Umed Singh
University of Iowa(US)Indian Institute of Integrative Medicine(IN)
Publications by Year
Research Areas
Catalytic C–H Functionalization Methods, Catalytic Cross-Coupling Reactions, Cancer-related Molecular Pathways, Crystallization and Solubility Studies, X-ray Diffraction in Crystallography
Most-Cited Works
- → Cross-Dehydrogenative Coupling of Azoles with α-C(sp3)–H of Ethers and Thioethers under Metal-Free Conditions: Functionalization of H–N Azoles via C–H Activation(2015)82 cited
- → Design of Novel 3-Pyrimidinylazaindole CDK2/9 Inhibitors with Potent In Vitro and In Vivo Antitumor Efficacy in a Triple-Negative Breast Cancer Model(2017)64 cited
- → Iron oxide mediated direct C–H arylation/alkylation at α-position of cyclic aliphatic ethers(2011)58 cited
- → Metal-free Cross-Dehydrogenative Coupling of HN-azoles with α-C(sp3)-H Amides via C–H Activation and Its Mechanistic and Application Studies(2016)48 cited
- → I2/Aqueous TBHP-Catalyzed Coupling of Amides with Methylarenes/Aldehydes/Alcohols: Metal-Free Synthesis of Imides(2016)47 cited
- → New method for C–H arylation/alkylation at α-position of cyclic aliphatic ethers by iron-oxide mediated reaction(2012)45 cited
- → Metal free C–H functionalization of diazines and related heteroarenes with organoboron species and its application in the synthesis of a CDK inhibitor, meriolin 1(2016)22 cited
- → Small molecule ‘4ab’ induced autophagy and endoplasmic reticulum stress-mediated death of aggressive cancer cells grown under adherent and floating conditions(2023)16 cited
- → Newly synthesized 3-sulfenylindole derivatives from 4-hydroxydithiocoumarin using an oxidative cross dehydrogenative coupling reaction (OCDCR): potential lead molecules for antiproliferative activity(2020)12 cited
- → A Marine-based Meriolin (3-Pyrimidinylazaindole) Derivative (4ab) Targets PI3K/AKT /mTOR Pathway Inducing Cell Cycle Arrest and Apoptosis in Molt-4 Cells(2019)8 cited