178496-33-8Relevant academic research and scientific papers
Biology-based flame-retardant epoxy resin precursor on basis of natural phenol monomers, method for preparing biology-based flame-retardant epoxy resin precursor and application thereof
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Paragraph 0049; 0050; 0054; 0055; 0059; 0060, (2019/05/22)
The invention discloses a biology-based flame-retardant epoxy resin precursor on the basis of natural phenol monomers. The biology-based flame-retardant epoxy resin precursor is of a structure shown as a following formula (I). A method for preparing the b
Metal-free synthesis of calixsalen-type cavitands for the recognition of fluoride ion
Desai, Arpita,Rana, Dharti
supporting information, p. 291 - 301 (2018/02/09)
Novel calixsalen-type cavitands have been synthesized using metal-free synthesis from simple and inexpensive materials, such as ethylenediamine and 5,5′-methylene-bis-salicylaldehyde derivatives. The cavitand 1 containing salen functionality recognizes fl
Synthesis and biological evaluation of a novel series of bis-salicylaldehydes as mushroom tyrosinase inhibitors
Delogu, Giovanna,Podda, Gianni,Corda, Marcella,Fadda, Maria Benedetta,Fais, Antonella,Era, Benedetta
body text, p. 6138 - 6140 (2010/11/18)
A series of novel bis-salicylaldehydes were synthesised and evaluated as tyrosinase inhibitors using a tyrosinase-dependent l-DOPA oxidation assay. The bis-salicylaldehydes exhibited greater inhibitory activity than salicylaldehyde. Our data suggests that
Synthesis of some 6,6'-methylene- and 6,6'-sulphone-biscoumarins
Brahmbhatt, D. I.,Jayabalan, L.,Hirani, B. R.,Singh, Shashibala
, p. 683 - 685 (2007/10/03)
Various 3,3'-disubstituted-6,6'-methylenebiscoumarins 3a-3d, 3,3'-disubstituted-8,8'-dimethoxy-6,6'-methylenebiscoumarins 3e-h and 3,3'-disubstituted-6,6'-sulphone-biscoumarins 3i-l have been synthesised by the reaction of appropriate bissalicylaldehydes
