G
Gal Reddy
Arizona State University, Aragen Life Sciences Pvt Ltd, Indian Institute of Chemical Technology
0000-0002-1390-9526
About
Gal Reddy Potuganti is a postdoctoral researcher at the University of Oklahoma, USA. He obtained his Ph.D. in Organic Chemistry from CSIR–Indian Institute of Chemical Technology (CSIR-IICT), Hyderabad, India, in 2021. His research focuses on the design and synthesis of cyclic nucleotide monophosphates (cNMPs), with expertise in multicomponent reactions and spiro heterocyclic chemistry. He previously worked at Arizona State University and Aragen Life Sciences Pvt. Ltd..
Employment
-
Arizona State University Post-Doctoral Researcher2022 - 2025
-
Aragen Life Sciences Pvt Ltd Associate Scientist2020 - 2021
-
Indian Institute of Chemical Technology2015 - 2020
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (15)
- Copper‐Catalyzed Sequential Azide‐Alkyne Cycloaddition (CuAAc) and Ullmann Coupling: A Tandem One‐Pot Synthesis of Quinazolino[3,2‐c][1,2,3] Triazolo[1,5‐a]‐Quinazolin‐14‐One Save
- Front Cover: Copper‐Catalyzed Sequential Azide‐Alkyne Cycloaddition (CuAAc) and Ullmann Coupling: A Tandem One‐Pot Synthesis of Quinazolino[3,2‐c][1,2,3] Triazolo[1,5‐a]‐Quinazolin‐14‐One (Eur. J. Org. Chem. 15/2026) Save
- Fluorine-containing FDA-approved small-molecule drugs in 2025: significance, synthetic insights, and therapeutic applications Save
- Nitrogen-containing FDA-approved drugs in 2025: synthesis, significance and therapeutic applications Save
- Site-Selective Tyrosine Phosphorylation in the Activation of the p50 Subunit of NF-κB for DNA Binding and Transcription Save
- Copper Mediated Direct Amination: Synthesis of 1,2,3,15 a-tetrahydro-14H-pyrrolo[1,2-a]quinazolino[3,2-c]quinazolin-14-onederivatives via 2-(2-bromophenyl)quinazolin-4(3H)-ones Save
- Multicomponent Domino Approaches for the Synthesis of Spirooxazolidine‐2‐thiones and Spirooxothiolane‐2‐imines Save
- Synthesis of dihydropyrrole derivatives by oxidative functionalization of 2-Amino-4H-chromenes using hypervalent Iodine reagents Save
- Exo-selective intermolecular Diels–Alder reaction by PyrI4 and AbnU on non-natural substrates Save
- CuI/I2‐Catalyzed Concise Synthesis of Substituted 6‐Aminoisoquinolinoquinazoline Carboxylates from Anthranilamide Save