29412-34-8Relevant academic research and scientific papers
Synthesis, molecular modeling and biological evaluation of aza-flavanones as α-glucosidase inhibitors
Kasturi, Sivaprasad,Surarapu, Sujatha,Bathoju, Chandra Chary,Uppalanchi, Srinivas,Dwivedi, Shubham,Perumal, Yogeeswari,Sigalapalli, Dilep Kumar,Babu, Bathini Nagendra,Ethiraj, Krishna S.,Anireddy, Jaya Shree
, p. 1618 - 1630 (2017/08/22)
An efficient acid catalyzed methodology has been employed to synthesize a variety of aza-flavanones and their α-glucosidase inhibitory activity is evaluated using acarbose, miglitol and voglibose as reference standards. Molecular modeling studies were per
Tandem synthesis of pyrrolo[2,3-b]quinolones via cadogen-type reaction
Lin, Zhichen,Hu, Zhongyan,Zhang, Xin,Dong, Jinhuan,Liu, Jian-Biao,Chen, De-Zhan,Xu, Xianxiu
supporting information, p. 5284 - 5287 (2017/11/06)
A tandem [3 + 2] cycloaddition/reductive cyclization of nitrochalcones with activated methylene isocyanides for the efficient synthesis of pyrrolo[2,3-b]- quinolones is reported. In this reaction, the in situ generated dihydropyrroline acts as the interna
Efficient construction of 3-arylquinolin-4(1H)-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides
Wang, Sheng,Zhao, Chao,Liu, Ting,Yu, Lifang,Yang, Fan,Tang, Jie
, p. 7025 - 7031 (2016/10/14)
An efficient method for construction of 3-arylquinolin-4(1H)-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides has been developed. The practical approach is of excellent functional groups compatibili
