Atsuhito Kuboki
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Atsuhito Kuboki has a total of 20 co-authors. Here are the top co-authors by number of shared publications:
- Susumu Ohira
Department of Biological Chemistry, Faculty of Science, Okayama University of Science
4 shared publications Kohei Kuyama
2 shared publicationsMami Hamabata
2 shared publications- Takeshi Sugai
Department of Chemistry, Keio University, Hiyoshi, Yokohama 223–8522, Japan, Fax: (+81) 45–566–1697
2 shared publications Tetsuya Arishige
2 shared publicationsChie Maeda
1 shared publication
Latest Publications
- 21 July 2008
- Published by Elsevier in Tetrahedron Letters
- Vol. 49 (29-30) , 4516-4518
Total synthesis of cleomiscosin C via a regioselective cycloaddition reaction of o-quinone
- 21 July 2008
- Published by Elsevier in Tetrahedron Letters
- Vol. 49 (29-30) , 4516-4518
Total synthesis of cleomiscosin C via a regioselective cycloaddition reaction of o-quinone
- 14 April 2008
- Published by Elsevier in Tetrahedron Letters
- Vol. 49 (16) , 2558-2561
Reversal of the regioselectivity in a cycloaddition of o-quinones by varying the position of alkoxy substituents
- 14 April 2008
- Published by Elsevier in Tetrahedron Letters
- Vol. 49 (16) , 2558-2561
Reversal of the regioselectivity in a cycloaddition of o-quinones by varying the position of alkoxy substituents
- 1 January 2002
- Published by Oxford University Press (OUP) in Bioscience, Biotechnology, and Biochemistry
- Vol. 66 (4) , 887-891
Stereoselective Synthesis of (1S,3R)-1-Aminocyclopentane-1,3-dicarboxylic AcidviaC–H Insertion of Alkylidenecarbene
(1S,3R)-1-Aminocyclopentane-1,3-dicarboxylic acid (ACPD), a potent agonist of metabotropic glutamate receptors, was synthesized from L-serine. The chiral quaternary center was constructed by C-H insertion of the alkylidenecarbene, this being generated by the reaction between lithiotrimethylsilyldiazomethane and the corresponding ketone.
- 1 January 2002
- Published by Oxford University Press (OUP) in Bioscience, Biotechnology, and Biochemistry
- Vol. 66 (4) , 887-891
Stereoselective Synthesis of (1S,3R)-1-Aminocyclopentane-1,3-dicarboxylic AcidviaC–H Insertion of Alkylidenecarbene
(1S,3R)-1-Aminocyclopentane-1,3-dicarboxylic acid (ACPD), a potent agonist of metabotropic glutamate receptors, was synthesized from L-serine. The chiral quaternary center was constructed by C-H insertion of the alkylidenecarbene, this being generated by the reaction between lithiotrimethylsilyldiazomethane and the corresponding ketone.
- 1 January 1998
- Published by The Society of Synthetic Organic Chemistry, Japan in Journal of Synthetic Organic Chemistry, Japan
- Vol. 56 (6) , 489-499
Enzyme- and Microorganism-mediated Syntheses of Substances Related to Glycoconjugates.
In this article, chemo-enzymatic syntheses of important substances which serve as the building blocks for glycoconjugate synthesis are described : 1) Sialic acid aldolae-catalyzed synthesis of sialic acids and its analogs ; 2) Studies on Rhodococcus rhodochrous IFO 15564-catalyzed degradation of N-acetyl-D-glucosamine and its derivatives ; 3) Hydration of carbohydrate nitriles mediated by a nitrile hydratase produced by R. rhodochrous IFO 15564 ; 4) Synthesis of N-acetyl-D-allosamine based on the lipase-catalyzed regioselective acetylation as the key step ; 5) Kinetic optical resolution of highly deoxygenated carbohydrate by means of lipase-catalyzed transesterification ; 6) Kinetic optical resolution of ceramide based on lipase-catalyzed hydrolysis.
- 1 January 1998
- Published by The Society of Synthetic Organic Chemistry, Japan in Journal of Synthetic Organic Chemistry, Japan
- Vol. 56 (6) , 489-499
Enzyme- and Microorganism-mediated Syntheses of Substances Related to Glycoconjugates.
In this article, chemo-enzymatic syntheses of important substances which serve as the building blocks for glycoconjugate synthesis are described : 1) Sialic acid aldolae-catalyzed synthesis of sialic acids and its analogs ; 2) Studies on Rhodococcus rhodochrous IFO 15564-catalyzed degradation of N-acetyl-D-glucosamine and its derivatives ; 3) Hydration of carbohydrate nitriles mediated by a nitrile hydratase produced by R. rhodochrous IFO 15564 ; 4) Synthesis of N-acetyl-D-allosamine based on the lipase-catalyzed regioselective acetylation as the key step ; 5) Kinetic optical resolution of highly deoxygenated carbohydrate by means of lipase-catalyzed transesterification ; 6) Kinetic optical resolution of ceramide based on lipase-catalyzed hydrolysis.