​26. T. Ghosh,* Nickel-catalyzed regioselective access to dibenzo[c,f]oxocine framework via reductive Heck reaction, Synth. Commun. 2018, 48, 1338-1345.

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25. T. Ghosh,* M. Lehmann, Recent advances in heterocycle-based metal-free calamitics, J. Mater. Chem. C 2017, 5, 12308-12337.

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24. T. Ghosh*, Regioselective access of alkylidendibenzo[c,f]oxocine framework  via cyclocarbopalladation/cross-coupling cascade reactions and reductive Heck strategy, New J. Chem. 2017, 41, 2927-2933.

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23. S. Roy, S. Ponra, T. Ghosh, K. C. Majumdar, T. K. Das, Interaction of bovine serum albumin with synthetic spiropyrimidines, Adv. Mater. Lett. 2016, 7(1), 65-70.

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22. S. Roy, S. Ponra, T. Ghosh, R. Sadhukhan, K. C. Majumdar, T. K. Das,  Combined spectroscopic and molecular docking study of binding interaction of pyrano [3,2-f] quinoline derivatives with bovine serum albumins and its application in mammalian cell imaging, Adv. Mater. Lett. 2015, 6(11), 1004-1011.

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21. K. C. Majumdar, N. De, T. Ghosh, B. Roy, Iron-catalyzed synthesis of heterocycles, Tetrahedron 2014, 70, 4827-4868.

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20. K. C. Majumdar, S. Ponra, T. Ghosh, R. Sadhukha, U. Ghosh, Synthesis of novel pyrano[3,2-f]quinoline, phenanthroline derivatives and studies of their interactions with proteins: an application in mammalian cell imaging, Euro. J. Med. Chem. 2014, 71, 306-315.

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19. K. C. Majumdar, S. Ponra, T. Ghosh, Iron(III)chloride-catalyzed synthesis of functionalized spiropyrimidines, Synthesis 2013, 45, 3164-3172.

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18. K. C. Majumdar, T. Ghosh, S. Ponra, A reductive Mizoroki-Heck approach to dibenzo[b,e]oxepine, Tetrahedron Lett. 2013, 54, 4661-4665.

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17. K. C. Majumdar, T. Ghosh, D. S. S. Rao, S. K. Prasad, Unsymmetrical tetracatenar liquid crystals containing 2-phenylbenzoxazole: Synthesis and characterisation, Liq. Cryst. 2013, 40(3), 305-313.

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16. K. C. Majumdar, S. Ponra, T. Ghosh, Regioselective synthesis of pyrano[3,2-f]quinoline and phenanthroline derivatives using molecular iodine, Tetrahedron Lett. 2013, 54, 5586–5590.

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15. K. C. Majumdar, T. Ghosh, Synthesis and mesomorphic behavior of novel calamitic liquid crystalline dimesogens possessing a cholesteryl moiety connected to a pyrimidine core, Mol. Cryst. Liq. Cryst. 2013, 577, 15-24.

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14. K. C. Majumdar, S. Samanta, T. Ghosh, Synthesis of coumarin- and quinolone-annulated benzazocinone frameworks by a palladium-catalyzed intramolecular Heck reaction, Synthesis 2012, 44, 1711-1717.

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13. K. C. Majumdar, S. Ponra, T. Ghosh, Montmorillonite K-10 catalyzed, microwave-assisted cyclization of acetylinic amines: An efficient synthesis of pyrrolocoumarins and pyrroloquinolones, Synthesis 2012, 44, 2079-2083.

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12. K. C. Majumdar, S. Ponra, T. Ghosh, Green approach to highly functionalized thiopyrano derivatives via domino multi-component reaction in water, RSC Adv. 2012, 2, 1144-1152.

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11. K. C. Majumdar, T. Ghosh, D. S. S. Rao, S. K. Prasad, Unsymmetrical cholesterol and benzoxazole-based liquid crystalline dimers: synthesis and characterization, Liq. Cryst. 2011, 38(10), 1269-1277.

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10. K. C. Majumdar, T. Ghosh, P. K. Shyam, Facile regioselective synthesis of funtionalized heterocycle-tethered spiro-compounds via an intramolecular electrophilic ipso-iodocyclizaion process, Synlett 2011, 18, 2657-2662.

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9. K. C. Majumdar, T. Ghosh, D. S. S. Rao, S. K. Prasad, 2-phenylbenzoxazole-containing calamitic liquid crystals: synthesis and characterization, Liq. Cryst. 2011, 38(5), 625-632.

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8. K. C. Majumdar, T. Ghosh, P. K. Shyam, Ferrocene-based novel calamitic metallomesogens containing a 2-phenylbenzoxazole unit: synthesis and characterisation, Liq. Cryst. 2011, 38(5), 567-573.

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7. K. C. Majumdar, T. Ghosh, S. Samanta, Facile synthesis of coumarin- and quinolone-annulated benzazoninone derivatives by an intramolecular Heck reaction strategy via 9-exo-trig cyclization, Synthesis 2011, 10, 1569-1574.

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6. K. C. Majumdar, T. Ghosh, S. Chakravorty, N. Pal, D. S. S. Rao, S. K. Prasad, Cholesterol-based unsymmetrical Schiff’s base dimer terminated with 4-alkoxy-5-phenylthiophene unit: synthesis and characterisation,  Liq. Cryst. 2010, 37(12), 1539-1547.

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5. K. C. Majumdar, T. Ghosh, S. Chakravorty, Synthesis and characterization of symmetrical eight aromatic rings containing bent-shaped material derived from benzophenone, Mol. Cryst. Liq. Cryst. 2010, 533, 63-72. 

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4. K. C. Majumdar, S. Mondal, T. Ghosh, Synthesis and mesomorphic behavior of novel liquid-crystalline thiophene derivatives, Mol. Cryst. Liq. Cryst. 2010,  524, 17-25.

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3. K. C. Majumdar, T. Ghosh, S. Chakravorty, Palladium-mediated reductive Mizoroki–Heck cyclization strategy for the regioselective formation of dibenzoazocinone framework, Tetrahedron Lett. 2010, 51, 3372-3375.

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​2. K. C. Majumdar, K. Roy, S. Ganai, T. Ghosh, Catalyst-free 1,3-dipolar cycloaddition: An efficient route for the formation of the 1,2,3-triazole-fused diazepinone framework, Synthesis 2009, 5, 858-862.

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1. K. C. Majumdar, S. Chakravorty, T. Ghosh, B. Sridhar, Palladium-mediated reductive Heck cyclization for the formation of dibenzoazepinone framework, Synlett 2009, 19, 3127-3130.