E. A. Jaseer - Publications

Affiliations: 
2010 IIT Madras 

15 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 Barman S, Garcia N, Jaseer EA, Elanany M, Khawaji M, Alasiri H, Peedikakkal AMP, Akhtar MN, Theravalappil R. Unveiling -Alkyloxy/-Silyloxy-Substituted -Aryl PNP Ligands for Efficient Cr-Catalyzed Ethylene Tetramerization. Acs Omega. 8: 26437-26443. PMID 37521606 DOI: 10.1021/acsomega.3c03029  0.338
2016 Iturmendi A, García N, Jaseer EA, Munárriz J, Sanz Miguel PJ, Polo V, Iglesias M, Oro LA. N-Heterocyclic olefins as ancillary ligands in catalysis: a study of their behaviour in transfer hydrogenation reactions. Dalton Transactions (Cambridge, England : 2003). PMID 27472896 DOI: 10.1039/C6Dt02571D  0.367
2016 Rubio-Pérez L, Jaseer EA, García N, Polo V, Iglesias M, Oro LA. Experimental and Computational Studies on the Reactivity and Binding Mode of Thiophene with N-Heterocyclic Carbene Iridium Complexes Organometallics. 35: 569-578. DOI: 10.1021/Acs.Organomet.5B00995  0.306
2016 Julian A, Polo V, Jaseer EA, Fernandez-Alvarez FJ, Oro LA. ChemInform Abstract: Solvent-Free Iridium-Catalyzed Reactivity of CO2with Secondary Amines and Hydrosilanes. Cheminform. 47: no-no. DOI: 10.1002/CHIN.201615071  0.311
2015 Julián A, Polo V, Jaseer EA, Fernández-Alvarez FJ, Oro LA. Solvent-Free Iridium-Catalyzed Reactivity of CO2 with Secondary Amines and Hydrosilanes Chemcatchem. 7: 3895-3902. DOI: 10.1002/Cctc.201500651  0.414
2010 Jaseer E, Karthikeyan I, Sekar G. Halogenative kinetic resolution of β-aryloxy cyclic alcohols: chiral BINAP-mediated SN2 displacement of hydroxy groups by chlorides with inversion of stereochemistry Tetrahedron: Asymmetry. 21: 2177-2182. DOI: 10.1016/J.TETASY.2010.06.034  0.338
2010 Jaseer E, Prasad D, Sekar G. Domino synthesis of 2-arylbenzo[b]furans by copper(II)-catalyzed coupling of o-iodophenols and aryl acetylenes Tetrahedron. 66: 2077-2082. DOI: 10.1016/J.TET.2010.01.026  0.321
2010 Jaseer EA, Prasad DJC, Dandapat A, Sekar G. ChemInform Abstract: An Efficient Copper(II)-Catalyzed Synthesis of Benzothiazoles Through Intramolecular Coupling-Cyclization of N-(2-Chlorophenyl)benzothioamides. Cheminform. 42: no-no. DOI: 10.1002/CHIN.201102149  0.3
2010 Jaseer EA, Sekar G. ChemInform Abstract: Halogenative Kinetic Resolution of β-Amido Alcohols: Chiral BINAP-Mediated SN2 Displacement of Hydroxy Groups by Chlorides with Inversion of Stereochemistry. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201046022  0.331
2010 Jaseer EA, Prasad DJC, Sekar G. ChemInform Abstract: Domino Synthesis of 2-Arylbenzo[b]furans by Copper(II)-Catalyzed Coupling of o-Iodophenols and Aryl Acetylenes. Cheminform. 41: no-no. DOI: 10.1002/CHIN.201027097  0.325
2009 Naidu AB, Jaseer EA, Sekar G. General, mild, and intermolecular Ullmann-type synthesis of diaryl and alkyl aryl ethers catalyzed by diol-copper(I) complex. The Journal of Organic Chemistry. 74: 3675-9. PMID 19361190 DOI: 10.1021/jo900438e  0.376
2009 Thakur K, Jaseer E, Naidu AB, Sekar G. An efficient copper(I) complex catalyzed Sonogashira type cross-coupling of aryl halides with terminal alkynes Tetrahedron Letters. 50: 2865-2869. DOI: 10.1016/J.TETLET.2009.03.146  0.329
2009 Rao RK, Naidu AB, Jaseer EA, Sekar G. ChemInform Abstract: An Efficient, Mild and Selective Ullmann-Type N-Arylation of Indoles Catalyzed by Copper(I) Complex. Cheminform. 40. DOI: 10.1002/CHIN.200939111  0.305
2009 Thakur KG, Jaseer EA, Naidu AB, Sekar G. ChemInform Abstract: An Efficient Copper(I) Complex Catalyzed Sonogashira-Type Cross-Coupling of Aryl Halides with Terminal Alkynes. Cheminform. 40. DOI: 10.1002/CHIN.200938091  0.336
2007 Jaseer EA, Naidu AB, Kumar SS, Rao RK, Thakur KG, Sekar G. Highly stereoselective chlorination of beta-substituted cyclic alcohols using PPh3-NCS: factors that control the stereoselectivity. Chemical Communications (Cambridge, England). 867-9. PMID 17308658 DOI: 10.1039/b614512d  0.358
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