Arindam Maity
Affiliations: | 2016-2021 | IISER Bhopal |
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Maity A, Roy A, Das MK, et al. (2020) Oxidative cyanation of 2-oxindoles: formal total synthesis of (±)-gliocladin C. Organic & Biomolecular Chemistry |
Roy A, Maity A, MK SS, et al. (2020) Hexahydropyrrolo-[2,3-b]-indole alkaloids of biological relevance: proposed biosynthesis and synthetic approaches Arkivoc. 2020: 437-471 |
Roy A, Maity A, Giri R, et al. (2020) Efficient Alkynylation of 2‐Oxindoles with Alkynyl Dibenzothiophenium Triflates: Total Synthesis of (±)‐Deoxyeseroline Asian Journal of Organic Chemistry. 9: 226-232 |
Kumar N, Maity A, Gavit VR, et al. (2018) A catalytic N-deacylative alkylation approach to hexahydropyrrolo[2,3-b]indole alkaloids. Chemical Communications (Cambridge, England) |
Kumar N, Gavit VR, Maity A, et al. (2018) Pd(0)-Catalyzed Chemoselective Deacylative Alkylations (DaA) of N-Acyl-2-oxindoles: Total Syntheses of Pyrrolidino[2,3-b]indoline Alkaloids, (±)-Deoxyeseroline and (±)-Esermethole. The Journal of Organic Chemistry |
Mondal S, Maity A, Paira R, et al. (2013) ChemInform Abstract: Efficient Synthesis of Novel Tetrahydropyrrolo[3′,4′:3,4]pyrrolo[2,1-a]isoquinoline Derivatives via a Simple and Convenient MCR in Aqueous Micellar System. Cheminform. 44: no-no |
Mondal S, Maity A, Paira R, et al. (2012) Efficient synthesis of novel tetrahydropyrrolo[3′,4′:3,4]pyrrolo[2,1-a] isoquinoline derivatives via a simple and convenient MCR in aqueous micellar system Tetrahedron Letters. 53: 6288-6291 |
Paira R, Sahu KB, Mondal S, et al. (2012) ChemInform Abstract: Effective Suzuki-Miyaura Arylation and Sonogashira Aryl Alkynylation on N-Heteroaromatic Cations: Synthesis of Substituted Pyridine-Fused Cationic Heterocycles. Cheminform. 43: no-no |
Mondal N, Paira R, Sahu K, et al. (2011) Effective Suzuki-Miyaura Arylation and Sonogashira Aryl Alkynylation on N-Heteroaromatic Cations: Synthesis of Substituted Pyridine-Fused Cationic Heterocycles Synthesis. 2011: 3006-3014 |
Mondal N, Mondal S, Maity A, et al. (2011) Facile Synthesis of Tricyclic Oxazino- or Oxazepino-Fused Tetrahydroquinolines via Intramolecular Reductive Amidation Synthesis. 2011: 2079-2084 |