Academic
Exam | Institution | Year | Specialization | Division |
---|---|---|---|---|
B.Sc | Dibrugarh University | 2010 | Chemistry | 1st |
M.Sc | Tezpur University | 2012 | Chemistry | 1st |
Ph.D | Tezpur University | 2017 | Organic synthesis, Catalysis | --- |
Awards
- Borah, R., Dutta, A. K., Sarma, P., Dutta, C., & Sarma, B. (2014). Synthesis of anti-2, 3- dihydro-1, 2, 3-trisubstituted-1 H-naphth [1, 2-e][1, 3] oxazine
- Dutta, A. K., Gogoi, P., & Borah, R. (2014). Synthesis of dibenzoxanthene and acridine derivatives catalyzed by 1, 3-disulfonic acid imidazolium carboxylate ionic liquids. RSC advances, 4(78), 41287-41291
- Dutta, P., Dutta, A. K., Sarma, P., & Borah, R. (2014). Dual nature of polyethylene glycol under microwave irradiation for the clean synthesis of oximes. Monatshefte für Chemie Chemical Monthly, 145(3), 505-508
- Sarma, P., Dutta, A. K., Gogoi, P., Sarma, B., & Borah, R. (2015). 3-Methyl-1- sulfoimidazolium ionic liquids as recyclable medium for efficient synthesis of quinoline derivatives by Friedländer annulation. Monatshefte für Chemie-Chemical Monthly, 146(1), 173-180.
- Gogoi, P., Dutta, A. K., Sarma, P., & Borah, R. (2015). Development of Brönsted–Lewis acidic solid catalytic system of 3-methyl-1-sulfonic acid imidazolium transition metal chlorides for the preparation of bis (indolyl) methanes. Applied Catalysis A: General, 492, 133-139.
- Dutta, A. K., Gogoi, P., Saikia, M. P., & Borah, R. (2016). Development of environmentally benign methods towards the synthesis of anti-2, 3-dihydro-1, 2, 3- trisubstituted-1H-naphth [1, 2-e][1, 3] oxazines using brønsted acidic catalysts. Catalysis Letters, 146(5), 902-908
- Saikia, S., Gogoi, P., Dutta, A. K., Sarma, P., & Borah, R. (2016). Design of multifaceted acidic 1, 3-disulfoimidazolium chlorometallate ionic systems as heterogeneous catalysts for the preparation of β-amino carbonyl compounds. Journal of Molecular Catalysis A: Chemical, 416, 63-72
- Gogoi, P., Dutta, A. K., Saikia, S., & Borah, R. (2016). Heterogenized hybrid catalyst of 1-sulfonic acid-3-methyl imidazolium ferric chloride over NaY zeolite for one-pot synthesis of 2-amino-4-arylpyrimidine derivatives: A viable approach. Applied Catalysis A: General, 523, 321-331
- Dutta, A. K., Gogoi, P., Saikia, S., & Borah, R. (2017). N, N-disulfo-1, 1, 3, 3- tetramethylguanidinium carboxylate ionic liquids as reusable homogeneous catalysts for multicomponent synthesis of tetrahydrobenzo [a] xanthene and tetrahydrobenzo [a] acridine derivatives. Journal of Molecular Liquids, 225, 585-591
- Sarma, P., Dutta, A. K., & Borah, R. (2017). Design and exploration of–SO3H group functionalized Brønsted acidic ionic liquids (BAILs) as task-specific catalytic systems for organic reactions: a review of literature. Catalysis Surveys from Asia, 21(2), 70-93
- Dutta, A. K., Gogoi, P., & Borah, R. (2017). Triphenylsulfophosphonium chlorometallates as efficient heterogeneous catalysts for the three-component synthesis of 2, 3-dihydro-1, 2, 3-trisubstituted-1H-naphth [1, 2-e][1, 3] oxazines. Polyhedron, 123, 184-191.
- Gogoi, P., Dutta, A. K., & Borah, R. (2017). Studies on Structural Changes and Catalytic Activity of Y-zeolite Composites of 1, 3-disulfoimidazolium trifluoroacetate Ionic Liquid (IL) for Three Component Synthesis of 3, 4-dihydropyrimidinones. Catalysis Letters, 147(3), 674-685
- Dutta, A. K., Gogoi, P., & Borah, R. (2018). Diethyldisulfoammonium chlorometallates as heterogeneous Brønsted–Lewis acidic catalysts for one‐pot synthesis of 14‐aryl‐7‐(N‐ phenyl)‐14H‐dibenzo [a, j] acridines. Applied Organometallic Chemistry, 32(1), e3900
- Gogoi, P., Saikia, S., Dutta, A. K., & Borah, R. (2018). Acidic and Basic Functionalized Ionic Liquid Systems for Advanced Synthesis of Five and Six Membered Nitrogenates Heterocycles. In Advances in Organic Synthesis (Vol. 10, pp. 139-196). Bentham Publisher United Arab Emirates. (BOOK CHAPTER)
- Dutta, A. K., Boruah, K., & Borah, R. (2021). Development of N, N-disulfo-1, 1, 3, 3- tetramethylguanidinium chlorometallates as heterogeneous catalysts for one pot synthesis of 1, 2-dihydro-1-aryl-3H-naphth [1, 2-e][1, 3] oxazin-3-one derivatives. Current Organocatalysis, 8(2), 172-186