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    题名 作者 年代 出处 被引量
1环状磷酸催化合成2-取代苯并咪唑显示文摘以邻苯二胺和醛为原料,四氢呋喃为溶剂,在环状磷酸催化下,室温下合成了一系列2-取代苯并咪唑化合物.考察了催化剂种类、用量和溶剂对反应的影响,确定了最优反应条件,提出了可能的反应机理.该反应具有操作简单,条件温和,产率高及环境友好等优点.王湘波 简腾跃 马晓伟 何林 2012有机化学2012,32,11:1
2Preparation of 1-amidoalkyl-2-naphthol derivatives using barium phosphate nano-powders显示文摘Barium phosphate(Ba_3(PO_4)_2) nano-powder was successfully synthesized via a simple precipitation route without any surfactant. The prepared nano-powder was applied for the facile synthesis of 1-amidoalkyl-2-naphthol derivatives using multi-component reaction of aldehydes, 2-naphthol and an amide(or urea) in high yields.Hadi Taghrir Majid Ghashang Mohammad Najafi Biregan 2016Chinese Chemical Letters2016,27,1:1
3无溶剂条件下三聚氰胺-Br_3催化一锅法合成1-氨基烷基-2-萘酚(英文)显示文摘A facile and efficient method has been developed for the synthesis of 1-amidoalkyl-2-naphthols via the one-pot multi-component condensation of 2-naphthol with aromatic aldehydes and acetamide or thioacetamide in the presence of melamine-Br3 under solvent-free conditions. There are several advantages to this reaction, including high yields, short reaction time, and high catalytic efficiency.Arash Ghorbani-Choghamarani Shima Rashidimoghadam 2014催化学报2014,35,7:1
4无溶剂条件下碳基固体酸催化一锅法合成酰胺烷基萘酚(英文)显示文摘An efficient, environmentally friendly procedure for the synthesis of amidoalkyl naphthols through the one‐pot, three‐component reaction of β‐naphthol, aryl aldehydes, and acetamide in the presence of a carbon‐based solid acid under thermal solvent‐free conditions is described. The beneficial fea-tures of this new synthetic approach include short reaction time, high yields, clean reaction profiles, and a simple work‐up procedure. Furthermore, the catalyst can be readily recycled and reused four times without obvious significant loss of activity. The structure of the catalyst was confirmed by Fourier transform infrared spectroscopy, N2 adsorption/desorption analysis, and X‐ray diffraction.Abolghasem Davoodnia Rahil Mahjoobin Niloofar Tavakoli-Hoseini 2014催化学报2014,35,4:1
5One-pot Combinatorial Synthesis of Benzo[4,5]imidazo- [1,2-a]thiopyrano[3,4-dJpyrimidin-4(3H)-one Derivatives显示文摘沈士德 张红红 杨伟华 于晨侠 姚昌盛 2011Chinese Journal of Chemistry2011,29,8:0
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