biblio
“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.
, “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.
, “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.
, “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.
, “Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation”, Carbohydrate Research, vol. 344, no. 10, pp. 1159-1166, 2009.
, “Formal synthesis of valiolamine from myo-inositol”, Tetrahedron, vol. 67, no. 41, pp. 7963-7970, 2011.
, “Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol”, Tetrahedron Letters, vol. 52, no. 29, pp. 3756-3758, 2011.
, “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.
, “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.
, “Myo-Inositol 1,3-acetals as early intermediates during the synthesis of cyclitol derivatives”, Carbohydrate Research, vol. 399, no. 4, pp. 8-14, 2014.
, “Asymmetric synthesis of inositol derivatives”, Tetrahedron, vol. 162, p. 134113, 2024.
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