首页> 外文期刊>Journal of Molecular Structure >Highly functionalized dispiro oxindole-pyrrolo[1,2-c]thiazole-piperidone hybrid: Synthesis, characterization and theoretical investigations on the regiochemistry
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Highly functionalized dispiro oxindole-pyrrolo[1,2-c]thiazole-piperidone hybrid: Synthesis, characterization and theoretical investigations on the regiochemistry

机译:高度功能化的二螺氧杂吲哚-吡咯并[1,2-c]噻唑-哌啶酮杂化物:区域化学的合成,表征及理论研究

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The synthesis of highly functionalized dispiro oxindole-pyrrolo[1,2-c]thiazole-piperidone hybrid has been achieved regioselectively employing microwave-assisted three-component 1,3-dipolar cycloaddition. Structural elucidation of the compound has been accomplished using NMR spectroscopy and further confirmed by single crystal X-ray crystallographic studies. The molecular structure of the compound crystallized in monoclinic, P2(1)/c, a = 11.6182 (2) angstrom, b = 12.2466 (2) angstrom, c = 21.7061 (3) angstrom, beta = 103.018 (1)degrees, V = 3009.04 (8) angstrom(3), Z = 4. The cycloaddition was found to proceed by normal electronic demand (NED) character with a significant high charge transfer (0.1247 eV) from the 1,3-dipole to the dipolarophile. The regiochemistry has been explained using the local reactivity descriptors obtained from the DFT calculations. The DFT optimized molecular structure agreed well with the X-ray results. (C) 2016 Elsevier B.V. All rights reserved.
机译:利用微波辅助的三组分1,3-偶极环加成反应可以区域选择性地合成高度官能化的双螺并氧杂吲哚-吡咯并[1,2-c]噻唑-哌啶酮。该化合物的结构阐明已使用NMR光谱学完成,并已通过单晶X射线晶体学研究进一步证实。以单斜晶结晶的化合物的分子结构,P2(1)/ c,a = 11.6182(2)埃,b = 12.2466(2)埃,c = 21.7061(3)埃,β= 103.018(1)度,V = 3009.04(8)埃(3),Z =4。发现环加成反应是通过正常的电子需求(NED)特性进行的,从1,3-偶极子到亲偶极子的电荷转移很高(0.1247 eV)。已经使用从DFT计算获得的局部反应性描述符解释了区域化学。 DFT优化的分子结构与X射线结果非常吻合。 (C)2016 Elsevier B.V.保留所有权利。

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