102692-40-0Relevant articles and documents
Monofunctionalized 1,3,5,7-tetraarylazaBODIPYs and their application in the synthesis of AzaBODIPY based conjugates
Koch, Angira,Ravikanth, Mangalampalli
, p. 10775 - 10784 (2019)
A series of monofunctionalized 1,3,5,7-tetraarylazaBODIPYs containing functional groups such as p-hydroxymethyl phenyl, p-hydroxyphenyl, p-cyanophenyl, p-nitrophenyl, and p-formylphenyl groups at the 1-position of the azaBODIPY core were synthesized by mi
Lewis acid catalyst system for Claisen-Schmidt reaction under solvent free condition
Halpani, Chandni G.,Mishra, Satyendra
, (2020)
Ca(OTf)2 in combination with NBu4.BF4 was established to function as an efficient catalyst system for one-pot Claisen-Schmidt condensation under neat conditions. Substituted acetophenones and benzaldehydes were coupled in situ to afford their corresponding chalcones in excellent yields. The method, with a broad range of substrate tolerance and mild operational conditions can produce assorted chalcone derivatives in moderate to high yields from easily accessible starting materials.
Monoamine Oxidase Inhibitory Activity: Methyl- versus Chlorochalcone Derivatives
Mathew, Bijo,U?ar, Gülberk,Mathew, Githa Elizabeth,Mathew, Sincy,Kalatharakkal Purapurath, Praseedha,Moolayil, Fasil,Mohan, Smrithy,Varghese Gupta, Sheeba
, p. 2649 - 2655 (2016/12/23)
Numerous studies have shown that chalcones are promising scaffolds for the development of new monoamine oxidase-B (MAO-B) inhibitors. As a continuation of our ongoing research into the development of reversible human MAO-B (hMAO-B) inhibitors, two series