Amrita Chakraborty
Affiliations: | 2009-2014 | Jadavpur | IACS Kolkata |
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| Chakraborty A, Jana S, Kibriya G, et al. (2016) ChemInform Abstract: tert-Butyl Nitrite Mediated Azo Coupling Between Anilines and Imidazoheterocycles. Cheminform. 47 |
| Chakraborty A, Jyothi K, Sinha S. (2015) ChemInform Abstract: Palladium-Catalyzed Synthesis of 2-Allylindole and 2-Allylbenzofuran Derivatives from 2-((Trimethylsilyl)ethynyl)arenes. Cheminform. 46: no-no |
| Mitra S, Chakraborty A, Mishra S, et al. (2014) Copper(I)-catalyzed oxidative coupling between 2-aminobenzothiazole and terminal alkyne: formation of benzothiazine. Organic Letters. 16: 5652-5 |
| Chakraborty A, Jyothi K, Sinha S. (2014) Palladium-catalyzed synthesis of 2-allylindole and 2-allylbenzofuran derivatives from 2-((trimethylsilyl)ethynyl)arenes Tetrahedron Letters. 55: 6795-6798 |
| Chakraborty A, Goswami K, Adiyala A, et al. (2014) ChemInform Abstract: Syntheses of Spiro[cyclopent[3]ene-1,3′-indoles]s and Tetrahydrocyclohepta[b]indoles from 2,3-Disubstituted Indoles Through Sigmatropic Rearrangement. Cheminform. 45: no-no |
| Rakshit S, Saha R, Chakraborty A, et al. (2013) Effect of hydrophobic interaction on structure, dynamics, and reactivity of water. Langmuir : the Acs Journal of Surfaces and Colloids. 29: 1808-17 |
| Chakraborty A, Goswami K, Adiyala A, et al. (2013) Syntheses of Spiro[cyclopent[3]ene-1,3′-indole]s and Tetrahydrocyclohepta[b]indoles from 2,3-Disubstituted Indoles through Sigmatropic Rearrangement European Journal of Organic Chemistry. 2013: 7117-7127 |
| Goswami K, Chakraborty A, Sinha S. (2013) Synthesis of Optically Active Selenium-Containing Isotryptophan, Homoisotryptophan, and Homotryptophan European Journal of Organic Chemistry. 2013: 3645-3647 |
| Chakraborty A, Sinha S. (2012) ChemInform Abstract: Synthesis of 3-[2-(1,3-Butadienyl)]-1H-indoles en route to Murrapanine Analogue. Cheminform. 43: no-no |
| Chakraborty A, Sinha S. (2011) Synthesis of 3-[2-(1,3-butadienyl)]-1H-indoles en route to murrapanine analogue Tetrahedron Letters. 52: 6635-6638 |