首页> 外文期刊>Chemistry: A European journal >Gold(I)-catalyzed 6-endo-dig hydrative cyclization of an alkyne-tethered ynamide: Access to 1,6-dihydropyridin-2(3H)ones
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Gold(I)-catalyzed 6-endo-dig hydrative cyclization of an alkyne-tethered ynamide: Access to 1,6-dihydropyridin-2(3H)ones

机译:金(I)催化的炔烃拴住的酰胺的6-内-挖水合环化:获得1,6-二氢吡啶-2(3H)酮

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摘要

Hydrate your chemistry! Hydrative cyclization of 5-yne-ynamides in the presence of Echavarren's catalyst and p-toluenesulphonic acid (PTSA)×H_2O at room temperature affords an array of 1,6-dihydropyridin-2(3H)one derivatives. Isomerization, epoxidation, and hydrogenation of the double bond and insertion of an extended π-conjugate system into the pyridinone skeleton have been successfully accomplished (see scheme; Ts=tosyl).
机译:补充您的化学物质!在室温下,在Echavarren's催化剂和对甲苯磺酸(PTSA)×H_2O的存在下,对5-炔基酰胺进行水合环化反应,得到了一系列的1,6-二氢吡啶-2(3H)one衍生物。已成功完成双键的异构化,环氧化和加氢反应,以及将扩展的π共轭体系插入吡啶酮骨架中(参见方案; Ts =甲苯磺酰基)。

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