Y.V.D. Nageswar
Indian Institute of Chemical Technology
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Featured researches published by Y.V.D. Nageswar.
Canadian Journal of Chemistry | 2009
RegatiSridharR. Sridhar; BogaSrinivasB. Srinivas; BandaruMadhavB. Madhav; Vutukuri Prakash Reddy; Y.V.D. Nageswar; Kakulapati RamaRaoK.R. Rao
A neutral and efficient one-pot three-component aqueous-phase synthesis is developed for various spirooxindole derivatives from isatin, malononitrile, and 1,3-dicarbonyl compounds in high yields by...
RSC Advances | 2012
K. Harsha Vardhan Reddy; G. Satish; V. Prakash Reddy; B.S.P. Anil Kumar; Y.V.D. Nageswar
The recyclable Ru/C catalyzed oxidative α-cyanation of tertiary amines with ethyl cyanoformate by using TBHP as an oxidant under ambient conditions has been developed. Utilizing this protocol, α-aminonitrile derivatives were synthesized in good to excellent yields with high selectivity. The cyanide source (ethyl cyanoformate) employed herein was relatively cheap and less toxic, which would be beneficial. The catalyst was also inexpensive and commercially available as well as recyclable up to four cycles, without significant loss of its catalytic activity.
Organic Preparations and Procedures International | 2013
Y.V.D. Nageswar; K. Harsha Vardhan Reddy; K. Ramesh; S. Narayana Murthy
Introduction .....................................................................................2 I. Using Recyclable Catalysts................................................................3 A. Acid-catalyzed Reactions.......................................................................... 3 1. Sulfamic Acid-MeOH................................................................................ 3 2. Silica-supported Perchloric Acid................................................................ 4 3. Silica-bonded S-Sulfonic Acid ................................................................... 5 4. Iron-exchanged Molybdophosphoric Acid................................................... 5 B. Metal/metal Salt-catalyzed Reactions........................................................ 6 1. Ni-nano Particles ..................................................................................... 6 2. CuO Nano Particles.................................................................................. 7 3. Manganese Octahedral Molecular Sieves ................................................... 8 4. Silica-supported Antimony (III) Chloride.................................................... 8 5. ZnO-β Zeolite .......................................................................................... 9 6. PdCl2/Cu2Cl2 in PEG..............................................................................10 7. Ruthenium-on-charcoal ...........................................................................10 8. Zirconium (IV) Oxide Chloride Octahydrate ..............................................11 C. Other Recyclable Catalysts ......................................................................12 1. 1-(n-Butyl)imidazolium Tetrafluoroborate..................................................12 2. β-Cyclodextrin........................................................................................12 3. Hypervalent Iodine(III) Sulfonate-PEG 400...............................................13 4. Amberlyst-15 ..........................................................................................14 II. Using Microwave Energy ................................................................ 14 III. In Aqueous Media........................................................................... 19 1. Using Ceric(IV) Ammonium Nitrate ..........................................................19 2. Using Trimethylsilyl Chloride...................................................................20 3. Using N-Bromosuccinimide......................................................................21 IV. At Room Temperature .................................................................... 22 V. Conclusion...................................................................................... 25 References ...................................................................................... 25
Synthetic Communications | 2012
K. Ramesh; Sabbavarapu Narayana Murthy; Y.V.D. Nageswar
Abstract N-Substituted pyrroles were synthesized under neat conditions by the reaction of aromatic amines with 2, 5-dimethoxytetrahydrofuran in excellent yields. GRAPHICAL ABSTRACT
RSC Advances | 2014
B.S.P. Anil Kumar; K. Harsha Vardhan Reddy; G. Satish; R. Uday Kumar; Y.V.D. Nageswar
A novel one pot synthesis of β-hydroxy-1,4-disubstituted-1,2,3-triazoles has been developed by using CuFe2O4 magnetic nanoparticles. This methodology involves additive free, easily recyclable catalyst in water medium and avoids the handling of organic azides as they are generated in situ.
Synthetic Communications | 2007
V. Pavan Kumar; M. Narender; R. Sridhar; Y.V.D. Nageswar; K. Rama Rao
Abstract This is the first report on the supramolecular synthesis of thiazoles/aminothiazoles from β‐keto tosylates and thioamide/thiourea in water in the presence of β‐cyclodextrin in impressive yields. Formation of inclusion complexes was explained from 1H NMR studies.
Synthetic Communications | 2006
M. Somi Reddy; M. Narender; A. Mahesh; Y.V.D. Nageswar; K. Rama Rao
Abstract 1,3‐Oxathiolanes are smoothly deprotected to carbonyl compounds by IBX at room temperature with β‐cyclodextrin as a catalyst and water as solvent. IICT Communication No. 060424.
RSC Advances | 2014
K. Harsha Vardhan Reddy; B.S.P. Anil Kumar; V. Prakash Reddy; R. Uday Kumar; Y.V.D. Nageswar
A ligand free Ru/C-catalyzed amination of 2-halo azoles with a broad scope of aminating reagents has been developed. A variety of 2-aminoazole derivatives were synthesized in moderate to good yields by utilizing this protocol. The methodology is operationally simple and not sensitive to air and moisture. It provides potentially useful products by using an inexpensive and recyclable catalytic system under ligand free conditions without significant loss of its catalytic activity up to four cycles.
Synthetic Communications | 2012
K. Ramesh; B. Madhav; Sabbavarapu Narayana Murthy; Y.V.D. Nageswar
Abstract α-Hydroxyphosphonates were synthesized from aromatic/heteroaromatic aldehydes with triethyl phosphite in the presence of β-cyclodextrin in an aqueous medium. The β-cyclodextrin can be recovered and reused without loss of catalytic activity. GRAPHICAL ABSTRACT
Synthetic Communications | 2005
K. Surendra; N. Srilakshmi Krishnaveni; Y.V.D. Nageswar; K. Rama Rao
Abstract Several epoxides are efficiently converted to the corresponding β‐chlorohydrins in impressive yields with thionyl chloride in the presence of β‐cyclodextrin using water as solvent at room temperature.