Facile Synthesis of 6^1-O-(α-D-Galactopyranosyl)cyclomaltoheptaose from Commercially Available Branched Cyclodextrin

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Regioselective Mono-2-C-iodination of Fully Methylated Cyclodextrins through Interconversions between Cyclic and Acyclic Structures
Preparation and Characterization of Novel Carbosilane Dendrimers Carrying Mesogens
Preparation of New Carbosilane Dendrimers Carrying Mesogenic Groups
Facile Synthesis of 6^1-O-(α-D-Galactopyranosyl)cyclomaltoheptaose from Commercially Available Branched Cyclodextrin
Synthesis of Amphiphilic Chitopentaose and Chitoheptaose Derivative Using a Common Disaccharidic Synthon as the Chain Elongation Unit
Efficient and Regioselective Preparation of an Eight-membered Interglycosidic Benzylidene Derivative of β-Cyclodextrin
Synthesis of Carbosilane Compounds Functionalized with Three or Four β-Cyclodextrin Moieties. Use of a One-Pot Reaction in Liquid Ammonia for Birch Reduction and the Subsequent S_N2 Replacement
Preparation of a Demethylallosamidin Isomer Having an N,N'-Diacetylchitobiosyl Moiety and Its Potent Inhibition against Yeast Chitinase
Synthesis of a New Allosamidin Analog, N,N'-Diacetyl-β-Chitobiosyl Allosamizoline, and Its Inhibitory Activity against Some Chitinases
Preparation and Characterization of Carbosilane Dendrimers Carrying Mesogens with Chiral Substituent
Synthesis of a Potential Heparanase Inhibitor
Design and Synthesis of a Potential Endoglycosidase Inhibitor : Chemical Conversion of N, N′-Diacetylchitobiose into Novel Pseudodisaccharide Containing a Fivemembvered Cyclic N, N-Dimethylguanidine
Preparation and Characterization of Water-Soluble Polysilanes Bearing Chiral Pendant Ammonium Moieties
Preparation of Amphiphilic Polysilanes Bearing Chiral Pendant Ammonium Moieties
Syntheses of L-Fucopyranose and Its Homologs with Ring Heteroatoms Other than Oxygen. Stereocontrolled Conversion of a Common D-Arabinofuranoside Intermediate
The use of Grignard reagents in the synthesis of carbohydrates. III. The one-way anomerization of methyl glycofuranosides and the opening of their furanose rings.
Preferential introduction of a pyridylmethyl group into sulfonamides as an approach to an intramolular transimination.
Asymmetric synthesis of .ALPHA.-deuterated .ALPHA.-amino acids through nonenzymatic transamination reaction and the determination of their enantiomeric excesses.
Optical resolution of pyridoxal-like pyridinophanes.
A kinetic study of a Zn2+-catalyzed transamination reaction between pyridoxamine analogs with a pyridinophane structure and .ALPHA.-keto acids.

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