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Subburethinam Ramesh, Ph.D - Publications

Affiliations: 
2009-2014 Chemistry University of Hyderabad, Hyderabad, Telangana, India 
 2014-2016 Chemistry University of Hyderabad, Hyderabad, Telangana, India 
 2017-2020 Chemistry DST Inspire faculty, SASTRA University, India 
Website:
https://www.sastra.edu/staffprofiles/schools/scbt.php?staff_id=R004
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32 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Perumal K, Lee J, Annes SB, Ramesh S, Rangarajan TM, Mathew B, Kim H. An efficient method to access spiro pseudoindoxyl ketones: evaluation of indoxyl and their -benzylated derivatives for inhibition of the activity of monoamine oxidases. Rsc Advances. 13: 24925-24935. PMID 37614797 DOI: 10.1039/d3ra03641c  0.74
2023 Annes SB, Perumal K, Anandhakumar K, Shankar B, Ramesh S. Transition-Metal-Free Dehydrogenation of Benzyl Alcohol for C-C and C-N Bond Formation for the Synthesis of Pyrazolo[3,4-]pyridine and Pyrazoline Derivatives. The Journal of Organic Chemistry. PMID 37125502 DOI: 10.1021/acs.joc.3c00382  0.796
2022 Saritha R, Annes SB, Perumal K, Shankar B, Ramesh S. Dimethyl Sulfoxide-Assisted, Iodine- and Ascorbic Acid-Catalyzed One-Pot Synthetic Approach for Constructing Highly Substituted Pyrazolo[1,5-]quinoline Thioether Derivatives. The Journal of Organic Chemistry. 87: 13856-13872. PMID 36215433 DOI: 10.1021/acs.joc.2c01557  0.792
2021 Saritha R, Annes SB, Ramesh S. Metal-free, regioselective, visible light activation of 4CzIPN for the arylation of 2-indazole derivatives. Rsc Advances. 11: 14079-14084. PMID 35423934 DOI: 10.1039/d1ra02372a  0.795
2021 Annes SB, Saritha R, Chandru K, Mandali PK, Ramesh S. Metal- and Solvent-Free Cascade Reaction for the Synthesis of Amino Pyrazole Thioether Derivatives. The Journal of Organic Chemistry. 86: 16473-16484. PMID 34747592 DOI: 10.1021/acs.joc.1c01846  0.79
2020 Saritha R, Annes SB, Subramanian S, Ramesh S. Correction: Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl-heteroaryl compounds. Organic & Biomolecular Chemistry. 18: 2962. PMID 32255143 DOI: 10.1039/d0ob90043e  0.758
2020 Saritha R, Annes SB, Saravanan S, Ramesh S. Carbazole based Electron Donor Acceptor (EDA) catalysis for the synthesis of biaryl and aryl-heteroaryl compounds. Organic & Biomolecular Chemistry. 18: 2510-2515. PMID 32195523 DOI: 10.1039/D0Ob00282H  0.78
2020 Annes SB, Saritha R, Subramanian S, Shankar B, Ramesh S. Solvent-free and montmorillonite K10-catalyzed domino reactions for the synthesis of pyrazoles with alkynylester as a dual synthon Green Chemistry. 22: 2388-2393. DOI: 10.1039/D0Gc00162G  0.811
2020 Subramaniyan SB, Annes SB, Yuvasri M, Nivedha K, Ramesh S, Anbazhagan V. 1,3,5‐Triphenylpyrazoline Based Fluorescent Probe for Selective Sensing and Imaging of Glutathione in Live Cell under Oxidative Stress Chemistryselect. 5: 515-521. DOI: 10.1002/slct.201904169  0.705
2019 Annes SB, Rajmohan R, Ramesh S, Vairaprakash P. Visible light mediated metal-free oxidative aromatization of 1,3,5-trisubstituted pyrazolines Tetrahedron Letters. 60: 150932. DOI: 10.1016/J.Tetlet.2019.07.023  0.759
2019 Annes SB, Vigneshwar K, Nivedha K, Manojveer S, Ramesh S. Deep Eutectic Solvent Mediated Alkyne‐Carbonyl Metathesis (ACM) Reaction for the Synthesis of 2H ‐Chromene Derivatives Chemistryselect. 4: 6245-6249. DOI: 10.1002/SLCT.201901350  0.803
2019 Annes SB, Ramesh S. 1,3,5‐Triphenylpyrazoline‐Based Organocatalysis: Synthesis of Aryl‐Heteroaryl Compounds and Exploiting By‐Product from the Reaction for Alkyne‐Carbonyl Metathesis (ACM) Reaction in One Pot Asian Journal of Organic Chemistry. 8: 1398-1404. DOI: 10.1002/Ajoc.201900305  0.822
2018 Annes SB, Vairaprakash P, Ramesh S. TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis. Rsc Advances. 8: 30071-30075. PMID 35546823 DOI: 10.1039/c8ra05702h  0.809
2018 Annes SB, Vairaprakash P, Ramesh S. TfOH mediated intermolecular electrocyclization for the synthesis of pyrazolines and its application in alkaloid synthesis Rsc Advances. 8: 30071-30075. DOI: 10.1039/C8Ra05702H  0.803
2016 Ramesh S, Nagarajan R. ChemInform Abstract: Copper-Catalyzed Hydroarylation of Alkynes for the Synthesis of Fascaplysin, Rutacarpine and Granulatimide Analogues. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201613130  0.35
2015 Ramesh S, Nagarajan R. Copper-catalyzed hydroarylation of alkynes for the synthesis of fascaplysin, rutacarpine and granulatimide analogues Synthesis (Germany). 47: 3573-3582. DOI: 10.1055/S-0034-1378735  0.445
2015 Ramesh S, Mehta G. A general, concise, 'collective' approach to eudesmanolide sesquiterpenoids: Total synthesis of bioactive atractylenolides I-IV and related natural products Tetrahedron Letters. 56: 5545-5548. DOI: 10.1016/J.Tetlet.2015.08.045  0.558
2015 Ramesh S, Mehta G. A total synthesis of sarcandralactone A: A general, concise, RCM enabled approach to lindenanolide sesquiterpenoids Tetrahedron Letters. 56: 3941-3944. DOI: 10.1016/J.Tetlet.2015.04.132  0.618
2015 Ramesh S, Nagarajan R. ChemInform Abstract: Copper Catalyzed Synthesis of Quinolinopyrano[2,3-b]carbazole Derivatives via Povarov Reaction. Cheminform. 46: no-no. DOI: 10.1002/CHIN.201505170  0.425
2014 Ramesh S, Nagarajan R. Copper catalyzed synthesis of quinolinopyrano[2,3-b]carbazole derivatives via Povarov reaction Journal of Chemical Sciences. 126: 1049-1054. DOI: 10.1007/S12039-014-0635-7  0.542
2013 Ramesh S, Kr Ghosh S, Nagarajan R. Copper catalyzed synthesis of fused benzimidazolopyrazine derivatives via tandem benzimidazole formation/annulation of δ-alkynyl aldehyde. Organic & Biomolecular Chemistry. 11: 7712-20. PMID 24108008 DOI: 10.1039/C3Ob41044G  0.677
2013 Ramesh S, Nagarajan R. A formal synthesis of lavendamycin methyl ester, nitramarine, and their analogues: a Povarov approach. The Journal of Organic Chemistry. 78: 545-58. PMID 23215629 DOI: 10.1021/Jo302389S  0.579
2013 Ramesh S, Nagarajan R. A novel route to synthesize lavendamycin analogues through an A3 coupling reaction Tetrahedron. 69: 4890-4898. DOI: 10.1016/J.Tet.2013.04.074  0.469
2013 Ramesh S, Nagarajan R. ChemInform Abstract: A Novel Route to Synthesize Lavendamycin Analogues Through an A3Coupling Reaction. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201343162  0.468
2012 Ramesh S, Nagarajan R. One-pot synthesis of pyrrolo[3,2-f]-and pyrrolo[2,3-h]quinoline derivatives: Observation of an unexpected mechanistic pathway Synlett. 23: 717-722. DOI: 10.1055/S-0031-1290565  0.417
2012 Ramesh S, Nagarajan R. ChemInform Abstract: Efficient One-Pot Multicomponent Synthesis of (Carbazolylamino)furan-2(5H)-one and Carbazolyltetrahydropyrimidine Derivatives Cheminform. 43: no-no. DOI: 10.1002/CHIN.201208142  0.345
2011 Ramesh S, Nagarajan R. Efficient one-pot multicomponent synthesis of (carbazolylamino)furan-2(5 H)-one and carbazolyltetrahydropyrimidine derivatives Synthesis. 3307-3317. DOI: 10.1055/S-0030-1260135  0.533
2011 Ramesh S, Nagarajan R. Synthesis of dihydrochromeno[4,3-b]pyrrolo[3,2-f]quinolines via intramolecular aza Diels-Alder reaction Tetrahedron Letters. 52: 4857-4860. DOI: 10.1016/J.Tetlet.2011.07.033  0.452
2011 Ramesh S, Nagarajan R. ChemInform Abstract: Synthesis of Dihydrochromeno[4,3-b]pyrrolo[3,2-f]quinolines via Intramolecular Aza Diels-Alder Reaction. Cheminform. 43: no-no. DOI: 10.1002/CHIN.201202147  0.356
2010 Ramesh S, Gaddam V, Nagarajan R. A flexible approach to the chromenoquinolines under copper/lewis acid catalysis Synlett. 757-760. DOI: 10.1055/S-0029-1219364  0.688
2010 Gaddam V, Ramesh S, Nagarajan R. CuI/La(OTf)3 catalyzed, one-pot synthesis of isomeric ellipticine derivatives in ionic liquid Tetrahedron. 66: 4218-4222. DOI: 10.1016/J.Tet.2010.03.095  0.756
2010 Gaddam V, Ramesh S, Nagarajan R. ChemInform Abstract: CuI/La(OTf)3Catalyzed, One-Pot Synthesis of Isomeric Ellipticine Derivatives in Ionic Liquid. Cheminform. 41. DOI: 10.1002/CHIN.201042149  0.325
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