Radhakrishna Gattu
Affiliations: | IIT Guwahati |
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Parents
Sign in to add mentorAbu Taleb Khan | grad student | 2018 | IIT Guwahati | |
(Exploration of Amines for the Synthesis of Substituted Quinolines and Indoles) |
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Publications
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Ali S, Gattu R, Singh V, et al. (2020) Reaction behaviour of arylamines with nitroalkenes in the presence of bismuth(iii) triflate: an easy access to 2,3-dialkylquinolines. Organic & Biomolecular Chemistry |
Gattu R, Mondal S, Ali S, et al. (2018) Iodine monobromide catalysed regioselective synthesis of 3-arylquinolines from α-aminoacetophenones and trans-β-nitrostyrenes. Organic & Biomolecular Chemistry |
Gattu R, Bhattacharjee S, Mahato K, et al. (2018) Electronic effect of substituents on anilines favors 1,4-addition to trans-β-nitrostyrenes: access to N-substituted 3-arylindoles and 3-arylindoles. Organic & Biomolecular Chemistry |
Mahato K, Arora N, Ray Bagdi P, et al. (2018) An oxidative cross-coupling reaction of 4-hydroxydithiocoumarin and amines/thiols using a combination of I2 and TBHP: access to lead molecules for biomedical applications. Chemical Communications (Cambridge, England) |
Ghosh A, Gattu R, Khan AT. (2018) Synthesis of Benzothiazoles via Condensation Reaction of 2-Aminothiophenols and β -Oxodithioesters Using a Combination of PTSA and CuI as Catalyst Chemistryselect. 3: 13773-13776 |
Bhattacharjee S, Gattu R, Khan AT. (2018) Triethylamine-Mediated One-Pot Synthesis of Benzo[f]chromene Derivatives Chemistryselect. 3: 4760-4763 |
Gattu R, Bagdi PR, Basha RS, et al. (2017) Camphorsulfonic Acid Catalysed One-Pot Three Component Reaction for the Synthesis of Fused Quinoline and Benzoquinoline Derivatives. The Journal of Organic Chemistry |
Gattu R, Basha RS, Bagdi PR, et al. (2016) One-pot three-component regioselective synthesis of C1-functionalised 3-arylbenzo[f]quinoline Rsc Advances. 6: 11675-11682 |
Gattu R, Basha RS, Bagdi PR, et al. (2016) ChemInform Abstract: One-Pot Three-Component Regioselective Synthesis of C1-Functionalized 3-Arylbenzo[f]quinoline. Cheminform. 47 |