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S. S.  Chavan, Rupanawar, B. D., Kamble, R. B., Shelke, A. M., and Suryavanshi, G., ?Metal-free annulation of ?-acylamino ketones: facile access to spirooxazolines and oxazolines via oxidative C?O bond formation?, Organic Chemistry Frontiers , vol. 5, no. 4, pp. 544-548 , 2018.\par \par B. D.  Rupanawar, Veetil, S. M., and Suryavanshi, G., ?Oxidative Olefination of Benzylamine with an Active Methylene Compound Mediated by Hypervalent Iodine (III)?, European Journal of Organic Chemistry, 2019.\par \par R. B.  Kamble, Mane, K. D., Rupanawar, B. D., Korekar, P., Sudalai, A., and Suryavanshi, G., ?Ti-superoxide catalyzed oxidative amidation of aldehydes with saccharin as nitrogen source: synthesis of primary amides?, RSC Advances, vol. 10, no. 2, pp. 724-728, 2020.\par \par V.  Ramavath, Rupanawar, B. D., More, S. G., Bansode, A. H., and Suryavanshi, G., ?Hypervalent iodine(iii) induced oxidative olefination of benzylamines using Wittig reagents?, New Journal of Chemistry, vol. 45, no. 19, pp. 8806-8813, 2021.\par \par S. G.  More, Rupanawar, B. D., and Suryavanshi, G., ?Metal-free, acid-catalyzed 1,6-conjugate addition of NH-sulfoximines to para-quinone methides: accessing to diarylmethine imino sulfanone?, Journal of Organic Chemistry, vol. 86, no. 15, pp. 10129-10139, 2021.\par \par B. D.  Rupanawar, Mane, K. D., and Suryavanshi, G., ?Hypervalent-iodine-mediated oxidation followed by the acetoxylation/tosylation of alpha-substituted benzylamines to obtain alpha-acyloxy/tosyloxy ketones?, New Journal of Chemistry, vol. 46, no. 35, pp. 16832-16839, 2022.\par \par K. D.  Mane, Rupanawar, B. D., and Suryavanshi, G., ?Visible light-promoted, photocatalyst-free C(sp(2))-H bond functionalization of indolizines via EDA complexes?, European Journal of Organic Chemistry, vol. 2022, no. 18, p. e202200261, 2022.\par \par B. D.  Rupanawar, Bansode, A. H., and Suryavanshi, G., ?Hypervalent-iodine-mediated base-free oxidative olefination of benzylic amines to access ?,?-unsaturated ketones?, Synlett, vol. 36, no. 5, pp. 556-560, 2025.\par \par }