@shrishivajicollege.org
Assistant Professor
Shri Shivaji College Parbhani /Swami Ramanand Teerth Marathwada University (SRTMUN), Nanded
Green Chemistry, Catalysis, Synthesis
Scopus Publications
Scholar Citations
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Bhaskar P. Ankush, Balasaheb V. Shitole, and Shitole Nana Vikram
Instituto de Quimica - Univ. Federal do Mato Grosso do Sul
Balasaheb. V. Shitole, Suraj B. Ade, and Shitole Nana Vikram
Instituto de Quimica - Univ. Federal do Mato Grosso do Sul
Potassium dihydrogen Phosphate catalyzed one-pot synthesis of 2,3-Dihydro-2-Phenyl-1H-Naphtho-[1,2-e] [1,3] Oxazine, from 2-naphthol, formalin and aromatic amine was grind by pestle and mortar without any solvent at room temperature for specified period of time. The attractive features of this process are inexpensive, efficient, as well as user friendly. DOI: http://dx.doi.org/10.17807/orbital.v11i3.1396
Nana Vikram Shitole, Balasaheb V. Shitole, and Gopal K. Kakde
Instituto de Quimica - Univ. Federal do Mato Grosso do Sul
Disodium phosphate catalyzed one-pot synthesis of 3,4-dihydropyrano[3,2-c]chromenes, from aldehydes, active methylene compounds malononitrile and 4-hydroxycoumarin in ethanol:water (1:1) under reflux temperature. The attractive features of this process are inexpensive, efficient, as well as user friendly. DOI: http://dx.doi.org/10.17807/orbital.v9i3.896
Nana V. Shitole, Kirti S. Niralwad, Bapurao B. Shingate, and Murlidhar S. Shingare
Elsevier BV
Abstract Chlorosulfonic acid (ClSO 3 H) used to be a catalyst for the synthesis of 2-aryl-1-arylmethyl-1 H -benzimidazoles which was efficiently simple and convenient. This method afforded short reaction time, easy workup, moderate to excellent isolated yields which make this protocol practical and economically attractive.
Nana V. Shitole, S. B. Sapkal, Bapurao B. Shingate, and Murlidhar S. Shingare
Korean Chemical Society
Multicomponent reactions (MCRs) have been emerged as an extremely powerful tool in combinatorial chemistry and drug discovery, since it offers sign ificant advantages over conven-tional linear step syntheses, in terms to improve classical organic reactions, promote new reactions and develop straightforward synthetic routes for bioactive heterocycles.
Nana V. Shitole, Kiran F. Shelke, Sandip A. Sadaphal, Bapurao B. Shingate, and Murlidhar S. Shingare
Informa UK Limited
Abstract Polyethylene glycol-400 has been found to be a recyclable and rapid reaction medium for the synthesis of 2-amino-4H-chromenes by the condensation of aromatic aldehyde, malononitrile, and α-naphthol. This method gives remarkable advantages such as simple work up, high yields, and a greener method by avoiding toxic catalyst and hazardous solvents.
Nana V. Shitole, Kiran F. Shelke, Sandip A. Sadaphal, Bapurao B. Shingate, and Murlidhar S. Shingare
Informa UK Limited
Abstract Polyethylene glycol-400 has been found to be a recyclable and rapid reaction medium for the synthesis of 2-amino-4H-chromenes by the condensation of aromatic aldehyde, malononitrile, and α-naphthol. This method gives remarkable advantages such as simple work up, high yields, and a greener method by avoiding toxic catalyst and hazardous solvents.
Kiran F. Shelke, Suryakant B. Sapkal, Nana V. Shitole, Bapurao B. Shingate, and Murlidhar S. Shingare
Korean Chemical Society
A simple, highly efficient and environmentally benign method for the synthesis of 3-styrylchromones from 3-formylchromones and 4-nitrophenylacetic acid/4-nitrotolune in the presence of catalytic amount of basic ionic liquid 1-butyl-3-methylimidazolium hydroxide [(bmim)OH] carried out under the influence of microwave irradiation. This method gives remarkable advantages such as, short reaction times, simple work-up procedure and moderate to good yields. The ionic liquid was successfully reused for four cycles without significant loss of activity.
S. Sadaphal, Swapnil S. Sonar, R. U. Pokalwar, Nana V. Shitole and M. Shingare
Korean Chemical Society
Sulphamic acid has been exploited as a cost-effective catalyst and green alternative for conventional acidic materials to synthesize α-hydroxy phosphonates under solvent-free condition. The reaction carried out using ultrasound irradiation with better yields and shorter reaction time.
Nana V. Shitole, K. Shelke, Swapnil S. Sonar, S. Sadaphal, B. B. Shingate and M. Shingare
Korean Chemical Society
L-Proline has been found to be an efficient organocatalyst for one-pot synthesis of 2,4,5-triaryl substituted imidazole by the reaction of an aldehyde, a benzil and an ammonium acetate. The short reaction time and excellent yields making this protocol practical and economically attractive.
Swapnil S. Sonar, S. Sadaphal, Nana V. Shitole, Nivrutti R. Jogdand, B. B. Shingate and M. Shingare
Korean Chemical Society
We have described an efficient synthesis of quino[2,3-b][1,5]benzoxazepine α-aminophosphonate derivatives by the nucleophilic addition oftriethyl phosphite to substituted quino[2,3-b][1,5]benzoxazepines promoted by easily available, inexpensive and mild catalyst KAl(SO 4 ) 2 ·12H 2 0 (alum). The reactions proceed smoothly at room temperature under solvent-free reaction conditions and providing high yield of product in very short reaction time.