55485-77-3Relevant academic research and scientific papers
A mild and one-step synthesis of 2,8-dioxabicyclo [3.3.1] nonane derivatives via classical Knoevenagel condensation
Yang, De-Suo,Ke, Sen,Du, Xin,Gao, Peng,Zhu, Hai-Tao,Fan, Ming-Jin
, p. 5522 - 5527 (2017)
Utilizing simple and readily available 2-hydroxy benzaldehydes and 1,3-diketones or 1,3-cyclohexanediones as raw materials, complex 2,8-dioxabicyclo [3.3.1] nonane derivatives were synthesized in one-step via classical Knoevenagel condensation. The reaction was simply conducted under solvent-free and mild conditions, which showed good tolerance to a variety of functional groups. This atom-economical approach delivers an attractive synthetic protocol for 2,8-dioxabicyclo [3.3.1] nonane derivatives.
Microwave Oriented Solid Support Synthesis of Novel 5,6-Disubstituted-1,2,4-Triazolopyrimidines as Antifungal Agents
Bala, Anju,Gumber, Khushbu,Sidhu, Anjali,Sidhu, Navjot Kaur
, p. 39 - 46 (2021/06/12)
Microwave oriented, basic solid support assisted, two-step reaction of aryl aldehyde, active methylene compounds, and 3-amino-1,2,4-triazole yielded 5,6-disubstituted-1,2,4-triazolopyrimidines in excellent yield without side products, in short reaction time. The preliminary in vitro antifungal evaluation of the compounds indicated the promising antifungal potential of the synthesized compounds against most of the test fungi using standard fungicides as a positive control. The in silico analysis of the synthesized molecules favors the results of in vitro analysis.
