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Publications by Koichiro Naemura
Facile Preparation of Optically Active Bicyclo[3.3.1]nonane-2,6-Diol and 3,3,7,7-Tetramethylbicyclo[3.3.1]nonane-2,6-Diol by Enzyme-Catalyzed Hydrolysis, and Enantiomer Recognition Behavior of Crown Ethers and Podands Having These Diols as a Chiral Subunit
Bulletin of the Chemical Society of Japan
Chemistry
Preparation and Chiroptical Properties of Optically Active Tetracyclic Cage-Shaped Hydrocarbons; [M.0]Triblattanes and [M.1]Triblattanes
Bulletin of the Chemical Society of Japan
Chemistry
Related publications
Preparation of Bicyclo[3.3.1]nonane-2,4-Dione Derivatives
Bulletin of the Chemical Society of Japan
Chemistry
Synthesis of Bicyclo[3.3.1]nonane Derivatives Containing Fused Heterocyclic Rings
Arkivoc
Organic Chemistry
Synthesis of Star-Shaped Aromatic Derivatives With Chirality Predetermined by Bicyclo[3.3.1]nonane Framework
Synlett
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An Unusual Michael-Induced Skeletal Rearrangement of a Bicyclo[3.3.1]nonane Framework of Phloroglucinols to a Novel Bioactive Bicyclo[3.3.0]octane
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Progress Toward the Synthesis of Garsubellin a and Related Phloroglucins: The Direct Diastereoselective Synthesis of the Bicyclo[3.3.1]nonane Core†
Organic Letters
Biochemistry
Organic Chemistry
Theoretical Chemistry
Physical
Powder Study of 3-Azabicyclo[3.3.1]nonane-2,4-Dione 1-Methylnaphthalene Hemisolvate
Acta Crystallographica Section E Structure Reports Online
Chiral Recognition Abilities of New Optically Active Polyurethanes Derived From Chiral 1,3-Diols and Diisocyanates
Polymer Journal
Polymers
Materials Chemistry
Plastics
Facile Synthesis of Optically Active Oxindoles by Copper-Catalyzed Asymmetric Monotosylation of Prochiral 1,3-Diols
Tetrahedron Asymmetry
Organic Chemistry
Inorganic Chemistry
Catalysis
Theoretical Chemistry
Physical
Lewis Acid Catalyzed Tandem 1,4-Conjugate Addition/Cyclization of in Situ Generated Alkynyl oQuinone Methides and Electron-Rich Phenols: Synthesis of Dioxabicyclo[3.3.1]nonane Skeletons
