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M. P.  Sarmah, Gonnade, R. G., Shashidhar, M. S., and Bhadbhade, M. M., ?Benzoyl transfer reactivities of racemic 2,4-Di-O-acyl-myo-inosityl 1,3,5-orthoesters in the solid state: molecular packing and intermolecular interactions correlate with the ease of the reaction?, Chemistry-A European Journal, vol. 11, no. 7, pp. 2103-2110, 2005.\par \par M. P.  Sarmah, Shashidhar, M. S., Sureshan, K. M., Gonnade, R. G., and Bhadbhade, M. M., ?Sulfonate protecting groups. synthesis of O- and C-methylated inositols: D- and L-ononitol, D- and L-laminitol, mytilitol and scyllo-inositol methyl ether?, Tetrahedron, vol. 61, no. 18, pp. 4437-4446, 2005.\par \par S. S.  Dixit, Shashidhar, M. S., and Devaraj, S., ?Cyclitol based metal complexing agents. preference for the extraction of lithium by myo-inositol based crown-4-ethers depends on the relative orientation of crown ether oxygen atoms?, Tetrahedron, vol. 62, no. 18, pp. 4360-4363, 2006.\par \par S. S.  Dixit and Shashidhar, M. S., ?Inositol derived crown ethers: effect of auxiliary protecting groups and the relative orientation of crown ether oxygen atoms on their metal ion binding ability?, Tetrahedron, vol. 64, no. 9, pp. 2160-2171, 2008.\par \par K. M.  Sureshan, Devaraj, S., and Shashidhar, M. S., ?Regioselective O-acylation of myo-inositol 1,3,5-orthoesters: dependence of regioselectivity on the stoichiometry of the base?, Tetrahedron, vol. 65, no. 13, pp. 2703-2710, 2009.\par \par S.  Devaraj, Jagdhane, R. C., and Shashidhar, M. S., ?Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation?, Carbohydrate Research, vol. 344, no. 10, pp. 1159-1166, 2009.\par \par K.  Manoj, Gonnade, R. G., Bhadbhade, M. M., and Shashidhar, M. S., ?Conformational polymorphism in racemic 2,4-Di-o-Benzoyl-6-o-Tosyl myo-Inositol 1,3,5-Orthoacetate?, Journal of Structural Chemistry, vol. 51, no. 4, pp. 725-730, 2010.\par \par C.  Murali, Gurale, B. P., and Shashidhar, M. S., ?Intramolecular hydrogen abstraction in radicals derived from inositol 1,3-acetals: efficient access to cyclitols?, European Journal of Organic Chemistry, no. 4, pp. 755-764, 2010.\par \par R. C.  Jagdhane and Shashidhar, M. S., ?Orthogonally protected cyclohexanehexols by a ``one reaction - one product'' approach: efficient access to cyclitols and their analogs?, European Journal of Organic Chemistry, no. 15, pp. 2945-2953, 2010.\par \par R. C.  Jagdhane and Shashidhar, M. S., ?Formal synthesis of valiolamine from myo-inositol?, Tetrahedron, vol. 67, no. 41, pp. 7963-7970, 2011.\par \par M. T.  Patil, Krishnaswamy, S., Sarmah, M. P., and Shashidhar, M. S., ?Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol?, Tetrahedron Letters, vol. 52, no. 29, pp. 3756-3758, 2011.\par \par A.  Mart and Shashidhar, M. S., ?Elaboration of the ether cleaving ability and selectivity of the classical pearlman's catalyst [Pd(OH)(2)/C]: concise synthesis of a precursor for a myo-inositol pyrophosphate?, Tetrahedron, vol. 68, no. 47, pp. 9769-9776, 2012.\par \par B. P.  Gurale, Vanka, K., and Shashidhar, M. S., ?Radical mediated deoxygenation of inositol benzylidene acetals: conformational analysis, DFT calculations, and mechanism?, Carbohydrate Research, vol. 351, pp. 26-34, 2012.\par \par R. C.  Jagdhane, Patil, M. T., Krishnaswamy, S., and Shashidhar, M. S., ?Orientation of the beta-hydroxyl group controls the diastereoselectivity during the hydride reduction and grignard reaction of inososes?, Tetrahedron, vol. 69, no. 25, pp. 5144-5151, 2013.\par \par B. P.  Gurale, Sardessai, R. S., and Shashidhar, M. S., ?Myo-Inositol 1,3-acetals as early intermediates during the synthesis of cyclitol derivatives?, Carbohydrate Research, vol. 399, no. 4, pp. 8-14, 2014.\par \par N. T.  Patil, Sarkar, N., S. Mysore, S., and Gonnade, R. G., ?Asymmetric synthesis of inositol derivatives?, Tetrahedron, vol. 162, p. 134113, 2024.\par \par N. T.  Patil, Patil, M. T., Gonnade, R. G., and Shashidhar, M. S., ?Desymmetrization of myo-inositol?, Carbohydrate Research, vol. 553, p. 109505, 2025.\par \par }