Prakash P. Wadgaonkar
University of Tennessee
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Featured researches published by Prakash P. Wadgaonkar.
Synthetic Communications | 1990
George W. Kabalka; R. David Pace; Prakash P. Wadgaonkar
Abstract α, β-Unsaturated nitroalkenes are readily reduced to the corresponding oximes in good yields using ammonium formate in the presence of palladium. The reactions occur rapidly at room temperature in a solvent system of methanol and tetrahydrofuran.
Tetrahedron Letters | 2003
Susheel J. Nara; Jitendra R. Harjani; Manikrao M. Salunkhe; Ankush T. Mane; Prakash P. Wadgaonkar
1-Butyl-3-methylimidazolium hexafluorophosphate ionic liquid was employed as a reaction medium for lipase-catalysed aliphatic polyester synthesis. Lipase PS-C exhibited excellent catalysis in polycondensation of diethyl octane-1,8-dicarboxylate and 1,4-butanediol at room temperature and at 60°C. A relatively high molecular weight polymer was obtained at 60°C.
Synthetic Communications | 1990
George W. Kabalka; Prakash P. Wadgaonkar; Narayana Chatla
Abstract Borohydride supported on an ion exchange resin in methanol reduced aryl azides and arylsulfonyl azides to the corresponding aromatic amines and aryl sulfonamides in excellent yields. The isolation of pure products by simple filtration and evaporation is an important feature of this method.
Tetrahedron Letters | 1997
Suresh Iyer; C. Ramesh; Anjana Sarkar; Prakash P. Wadgaonkar
Abstract Copper (I) bromide and copper (I) iodide catalyzed the vinylation of aryl and vinyl iodides to give the corresponding vinylated products in good to high yields.
Synthetic Communications | 1989
Naganna M. Goudgaon; Prakash P. Wadgaonkar; George W. Kabalka
Abstract Borohydride supported on an ion exchange resin selectively reduced α,β-unsaturated nitroalkenes to nitroalkanes in high yields. The isolation of pure products by simple filtration is a key feature of this method.
Synthetic Communications | 1990
George W. Kabalka; Sunil M. Deshpande; Prakash P. Wadgaonkar; Narayana Chatla
The usefulness of sodium percarbonate, an inexpensive, safe and easily handled reagent for the transformation of nitriles into amides was investigated. Aromatic nitriles lacking ortho-substituents and heteroaromatic nitriles were efficiently transformed into amides; while ortho-substituted aromatic nitriles and aliphatic nitriles gave moderate yields of the corresponding amides.
Synthetic Communications | 1999
Vidyadhar K. Jadhav; Prakash P. Wadgaonkar; Prafulla L. Joshi; Manikrao M. Salunkhe
Abstract A variety of aldoximes and ketoximes are oxidised to corresponding aldehydes and ketones in excellent yields by zeolite supported permanganate
Synthetic Communications | 2000
Manojkumar R. Shukla; Prashant N. Patil; Prakash P. Wadgaonkar; Prafulla N. Josh; Manikrao M. Salunkhe
Abstract Synthesis of substituted (±)-3,4 Dihydrocoumarins were prepared with the reaction between substituted cinnamic acid and phenol catalysed by ecofriendly solid-acid catalyst H-Y zeolite involving esterification followed by ring closure.
Tetrahedron Letters | 1989
George W. Kabalka; Prakash P. Wadgaonkar; Timothy Shoup
Abstract Sodium percarbonate, a readily available, inexpensive and easy to handle reagent, efficiently oxidizes organoboranes. The yields of alcohols are essentially identical to those obtained using standard oxidation procedure.
Synthetic Communications | 2001
Vidyadhar K. Jadhav; Ravindra R. Pal; Prakash P. Wadgaonkar; Manikrao M. Salunkhe
A simple and convenient synthesis of aryl thiocyanates in high yields using sodium perborate is described.