904604-04-2Relevant academic research and scientific papers
A facile synthesis of pyrrolidine-based iminosugars as potential alpha-glucosidase inhibitors
Bacho, Muhamad Zulfaqar,Hamzah, Ahmad Sazali,Kamarulzaman, Firdaus,Mohammat, Mohd Fazli,Shaameri, Zurina,Wibowo, Agustono
, p. 309 - 319 (2020/07/03)
A multifaceted approach comprising MCR (multicomponent reaction), amination and stereoselective reduction reactions was used to synthesize new pyrrolidine-based iminosugars. The key step of this strategy involves the contruction of a highly functionalised
Synthesis and bioactivity of some 2-oxo-5-aryl-3-hydrazone and 2-oxo-5-aryl-4-hydrazone pyrrolidine derivatives
Mohammat, Mohd Fazli,Najim, Nigar,Mansor, Nurul Shulehaf,Sarman, Sharil,Shaameri, Zurina,Zain, Mazatulikhma Mat,Hamzah, Ahmad Sazali
experimental part, p. 429 - 438 (2011/12/05)
2-Aryl-4,5-dioxopyrrolidine-3-carboxylate and 5-aryl-2,4-dioxopyrrolidine- 3-carboxylate derivatives were successfully synthesized via carbonyl-based multiple component reaction and Dieckmann cyclization, respectively. Successive functional group transformations which include decarboxylation and hydrazonation afforded 2-oxo-5-aryl-3-hydrazone and 2-oxo-5-aryl-4-hydrazone derivatives. Compound 3d exhibited activity against human histiocytic lymphoma (U937) and neuroblastoma (SH-SY5Y) cell lines while compound 6 showed neuroprotective ability from oxidative stress medium induced with H2O2.
Synthesis of 2,3-dioxo-5-(substituted)arylpyrroles and their 2-oxo-5-aryl-3-hydrazone pyrrolidine derivatives
Mohammat,Shaameri,Hamzah
experimental part, p. 250 - 256 (2009/08/15)
Some novel 2,3-dioxo-5-(substituted)arylpyrroles have been synthesized. Among these, pyrrolidine compound 1b was converted to 2,3-dioxo-5-aryl pyrrolidine 2b. Finally a set of hydrazone derivatives was obtained from the reaction of 2b with various hydrazi
