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Journal Article
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.
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.
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.
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.
R. C. Jagdhane and Shashidhar, M. S., Formal synthesis of valiolamine from myo-inositol, Tetrahedron, vol. 67, no. 41, pp. 7963-7970, 2011.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.