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N.  Hiyoshi, Mine, E., Rode, C. V., Sato, O., Ebina, T., and Shirai, M., ?Control of stereoselectivity in 4-tert-butylphenol hydrogenation over a carbon-supported rhodium catalyst by carbon dioxide solvent?, Chemistry Letters, vol. 35, no. 9, pp. 1060-1061, 2006.\par \par C. V.  Rode, Kshirsagar, V. S., Nadgeri, J. M., and Patil, K. R., ?Cobalt-salen intercalated montmorillonite catalyst for air oxidation of p-cresol under mild conditions?, Industrial & Engineering Chemistry Research, vol. 46, no. 25, pp. 8413-8419, 2007.\par \par C. V.  Rode, ?Catalytic hydrogenation of 2-butyne-1,4-diol: activity, selectivity and kinetics studies?, Journal of the Japan Petroleum Institute, vol. 51, no. 3, pp. 119-133, 2008.\par \par A. C.  Garade, Hengne, A. M., Deshpande, T. N., Shaligram, S. V., Shirai, M., and Rode, C. V., ?Continuous hydroxyalkylation of p-Cresol to 2,2 `-methylenebis(4-Methylphenol) in a fixed bed reactor?, Journal of Chemical Engineering of Japan, vol. 42, no. 10, pp. 782-787, 2009.\par \par R. B.  Mane, Hengne, A. M., Ghalwadkar, A. A., Vijayanand, S., Mohite, P. H., Potdar, H. S., and Rode, C. V., ?Cu:Al Nano catalyst for selective hydrogenolysis of glycerol to 1,2-propanediol?, Catalysis Letters, vol. 135, no. 1-2, pp. 141-147, 2010.\par \par J. M.  Nadgeri, Biradar, N. S., Patil, P. B., Jadkar, S. T., Garade, A. C., and Rode, C. V., ?Control of competing hydrogenation of phenylhydroxylamine to aniline in a single-step hydrogenation of nitrobenzene to p-aminophenol?, Industrial & Engineering Chemistry Research, vol. 50, no. 9, pp. 5478-5484, 2011.\par \par R. B.  Mane and Rode, C. V., ?Continuous dehydration and hydrogenolysis of glycerol over non-chromium copper catalyst: laboratory-scale process studies?, Organic Process Research & Development, vol. 16, no. 5, pp. 1043-1052, 2012.\par \par A. M.  Hengne and Rode, C. V., ?Cu-ZrO2 nanocomposite catalyst for selective hydrogenation of levulinic acid and its ester to gamma-valerolactone?, Green Chemistry, vol. 14, no. 4, pp. 1064-1072, 2012.\par \par S. B.  Kamble and Rode, C. V., ?Cascade synthesis of 2-cyanoacrylamides through deacetalization and/or knoevenagelcondensation followed by selective monohydration of acetals and aldehydes over solid acidferrites?, Chemcatchem, vol. 8, no. 16, pp. 2678-2687, 2016.\par \par A.  Jha, Jeong, D. - W., Lee, Y. - L., Jang, W. - J., Shim, J. - O., Jeon, K. - W., Rode, C. V., and Roh, H. - S., ?Chromium free high temperature water-gas shift catalyst for the production of hydrogen from waste derived synthesis gas?, Applied Catalysis A-General, vol. 522, pp. 21-31, 2016.\par \par A.  Basu, Roy, K., Sharma, N., Nandi, S., Vaidhyanathan, R., Rane, S., Rode, C. V., and Ogale, S. B., ?CO2 Laser direct written MOF-based metal-decorated and heteroatom-doped porous graphene for flexible all-solid-state microsupercapacitor with extremely high cycling stability?, ACS Applied Materials & Interfaces, vol. 8, no. 46, pp. 31841-31848, 2016.\par \par S. S.  Sable, Ghute, P. P., Fakhrnasova, D., Mane, R. B., Rode, C. V., Medina, F., and Contreras, S., ?Catalytic ozonation of clofibric acid over copper-based catalysts: in situ ATR-IR studies?, Applied Catalysis B-Environmental, vol. 209, pp. 523-529, 2017.\par \par S. S.  Sakate, Shinde, S. H., Kasar, G. B., Chikate, R. C., and Rode, C. V., ?Cascade synthesis of dihydrobenzofuran via claisen rearrangement of allyl aryl ethers using FeCl 3 /MCM-41 catalyst?, Journal of Saudi Chemical Society, vol. 22, no. 4, pp. 396-404, 2018.\par \par S. S.  Shaikh, Patil, C. R., Kondawar, S. E., and Rode, C. V., ?Cooperative acid-base sites of solid Ba-Zr mixed oxide catalyst for efficient isomerization of glucose to fructose in aqueous medium?, ChemistrySelect, vol. 5, no. 40, pp. 12505-12513, 2020.\par \par K.  Taniguchi, Kusumawati, E. N., Nanao, H., Rode, C. V., Sato, O., Yamaguchi, A., and Shirai, M., ?Conversion of benzyl phenyl ether to monoaromatics in high-temperature aqueous ethanol solution under high-pressure carbon dioxide conditions?, New Journal of Chemistry, vol. 47, no. 27, pp. 12561-12569, 2023.\par \par }