首页> 外文期刊>Journal of Organometallic Chemistry >Reaction of alkoxycarbene complexes of tungsten with 1,2-dlhydroquinoline: single vs. double hydride transfers to the carbene-carbon: synthesis, X-ray structure and reactivity of a quinolinium ylide complex of tungsten pentacarbonyl
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Reaction of alkoxycarbene complexes of tungsten with 1,2-dlhydroquinoline: single vs. double hydride transfers to the carbene-carbon: synthesis, X-ray structure and reactivity of a quinolinium ylide complex of tungsten pentacarbonyl

机译:钨的烷氧基卡宾配合物与1,2-二氢喹啉的反应:单氢化物与双氢化物转移至卡宾碳:五羰基钨的喹啉鎓叶立德配合物的合成,X射线结构和反应性

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摘要

The more stable dihydropyridine, 1,2-dihydroquinoline (2), reacts with carbene complex of tungsten (CO)(5)W=(OEt)Ph (3) to give the expected quinolinium complex 4, fully characterized by an X-ray structure. By contrast, under the same conditions complex 7 (CO)(5)W=(OEt)Me led to the alkyltungstate 15 as the result of a double hydride transfer to the carbene-carbon. Complex 15 could be trapped by the enamine of morpholine and cyclohexanone and gave the addition product 14. The quinoline in 4 is easily exchangeable by excess pyridine, via a dissociative mechanism, and gives the known pyridinium ylide complex 5. (C) 2003 Elsevier B.V. All rights reserved. [References: 25]
机译:较稳定的二氢吡啶1,2-二氢喹啉(2)与钨(CO)(5)W =(OEt)Ph(3)的卡宾配合物反应生成预期的喹啉配合物4,其特征在于X射线结构体。相反,在相同条件下,由于双氢化物转移至卡宾碳,络合物7(CO)(5)W =(OEt)Me导致生成钨酸烷基酯15。配合物15可以被吗啉和环己酮的烯胺截留,得到加成产物14。4中的喹啉通过离解机理很容易与过量的吡啶交换,得到已知的吡啶鎓叶立德配合物5。(C)2003 Elsevier BV版权所有。 [参考:25]

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