Eshani Das

Affiliations: 
Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India 
Area:
Organic synthesis and theoretical chemistry
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"Eshani Das"
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Publications

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Roy B, Das E, Roy A, et al. (2020) Ni(ii)-Catalyzed vinylic C-H functionalization of 2-acetamido-3-arylacrylates to access isotetronic acids. Organic & Biomolecular Chemistry
Bhattacharya P, Singha M, Das E, et al. (2020) Pseudoasymmetry paradox: A suggestion to introduce the term pseudostereogenicity and address reflection issues Tetrahedron. 76: 131244
Das E, Basak A. (2019) Regioselective Synthesis of Benzo-fused Tetrahydroisoquinoline-based Biaryls through a Tandem One-pot Halogenation of p-Benzynes from Enediynes and Suzuki-Miyaura Coupling. The Journal of Organic Chemistry
Das E, Basak S, Anoop A, et al. (2019) How to achieve high regioselectivity in barrier-less nucleophilic addition to p-benzynes generated via Bergman Cyclization of unsymmetrical cyclic azaenediyne? The Journal of Organic Chemistry
Das E, Basak S, Anoop A, et al. (2018) An Experiment cum Computational Study on the Regioselectivity of Nucleophilic Addition to Unsymmetrical p-Benzynes Derived from Bergman Cyclization of Enediynes. The Journal of Organic Chemistry
Bhattacharya P, Singha M, Das E, et al. (2018) Recent advances in Garratt-Braverman cyclization: Mechanistic and synthetic explorations Tetrahedron Letters. 59: 3033-3051
Panja A, Das E, Maji M, et al. (2016) ChemInform Abstract: Synthesis of Phthalides from Bis-propargyl Ethers: Use of Garratt-Braverman Cyclization to Construct the Phthalans and IBX as a New Reagent for Subsequent Oxidation. Cheminform. 47: no-no
Das J, Das E, Jana S, et al. (2015) Shifting the Reactivity of Bis-propargyl ethers from Garratt-Braverman Cyclization Mode to 1, 5- H shift Pathway to Yield 3, 4-Disubstituted Furans: A Combined Experimental and Computational Study. The Journal of Organic Chemistry
Panja A, Das E, Maji M, et al. (2015) Synthesis of phthalides from bis-propargyl ethers: Use of Garratt-Braverman cyclization to construct the phthalans and IBX as a new reagent for subsequent oxidation Tetrahedron Letters. 56: 5986-5990
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