NMR spectral and structural studies on some xanthenones and their thiosemicarbazone derivatives: Crystal and molecular structure of 12-(2-chlorophenyl)-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one
摘要:
A series of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones [1a-9a] were prepared employing a three component one-pot reaction of aryl aldehyde, 2-naphthol and 1,3-cyclohexanedione using BF3 center dot OEt2 as catalyst. Thiosemicarbazone derivatives [1b-5b] were also prepared in the presence of acid catalyst. All the synthesized compounds have been characterized by IR and NMR. The structure of 5b was confirmed by HSQC spectral analysis. Single crystal X-ray structural analysis of 12-(2-chloropheny1)8,9,10,12-tetrahydrobenzo[a]xanthen-11-one evidences the envelope and flattened-boat conformations of cyclohexenone and pyran rings respectively. (C) 2011 Elsevier B.V. All rights reserved.
DOI:
10.1016/j.molstruc.2011.11.003
作为产物:
描述:
间溴苯甲醛 、 1,3-环己二酮 、 2-萘酚 在
chitosan modified with Fe3O4 and silver nanoparticles 作用下,
以
水 为溶剂,
反应 0.58h,
以90%的产率得到12-(3-bromophenyl)-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one
参考文献:
名称:
Chitosan synergistically enhanced by successive Fe3O4 and silver nanoparticles as a novel green catalyst in one-pot, three-component synthesis of tetrahydrobenzo[α]xanthene-11-ones