<style face="normal" font="default" size="100%">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</style>

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<style face="normal" font="default" size="100%">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</style>

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<style face="normal" font="default" size="100%">Sulfonate protecting groups. synthesis of O- and C-methylated inositols: D- and L-ononitol, D- and L-laminitol, mytilitol and scyllo-inositol methyl ether</style>

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<style face="normal" font="default" size="100%">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</style>

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<style face="normal" font="default" size="100%">Inositol derived crown ethers: effect of auxiliary protecting groups and the relative orientation of crown ether oxygen atoms on their metal ion binding ability</style>

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<style face="normal" font="default" size="100%">Regioselective O-acylation of myo-inositol 1,3,5-orthoesters: dependence of regioselectivity on the stoichiometry of the base</style>

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<style face="normal" font="default" size="100%">Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation</style>

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<style face="normal" font="default" size="100%">Conformational polymorphism in racemic 2,4-Di-o-Benzoyl-6-o-Tosyl myo-Inositol 1,3,5-Orthoacetate</style>

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<style face="normal" font="default" size="100%">Intramolecular hydrogen abstraction in radicals derived from inositol 1,3-acetals: efficient access to cyclitols</style>

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<style face="normal" font="default" size="100%">Orthogonally protected cyclohexanehexols by a ``one reaction - one product'' approach: efficient access to cyclitols and their analogs</style>

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<style face="normal" font="default" size="100%">Formal synthesis of valiolamine from myo-inositol</style>

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<style face="normal" font="default" size="100%">Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol</style>

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<style face="normal" font="default" size="100%">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</style>

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<style face="normal" font="default" size="100%">Radical mediated deoxygenation of inositol benzylidene acetals: conformational analysis, DFT calculations, and mechanism</style>

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<style face="normal" font="default" size="100%">Orientation of the beta-hydroxyl group controls the diastereoselectivity during the hydride reduction and grignard reaction of inososes</style>

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<style face="normal" font="default" size="100%">Myo-Inositol 1,3-acetals as early intermediates during the synthesis of cyclitol derivatives</style>

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<style face="normal" font="default" size="100%">Asymmetric synthesis of inositol derivatives</style>

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<style face="normal" font="default" size="100%">Desymmetrization of myo-inositol</style>