Research output as part of PhD work

Synthesis of Poly-Functionalized Indolizines via [5+1] Annulative Access to Pyridines (Adv. syn. Cat., 2021, 363, 23, 5330-5335).
Regioselective Synthesis of 1-Cyano-3-arylindolizines: Construction of Pyrrole via DDQ-Mediated Ring Closure of Cyclopropyl Pyridines
Domino [4 + 2] Annulation Access to Quinone–Indolizine Hybrids: Anticancer N-Fused Polycycles (J. Org. Chem. 2020, 85, 16, 10994-1005).
Michael-Aldol-Double Elimination Cascade to Make Pyridines: Use of Chromone for the Synthesis of Indolizines (J. Org. Chem. 2021, 86, 15, 10235–10248). (Adv. Synth. Cat., 2022, July 25).
One-pot access to 2-amino-3-arylbenzofurans: direct entry to polyheterocyclic chemical space (Org. Biomol. Chem., 2020,18, 8119-8140).
Facile Access to 3, 4-Disubstituted 2H-Chromenes via Domino [4+ 2] Annulation (Synthesis 2021; 53(08): 1503-1512).
Solvent-Controlled Divergent Syntheses of Polycyclic N-Fused Heteroaromatics (Synthesis. 2020, 52(19):2841-56).
Benzofuro [2, 3-c] isoquinolines as novel AIEgens: Modulation of AIE characteristics by a single methoxy group. (Dyes and Pigments. 2022 Jul 21:110584).
Generation of a Poly-Functionalized Indolizine Scaffold and Its Anticancer Activity in Pancreatic Cancer Cells. (Bioorganic Chemistry. 2022; 126: 105877).
BF₃.OEt₂-Catalyzed One-pot Three-component Access to Diarymethylazides (Tetrahedron Letters. 2021, 67, 152820).

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