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文多灵及其衍生物的结构与合成。

Structure and Synthesis of Vindolicine and Derivatives.

机构信息

H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Sindh, Pakistan.

UPR CNRS 8241, Laboratoire de Chimie de Coordination, 205 Route de Narbonne, 31077, Toulouse Cedex 04, France.

出版信息

Chem Biodivers. 2024 Apr;21(4):e202301928. doi: 10.1002/cbdv.202301928. Epub 2024 Feb 26.

Abstract

This article describes the reaction of vindoline with formaldehyde and trimethyl orthoformate to prepare vindolicine, tris-vindolicinyl methane and higher molecular weight homologues. The synthesis of 10-formyl vindoline as an intermediate allowed further exploration of its chemistry, in particular the reaction with acetone which yielded a symmetrical dimer, which was further reacted with vindoline to give molecules containing three and four vindoline units. These molecules were characterized by NMR and for some of them (vindolicine, 10-formyl vindoline, 10-(1'-(but-1'-en-3'-one))-vindoline) by X-ray crystallography. Depending on the substitution and on the absence of axes of symmetry, the NMR spectra displayed non-equivalent spin systems for the vindoline moieties. The dimer formed from the double condensation of 10-formyl vindoline with acetone showed cytotoxic activity in the micromolar range.

摘要

本文描述了文多灵与甲醛和三甲氧基甲烷的反应,以制备文多灵、三文多灵基甲烷和更高分子量的同系物。10-甲酰基文多灵作为中间体的合成允许进一步探索其化学性质,特别是与丙酮的反应,生成对称二聚体,进一步与文多灵反应得到含有三个和四个文多灵单元的分子。这些分子通过 NMR 进行了表征,对于其中一些分子(文多灵、10-甲酰基文多灵、10-(1'-(丁-1'-烯-3'-酮))-文多灵)通过 X 射线晶体学进行了表征。根据取代基和对称轴的缺失,NMR 谱显示文多灵部分的非等价自旋系统。由 10-甲酰基文多灵与丙酮的双重缩合形成的二聚体在微摩尔范围内表现出细胞毒性活性。

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