under Green Conditions

机译:有效的苯并合成[ g g ]噻唑[2,3- b b ]喹唑啉-4-Ium和Benzo [ g g ]苯并[4,5]噻唑洛[2,3- b b ]喹唑啉-14-1 14-Ium氢氧化物通过单罐,三组分反应在绿色条件下

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摘要

> A new series of benzo[ g ]thiazolo[2,3‐ b ]quinazolin‐4‐ium and benzo[ g ]benzo[4,5]thiazolo[2,3‐ b ]quinazolin‐14‐ium hydroxide derivatives have been synthesized by the one‐pot, three‐component reaction of aryl glyoxal monohydrates, 2‐hydroxy‐1,4‐naphthoquinone, and 2‐aminothiazole or 2‐aminobenzothiazole in the presence of triethylamine and p ‐toluenesulfonic acid as organocatalysts in H 2 O/acetone (2:1) at room temperature. This method offers mild reaction conditions, excellent yields, easy workup, and readily accessible starting materials and catalysts.
机译: > 一系列新系列苯并[ g ]噻唑[2,3- b ]喹唑啉-4-Ium和Benzo [ g ]苯并[4,5]噻唑洛[2,3- b 喹唑啉-14-1氢氧化物衍生物已经通过一锅,芳基乙二醛一水合物,2-羟基-1,4-萘醌和2-氨基噻唑或2-氨基噻唑或2-氨基异口唑在三乙胺的情况下合成 p -toluenesulfonic酸作为有机催化剂 2 室温下O /丙酮(2:1)。 该方法提供温和的反应条件,优异的产率,易于余处,易于接近的起始材料和催化剂。

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