Sunay V. Chankeshwara - Publications

Affiliations: 
University of Edinburgh, Edinburgh, Scotland, United Kingdom 
 2008 National Institute of Pharmaceutical Education and Research, Mohali 

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
2009 Chakraborti AK, Singh B, Chankeshwara SV, Patel AR. Protic acid immobilized on solid support as an extremely efficient recyclable catalyst system for a direct and atom economical esterification of carboxylic acids with alcohols. The Journal of Organic Chemistry. 74: 5967-74. PMID 19618958 DOI: 10.1021/Jo900614S  0.607
2009 Chakraborti AK, Chankeshwara SV. Counterattack mode differential acetylative deprotection of phenylmethyl ethers: applications to solid phase organic reactions. The Journal of Organic Chemistry. 74: 1367-70. PMID 19117380 DOI: 10.1021/Jo801659G  0.526
2008 Chankeshwara SV, Chebolu R, Chakraborti AK. Organocatalytic methods for chemoselective O-tert-butoxycarbonylation of phenols and their regeneration from the O-t-Boc derivatives. The Journal of Organic Chemistry. 73: 8615-8. PMID 18844417 DOI: 10.1021/Jo8013325  0.717
2008 Chakraborti A, Chebolu R, Chankeshwara S. Triphenylphosphine as a Novel Organocatalyst for Chemoselective O-tert-Butoxycarbonylation of Phenols Synthesis. 2008: 1448-1454. DOI: 10.1055/S-2008-1072565  0.716
2008 Chankeshwara S. Dimethyl Carbonate (DMC): A Versatile and Environmentally Benign Building Block Synlett. 2008: 624-625. DOI: 10.1055/S-2008-1032048  0.454
2008 Chebolu R, Chankeshwara SV, Chakraborti AK. ChemInform Abstract: Triphenylphosphine as a Novel Organocatalyst for Chemoselective O-tert-Butoxycarbonylation of Phenols. Cheminform. 39. DOI: 10.1002/CHIN.200837053  0.725
2008 Chakraborti AK, Rudrawar S, Jadhav KB, Kaur G, Chankeshwara SV. ChemInform Abstract: “On Water” Organic Synthesis: A Highly Efficient and Clean Synthesis of 2-Aryl/Heteroaryl/Styryl Benzothiazoles and 2-Alkyl/Aryl Alkyl Benzothiazolines. Cheminform. 39. DOI: 10.1002/CHIN.200815129  0.544
2007 Chakraborti AK, Rudrawar S, Jadhav KB, Kaur G, Chankeshwara SV. “On water” organic synthesis: a highly efficient and clean synthesis of 2-aryl/heteroaryl/styryl benzothiazoles and 2-alkyl/aryl alkyl benzothiazolines Green Chemistry. 9: 1335. DOI: 10.1039/B710414F  0.722
2006 Chankeshwara SV, Chakraborti AK. Catalyst-free chemoselective N-tert-butyloxycarbonylation of amines in water. Organic Letters. 8: 3259-62. PMID 16836380 DOI: 10.1021/Ol0611191  0.596
2006 Chakraborti AK, Chankeshwara SV. HClO4-SiO2 as a new, highly efficient, inexpensive and reusable catalyst for N-tert-butoxycarbonylation of amines. Organic & Biomolecular Chemistry. 4: 2769-71. PMID 16826301 DOI: 10.1039/B605074C  0.59
2006 Chankeshwara SV, Chakraborti AK. Indium(III) Halides as New and Highly Efficient Catalysts for N-tert-Butoxycarbonylation of Amines. Cheminform. 37. DOI: 10.1055/S-2006-942492  0.628
2006 Chakraborti A, Chankeshwara S. Indium(III) Halides as New and Highly Efficient Catalysts for N-tert-Butoxycarbonylation of Amines Synthesis. 2006: 2784-2788. DOI: 10.1055/S-2006-942492  0.536
2006 Chankeshwara SV, Chakraborti AK. Copper(II) tetrafluoroborate as a novel and highly efficient catalyst for N-tert-butoxycarbonylation of amines under solvent-free conditions at room temperature Tetrahedron Letters. 47: 1087-1091. DOI: 10.1016/J.Tetlet.2005.12.044  0.611
2006 Chankeshwara SV, Chakraborti AK. Montmorillonite K 10 and montmorillonite KSF as new and reusable catalysts for conversion of amines to N-tert-butylcarbamates Journal of Molecular Catalysis a: Chemical. 253: 198-202. DOI: 10.1016/J.Molcata.2006.03.042  0.612
2006 Chankeshwara SV, Chakraborti AK. Copper(II) Tetrafluoroborate as a Novel and Highly Efficient Catalyst for N-tert-Butoxycarbonylation of Amines under Solvent-Free Conditions at Room Temperature. Cheminform. 37. DOI: 10.1002/CHIN.200621075  0.529
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