71827-79-7Relevant articles and documents
2,2′-(Arylmethylene)bis(3-hydroxy-5,5-dimethylcyclohex-2-enone) crystals formation via atom economy reaction and their antioxidant activity
Thakur, Deepa,Kaur, Manvinder,Malhi, Dharambeer Singh,Garg, Sonali,Sharma, Ajay,Sohal, Harvinder Singh
, p. 537 - 543 (2021/05/10)
Tetraketones with their diversified biological potencies became a highly significant class of oxygen-containing organic compounds. These are prepared by applying a simple Knoevenagel-Michael cascade procedure with 1,3-dicarbonyl compound and aldehydes. In
In water–ultrasound-promoted synthesis of tetraketones and 2-substituted-1H-benzimidazoles catalyzed by BiOCl nanoparticles
Sapkal, Bharatkumar M.,Labhane, Prakash K.,Satam, Jitendra R.
, p. 4967 - 4979 (2017/07/22)
A highly efficient, green protocol has been developed for the synthesis of various structurally diverse 2,2′-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) and 2-substituted-1H-benzimidazole derivatives. The reaction was performed in water under ultrasound irradiation, using BiOCl nanoparticles as a catalyst. The nanocatalyst was found to be reusable for seven subsequent reactions without much loss in activity. Simple methodology with short reaction times and mild reaction conditions with easy work-up procedure are the salient features of this method.
Domino Knoevenagel/Michael synthesis of 2,2’-arylmethylenebis(3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one) derivatives catalyzed by silica-diphenic acid and their single crystal X-ray analysis
Vaid, Rupali,Gupta, Monika,Kant, Rajni,Gupta, Vivek K
, p. 967 - 976 (2016/07/06)
An efficient and eco-friendly procedure has been developed for the synthesis of various 2,2’-arylmethylenebis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) derivatives which were isolated and characterized by melting point, IR, 1H-NMR, 13/s
