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A Novel Method for Synthesis of Tetrahydro-2//-oxazolo[2,3-a]isoquinolines

机译:一种合成四氢-2 // - 恶唑的新方法[2,3-a]异喹啉

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摘要

An efficient and direct method for the synthesis of tetrahydro-2H-oxazolo[2,3-<2]isoquinolines is reported.This novel method involves ~RT3P mediated in situ oxidation of benzyl alcohols to aldehyde followed by acetic acid mediated [3+2] cycloaddition reaction to afford tetrahydro-2H-oxazolo[2,3-a]isoquinolines in one-pot operation with good to excellent yields.Heterocyclic alcohols also underwent the reaction with tetrahydroquinolines at room temperature.
机译:报道了一种用于合成四氢-2H-恶唑的高效和直接方法[2,3- <2]异喹啉。该新方法涉及〜RT3P原位氧化苄醇氧化至醛,然后介导乙酸介导[3 + 2 环加成反应,得到四氢-2H-恶唑,在单盆手术中得到良好的优异产率.HerciClic醇也在室温下与四氢喹啉进行反应。

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