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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >DEHYDROGENATIVE N-HETEROCYCLIZATION OF 2-(2-AMINOARYL)ETHYL ALCOHOLS TO INDOLE DERIVATIVES CATALYZED BY (μ-OXO)TETRARUTHENIUM CLUSTER/ l,2-BIS(DIPHENYLPHOSPHINO)BENZENE
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DEHYDROGENATIVE N-HETEROCYCLIZATION OF 2-(2-AMINOARYL)ETHYL ALCOHOLS TO INDOLE DERIVATIVES CATALYZED BY (μ-OXO)TETRARUTHENIUM CLUSTER/ l,2-BIS(DIPHENYLPHOSPHINO)BENZENE

机译:2-(2-氨基芳基)乙基醇在(μ-氧代)四钌簇簇/ l,2-双(二苯基膦基)苯催化下的加氢N-杂环化为吲哚衍生物

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摘要

A novel catalyst system of (μ-oxo)tetraruthenium cluster (2) combined with l,2-bis(diphenylphosphino)benzene (dppbz) realized a simple, selective, and practical synthesis of indole and its derivatives from 2-(2-aminoaryl)ethyl alcohols via dehydrogenative N-heterocyclization reaction. Spontaneous formation of a stoichiometric amount of hydrogen (H2) was observed, and the present reaction proceeded smoothly under an argon atmosphere without oxidants and/or hydrogen acceptors.
机译:(μ-氧代)四钌簇(2)与1,2-双(二苯基膦基)苯(dppbz)结合的新型催化剂体系实现了由2-(2-氨基芳基)简单,选择性和实用的合成吲哚及其衍生物醇通过脱氢N-杂环反应。观察到自发形成化学计算量的氢(H 2),并且本反应在氩气气氛下平稳地进行,没有氧化剂和/或氢受体。

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