119337-30-3Relevant academic research and scientific papers
Synthesis, biological evaluation and molecular docking study of 1,2,3-1H-triazoles having 4H-pyrano[2,3-d]pyrimidine as potential Mycobacterium tuberculosis protein tyrosine phosphatase B inhibitors
Thanh, Nguyen Dinh,Hai, Do Son,Ha, Nguyen Thi Thu,Tung, Do Tien,Le, Cao Thi,Van, Hoang Thi Kim,Toan, Vu Ngoc,Toan, Duong Ngoc,Dang, Le Hai
, p. 164 - 171 (2018/12/13)
Some heterocycles, namely 2-amino-4H-pyran-3-carbonitriles, were synthesized in a three-component reaction from substituted benzaldehydes, malononitrile, and ethyl acetoacetate. These heterocycles have been converted subsequently into 4H-pyrano[2,3-d]pyri
Efficient and expeditious synthesis of pyrano-pyrimidines, multi-substituted γ-pyrans, and their antioxidant activity
El-Bayouki, Khairy A. M.,Basyouni, Wahid M.,Khatab, Tamer K.,El-Basyoni, Fakhry A.,Hamed, Ahmed R.,Mostafa, Eslam A.
, p. 106 - 115 (2014/02/14)
An efficient, expeditious catalytic route for the synthesis of ethyl 6-amino-5-cyano-2-methyl-4-aryl-4H-pyran-3-carboxylates 2 was achieved via a three-component, one-pot reaction of malononitrile, ethyl acetoacetate, and various aromatic aldehydes in wat
Polyazanaphthalenes, I. The Reaction of Ethyl 6-Amino-5-cyano-4-aryl-2-methyl-4H-pyran-3-carboxylate with Nucleophilic Reagents
Harb, Abdel-Fattah A.,Hesien, Abdel-Haleem M.,Metwally, Saoud A.,Elnagdi, Mohamed Hilmy
, p. 585 - 588 (2007/10/02)
Ethyl 6-amino-5-cyano-4-aryl-2-methyl-4H-pyran-3-carboxylates 4 could be converted into 1,6-diazanaphthalene, pyranopyrazole, isoxazolopyridine, pyranopyridine, 1,8-diazanaphthalene, and pyranopyridine derivatives on treatment
