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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis of fused tetrahydro-beta-carbolinequinoxalinones in 1-n-butyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)-imide([bdmim][Tf_2N])and l-n-butyl-2,3-dimethylimidazolium perfluorobutylsulfonate([bdmim][PFBuSO_3])ionic liquids
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Synthesis of fused tetrahydro-beta-carbolinequinoxalinones in 1-n-butyl-2,3-dimethylimidazolium bis(trifluoromethylsulfonyl)-imide([bdmim][Tf_2N])and l-n-butyl-2,3-dimethylimidazolium perfluorobutylsulfonate([bdmim][PFBuSO_3])ionic liquids

机译:在1-正丁基-2,3-二甲基咪唑双(三氟甲基磺酰基)-亚胺([bdmim] [Tf_2N])和正丁基-2,3-二甲基咪唑全氟丁基磺酸盐([bdmim] [ PFBuSO_3])离子液体

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摘要

Starting from tryptophan methyl ester,a three-step synthesis of fused tetrahydro-beta-carbolinequinoxalinones in two new ionic liquids,[bdmim][Tf_2N] and [bdmim][PFBuSO_3],was described.Both ionic liquids can be readily prepared from commercially available starting materials in high yields.Unlike the commonly used [PF_6]-based ionic liquids that evidently undergo slow hydrolysis of the PF_6 anion with the concomitant release of HF,ionic liquids of [bdmim][Tf_2N] and [bdmim][PFBuSO_3] are not only chemically stable but also apparently inert to hydrolysis and therefore organic reactions carried out in both ionic liquids proceed smoothly with good yields.The overall isolated yields for this three-step synthesis of tetrahydro-beta-carbolinequinoxalinones were 34-55%.To the best of our knowledge,the preparation of fused tetrahydro-beta-carbolinequinoxalinones was unprecedented.
机译:从色氨酸甲酯开始,描述了在两种新的离子液体[bdmim] [Tf_2N]和[bdmim] [PFBuSO_3]中三步合成稠合的四氢-β-咔啉喹喔啉酮的方法。 [bdmim] [Tf_2N]和[bdmim] [PFBuSO_3]的离子液体与常用的[PF_6]基离子液体明显会缓慢水解PF_6阴离子并伴随释放HF的离子液体不同。不仅在化学上稳定,而且对水解显然是惰性的,因此在两种离子液体中进行的有机反应均能顺利进行,并具有良好的收率。该三步合成四氢-β-咔啉喹喔啉酮的总分离收率为34-55%。据我们所知,熔融四氢-β-咔啉喹喔啉酮的制备是空前的。

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