Search Results - "Reddy, K. Harsha Vardhan"
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Magnetically Separable CuFe2O4 Nanoparticle Catalyzed C–Se Cross Coupling in Reusable PEG Medium
Published in Chemistry letters (05-06-2012)“…A simple and efficient procedure for the synthesis of unsymmetrical diaryl selenides has been developed by magnetically separable CuFe2O4 nanoparticle…”
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Nano copper oxide catalyzed synthesis of symmetrical diaryl sulfides under ligand free conditions
Published in Beilstein journal of organic chemistry (30-06-2011)“…Potassium thiocyanate acts as an efficient sulfur surrogate in C-S cross-coupling reactions mediated by recyclable copper oxide nanoparticles under ligand free…”
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A mild and expeditious synthesis of amides from aldehydes using bio glycerol-based carbon as a recyclable catalyst
Published in Tetrahedron letters (23-05-2012)“…The new bioglycerol-based carbon catalyst acts as an efficient, readily available, and reusable catalyst for the synthesis of amides, when aldehyde and…”
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Synthesis of Biheterocycles Based on Quinolinone, Chromone, and Coumarin Scaffolds by Palladium-Catalyzed Decarboxylative Couplings
Published in Journal of organic chemistry (15-01-2016)“…An efficient Pd-catalyzed decarboxylative coupling of heterocyclic carboxylic acids with heterocyclic halides to achieve the synthesis of biheterocycles of…”
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Convergent Strategy to Dizocilpine MK-801 and Derivatives
Published in Journal of organic chemistry (06-04-2018)“…A convergent total synthesis of MK-801 has been achieved. Key synthetic transformations include a multicomponent Barbier-type reaction to construct the…”
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Conversion of 3‑Bromo‑2H‑coumarins to 3‑(Benzofuran-2-yl)‑2H‑coumarins under Palladium Catalysis: Synthesis and Photophysical Properties Study
Published in Organic letters (17-02-2017)“…An intriguing conversion of 3-bromo-2H-coumarins to 3-(benzofuran-2-yl)-2H-coumarins under palladium catalysis is reported. The process involves, from only one…”
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Productive Syntheses of Privileged Scaffolds Inspired by the Recognition of a Diels–Alder Pattern Common to Three Classes of Natural Products
Published in Chemistry : a European journal (01-12-2020)“…Identification of a common Diels–Alder pattern in three classes of bioactive natural products led us to study the synthesis and cycloaddition of a new class of…”
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Quinoxaline synthesis in novel tandem one-pot protocol
Published in Tetrahedron letters (01-06-2011)“…A variety of quinoxalines were synthesized via tandem one-pot procedure for the first time in water medium. The key strategy was the in situ preparation of…”
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Recent Developments in the Synthesis of Quinoxaline Derivatives by Green Synthetic Approaches
Published in Organic preparations and procedures international (01-01-2013)“…Organic Preparations and Procedures International Recent Developments in the Synthesis of Quinoxaline Derivatives by Green Synthetic Approaches…”
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A novel one-pot synthesis of spiro[indoline-3,4′-pyrazolo[3,4-e][1,4]thiazepine] diones using recyclable bioglycerol-based sulfonic acid functionalized carbon catalyst
Published in Tetrahedron letters (04-07-2012)“…A novel, simple, and efficient synthetic protocol has been developed for the synthesis of spiro[indoline-3,4′-pyrazolo[3,4-e][1,4]thiazepine] diones, by using…”
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Magnetically separable CuFe2O4 nano particles catalyzed multicomponent synthesis of 1,4-disubstituted 1,2,3-triazoles in tap water using ‘click chemistry’
Published in Tetrahedron letters (22-08-2012)“…The synthesis of 1,4-disubstituted 1,2,3-triazoles is attempted using magnetically separable and reusable copper ferrite nano particles in a one pot reaction,…”
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Efficient and Direct Synthesis of γ‐Amino‐α,β‐Unsaturated Amides by Catalyzed Allylic Substitution of α‐Fluoroenamides: Toward to Synthesis of Hybrid Peptides and Indolizidines
Published in European journal of organic chemistry (29-03-2018)“…A variety of γ‐amino‐α,β‐unsaturated amides have been synthesized from readily available α‐fluoroenamides precursors via an unprecedented intermolecular and…”
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Copper on chitosan: an efficient and easily recoverable heterogeneous catalyst for one pot synthesis of 1,2,3-triazoles from aryl boronic acids in water at room temperature
Published in Tetrahedron letters (08-04-2015)“…[Display omitted] A facile, efficient, and environmentally-friendly one pot protocol has been developed for the synthesis of 1,4-diaryl-1,2,3-triazoles from…”
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A mild method for the replacement of a hydroxyl group by halogen: 2. unified procedure and stereochemical studies
Published in Tetrahedron (11-09-2020)“…N,N-Dimethyl- and N,N-diisopropyl-1-halo-2-methyl-l-propenylamines are readily available reagents for the mild deoxyhalogenation of alcohols and hydroxyacids…”
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Tandem supramolecular synthesis of substituted 2-aryl-2,3-dihydroquinazolin-4(1H)-ones in the presence of β-cyclodextrin in water
Published in Tetrahedron letters (07-11-2012)“…Substituted 2-aryl-2,3-dihydroquinazolin-4(1H)-ones were prepared for the first time in water under neutral conditions by the reaction of aniline, isatoic…”
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Copper oxide nanoparticles catalyzed synthesis of aryl sulfides via cascade reaction of aryl halides with thiourea
Published in Tetrahedron letters (25-05-2011)“…Recyclable copper oxide nanoparticles catalyzed simple and highly efficient protocol for the synthesis of symmetrical aryl sulfides was developed by the…”
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Metal free synthesis of diaryl selenides using SeO 2 as a selenium source
Published in Tetrahedron letters (01-09-2016)Get full text
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Metal free synthesis of diaryl selenides using SeO2 as a selenium source
Published in Tetrahedron letters (14-09-2016)“…[Display omitted] •High functional group compatibility.•High yields.•Avoiding harmful organic solvents.•This protocol may be useful for basic as well as…”
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An efficient synthesis of N-substituted indoles from indoline/indoline carboxylic acid via aromatization followed by C–N cross-coupling reaction by using nano copper oxide as a recyclable catalyst
Published in Tetrahedron letters (13-06-2012)“…A new and elegant protocol for the synthesis of 1-substituted indoles was developed via aromatization of indoline/indoline carboxylic acid followed by C–N…”
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