Ken‐ichi Fuhshuku - Concepedia

Author

Ken‐ichi Fuhshuku

Keio University ORCID

Also Known As

Fuhshuku, K., K. Fuhshuku, Ken-Ichi Fuhshuku, Ken-ichi FUHSHUKU, Ken-ichi Fuhshuku, Ken‐ichi Fuhshuku

Publications

463

Citations

H-Index

Concepts

All Affiliations

Keio University Toyama Prefectural University RIKEN

About

Ken‐ichi Fuhshuku is an author at Keio University specializing in biochemistry, engineering, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	10	10	296
2	Engineering	9	9	265
3	Natural Sciences	9	9	273
4	Medicine	3	3	79
5	Public Health	1	1	11

Ken‐ichi Fuhshuku

Publications

420

Citations

H-Index

Page 1

	Year	Citations
Synthesis of (R)-β-nitro alcohols catalyzed by R-selective hydroxynitrile lyase from Arabidopsis thaliana in the aqueous–organic biphasic system Ken‐ichi Fuhshuku, Yasuhisa Asano Journal of Biotechnology BiosynthesisEngineeringArabidopsis ThalianaBiochemistryR-selective Hydroxynitrile Lyase	2011	63
Access to Wieland−Miescher Ketone in an Enantiomerically Pure Form by a Kinetic Resolution with Yeast-Mediated Reduction Ken‐ichi Fuhshuku, Nobutaka Funa, Tomohiro Akeboshi, The Journal of Organic Chemistry	1999	47
S-selective hydroxynitrile lyase from a plant Baliospermum montanum: Molecular characterization of recombinant enzyme Mohammad Dadashipour, Mizue Yamazaki, Kazumi Momonoi, Journal of Biotechnology S-selective Hydroxynitrile LyaseEngineeringBiochemistryPlant Baliospermum MontanumNatural Sciences	2011	45
RCAI-8, 9, 18, 19, and 49–52, conformationally restricted analogues of KRN7000 with an azetidine or a pyrrolidine ring: Their synthesis and bioactivity for mouse natural killer T cells to produce cytokines Ken‐ichi Fuhshuku, Naomi Hongo, Takuya Tashiro, Bioorganic & Medicinal Chemistry Pyrrolidine RingMedicineImmunologyImmune RegulationImmunodominance	2007	45
First total synthesis of modiolide A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone Masaaki Matsuda, Takahiro Yamazaki, Ken‐ichi Fuhshuku, Tetrahedron BiosynthesisPropargyl KetoneEngineeringBiochemistryEnantioselective Synthesis	2007	30
Realization of the synthesis of α,α-disubstituted carbamylacetates and cyanoacetates by either enzymatic or chemical functional group transformation, depending upon the substrate specificity of Rhodococcus amidase Masahiro Yokoyama, Mieko Kashiwagi, Masakazu Iwasaki, Tetrahedron Asymmetry BiosynthesisRhodococcus Amidaseα-Disubstituted CarbamylacetatesBiochemistryEngineering	2004	26
Control of the nitrile-hydrolyzing enzyme activity in Rhodococcus rhodochrous IFO 15564: preferential action of nitrile hydratase and amidase depending on the reaction condition factors and its application to the one-pot preparation of amides from aldehydes Mieko Kashiwagi, Ken‐ichi Fuhshuku, Takeshi Sugai Journal of Molecular Catalysis B Enzymatic BiosynthesisEngineeringOne-pot PreparationBiochemistryNatural Sciences	2004	25
Enantiomerically Pure Octahydronaphthalenone and Octahydroindenone: Elaboration of the Substrate Overcame the Specificity of Yeast‐Mediated Reduction Ken‐ichi Fuhshuku, Mina Tomita, Takeshi Sugai Advanced Synthesis & Catalysis EngineeringMolecular BiologyOrganic ChemistryCarbonyl GroupChemical Biology	2003	24
Screening, substrate specificity and stereoselectivity of yeast strains, which reduce sterically hindered isopropyl ketones Chihiro Hiraoka, Masaaki Matsuda, Yuya Suzuki, Tetrahedron Asymmetry Yeast StrainsBiochemistryNatural SciencesSubstrate SpecificityBiotechnology	2006	23
A Simple Enzymatic Method for Production of a Wide Variety of <scp>D</scp>-Amino Acids Using <scp>L</scp>-Amino Acid Oxidase from <i>Rhodococcus</i> sp. AIU Z-35-1 Kimiyasu Isobe, Hiroshi Tamauchi, Ken‐ichi Fuhshuku, Enzyme Research EngineeringSimple Enzymatic MethodEnzymatic ModificationWide VarietyBiosynthesis	2010	23

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