Drupal-Biblio17<style face="normal" font="default" size="100%">Subtle crossover from C-H center dot center dot center dot O to S=O center dot center dot center dot C=O short contacts in the association of diastereomers of 2,4(6)-di-O-benzoyl-6(4)-O-[(1S)-10-camphorsulfonyl]-myo-inositol 1,3,5-orthoformate upon format</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Investigating organization of molecules that facilitates intermolecular acyl transfer in crystals: reactivity and x-ray structures of O-benzoyl-myo-inositol 1,3,5-orthoesters</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Crystal-to-crystal transformation amongst dimorphs of racemic 2,6-di-O-(p-halobenzoyl)-myo-inositol 1,3,5-orthoformates that achieves halogen bonding contacts</style>Drupal-Biblio17<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>Drupal-Biblio17<style face="normal" font="default" size="100%">Enhancing intermolecular benzoyl-transfer reactivity in crystals by growing a ``reactive'' metastable polymorph by using a chiral additive</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Isostructural molecular strings linked via conserved dipolar (ether) O center dot center dot center dot C=O short contacts in conformational polymorphs of racemic 2,4-di-O-acetyl-6-O-tosyl-myo-inositol 1,3,5-orthoesters</style>Drupal-Biblio17<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>Drupal-Biblio17<style face="normal" font="default" size="100%">Relative reactivity of hydroxyl groups in inositol derivatives: role of metal ion chelation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Two modes of O-H center dot center dot center dot O hydrogen bonding utilized in dimorphs of racemic 6-O-acryloyl-2-O-benzoyl-myo-inositol 1,3,5-orthoformate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Crystal-to-crystal thermal phase transition amongst dimorphs of hexa-O-p-toluoyl-myo-inositol conserving two-dimensional isostructurality</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Helical self-assembly of molecules in pseudopolymorphs of racemic 2,6-di-O-(4-halobenzoyl)-myo-inositol 1,3,5-orthoformates: clues for the construction of molecular assemblies for intermolecular acyl transfer reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Intramolecular hydrogen abstraction in radicals derived from inositol 1,3-acetals: efficient access to cyclitols</style>Drupal-Biblio17<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>Drupal-Biblio17<style face="normal" font="default" size="100%">Comparison of racemic epi-inosose and (-)-epi-inosose</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of valiolamine from myo-inositol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Intermolecular benzoyl group transfer reactivity in crystals of racemic 2,6-di-O-benzoyl-myo-inositol 1,3,5-orthobenzoate: controlling reactivity by solvate (pseudopolymorph) formation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Protecting group directed stereoselective reduction of an epi-inosose: efficient synthesis of epi-inositol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Thermal epimerization of inositol 1,3-benzylidene acetals in the molten state</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Achieving molecular stability of racemic 4-O-benzyl-myo-inositol-1,3,5-orthoformate through crystal formation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Chiral crystals from an achiral molecule: 4,6-di-O-benzyl-1,3-O-benzylidene-2-O-(4-methoxybenzyl)-myo-5-inosose</style>Drupal-Biblio17<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>Drupal-Biblio17<style face="normal" font="default" size="100%">Radical mediated deoxygenation of inositol benzylidene acetals: conformational analysis, DFT calculations, and mechanism</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Solvent induced crystallization of 1,2,3,4(6),5-penta-O-acetyl-6(4)-O-[(1S)-10-camphor sulfonyl]-myo-inositol diastereomers associated via weak trifurcated C-H center dot center dot center dot O interactions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of the aminocyclitol units of (-)-hygromycin a and methoxyhygromycin from myo-inositol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of molecular crystals capable of undergoing an acyl-transfer reaction based on intermolecular interactions in the crystal lattice</style>Drupal-Biblio17<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>Drupal-Biblio17<style face="normal" font="default" size="100%">Acyl-transfer reactions in molecular crystals: reactivity correlation with crystal structure</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Correlation of the solid-state reactivities of racemic 2,4(6)-di-O-benzoyl-myo-inositol 1,3,5-orthoformate and its 4,4 `-bipyridine cocrystal with their crystal structures</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Crystal-to-crystal thermal phase transformation of polymorphs of isomeric 2,3-naphthalene diol ditoluates: mechanism and implications for molecular crystal formation and melting</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Myo-Inositol 1,3-acetals as early intermediates during the synthesis of cyclitol derivatives</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Cocrystallization of 2,3-dihydroxynaphthalene with its para-, meta-, and ortho-ditoluates: insight into cocrystal formation and clues for the construction of supramolecular assemblies capable of intermolecular acyl group transfer reactivity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Intramolecular cyclization of carbonate and thiocarbonate derivatives of myo-inositol in the solid state: implications for acyl group transfer reactions in molecular crystals</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Engineering crystals that facilitate the acyl-transfer reaction: insight from a comparison of the crystal structures of myo-inositol-1,3,5-orthoformate-derived benzoates and carbonates</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Clues from crystal structures pave the way to access chiral myo-inositol derived versatile synthons: resolution of racemic 4-o-allyl-myo-inositol-1,3,5-orthoesters via corresponding dicamphanates by crystallization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Helical preorganization of molecules drives solid-state intermolecular acyl-transfer reactivity in crystals: structures and reactivity studies of solvates of racemic 2,6-Di-O-(4-fluorobenzoyl)-myo-inositol 1,3,5-orthoformate</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Correlation of intermolecular acyl transfer reactivity with noncovalent lattice interactions in molecular crystals: toward prediction of reactivity of organic molecules in the solid state</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Effect of crystal packing on the thermosalient effect of the pincer-type diester naphthalene-2,3-diyl-bis(4-fluorobenzoate): a new class II thermosalient solid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Inositol to aromatics -benzene free synthesis of poly oxygenated aromatics</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> Lithium hydride as an efficient reagent for the preparation of 1,2-anhydro inositols: does the reaction proceed through 'axial rich' conformation?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Cocrystallization of 2,3-dihydroxynaphthalene with its para-, meta-, and ortho-ditoluates: insight into cocrystal formation and clues for the construction of supramolecular assemblies capable of intermolecular acyl group transfer reactivity (vol 15, pg 12</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> Intermolecular acyl-transfer reactions in molecular crystals </style>Drupal-Biblio17<style face="normal" font="default" size="100%">Access to enantiomeric organic compounds with potential for synthesis via racemic conglomerates: inositol derivatives as a case in point</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Construction of two-component chemically reactive supramolecular assemblies-acyl migration reactions in cocrystals of napthalene-2,3-diol and its diesters</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Palladium mediated selective cleavage of benzyl and allyl phosphates: a convenient non-hydrogenolytic method for the synthesis of phosphates and phospholipids.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Desymmetrization of myo-inositol</style>