Takeshi Hanamoto - Concepedia

Concepedia

Author

Takeshi Hanamoto

Kyushu University

Also Known As

Hanamoto, Hanamoto, T., T. HANAMOTO, T. Hanamoto, Takeshi HANAMOTO, Takeshi Hanamoto

83

Publications

1.4K

Citations

22

H-Index

28

Concepts

All Affiliations

Kyushu University Institute for Molecular Science Tokyo Institute of Technology Tosoh (Japan)Toyohashi University of Technology

TH

About

Takeshi Hanamoto is an author at Kyushu University specializing in organic chemistry, engineering, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	21	28	1.3K
2	Biomolecular Engineering	15	17	600
3	Biochemistry	6	6	153
4	Natural Sciences	5	5	98
5	Medicine	1	1	19

Takeshi Hanamoto

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32

Publications

1.4K

Citations

22

H-Index

	Year	Citations
Experimental Study on Heat Generation Behavior of Small Lithium-Ion Secondary Batteries Kazuo Onda, Hisashi Kameyama, Takeshi Hanamoto, Journal of The Electrochemical Society Overpotential ResistanceHeat Generation BehaviorEngineeringEnergy EfficiencyThermal Energy Storage	2003	162
Organic Synthesis with Trialkylphosphine Catalysts. Conjugate Addition of Alcohols to α,β-Unsaturated Alkynic Acid Esters Junji Inanaga, Yoshiyasu Baba, Takeshi Hanamoto Chemistry Letters Asymmetric CatalysisEngineeringCatalytic AmountTrialkylphosphine CatalystsOrganic Chemistry	1993	143
A facile reductive dimerization of conjugated acid derivatives with samarium diiodide Junji Inanaga, Yuich Handa, T. TABUCHI, Tetrahedron Letters Derivative (Chemistry)DerivativesEngineeringSamarium DiiodideOrganic Chemistry	1991	90
Remarkably High Asymmetric Amplification in the Chiral Lanthanide Complex-Catalyzed Hetero-Diels−Alder Reaction: First Example of the Nonlinear Effect in ML<sub>3</sub> System Hiroshi Furuno, Takeshi Hanamoto, Yuichi Sugimoto, Organic Letters Asymmetric CatalysisInorganic ChemistryChemical EngineeringEngineeringNonlinear Effect	1999	78
Chiral rare earth organophosphates as homogeneous Lewis acid catalysts for the highly enantioselective hetero-Diels–Alder reactions Hiroshi Furuno, Tetsuji Hayano, Takeshi Kambara, Tetrahedron Chemical EngineeringEnantioselective Hetero-diels–alder ReactionsEngineeringOrganic ChemistryCatalysis	2003	65
Asymmetric [2,3]wittig rearrangement of 2′-alkenyloxyacetamide bearing -2,5-bis(methoxymethoxymethyl)pyrrolidine moiety as a chiral auxiliary Masako Uchikawa, Takeshi Hanamoto, Tsutomu Katsuki, Tetrahedron Letters 2′-Alkenyloxyacetamide Bearing -2,5-BisEngineeringChiral AuxiliaryOrganic ChemistryPyrrolidine Moiety	1986	63
Scandium(III) Perfluorooctanesulfonate [Sc(OPf)3] : A Novel Catalyst for the Hetero Diels–Alder Reaction of Aldehydes with Non-Activated Dienes Takeshi Hanamoto, Yuichi Sugimoto, Yong Jin, Bulletin of the Chemical Society of Japan	1997	57
Highly enantioselective homogeneous catalysis of chiral rare earth phosphates in the hetero-Diels–Alder reaction Hiroshi Furuno, Takeshi Kambara, Yumiko Tanaka, Tetrahedron Letters Chemical EngineeringEngineeringEnantioselective Homogeneous CatalysisHetero-diels–alder ReactionOrganic Chemistry	2003	56
Achiral and chiral lanthanide(III) salts of superacids as novel Lewis acid catalysts in organic synthesis. Junji Inanaga, Yuki Sugimoto, Takeshi Hanamoto New Journal of Chemistry Chemical EngineeringEngineeringOrganic ChemistryCatalysisSynthetic Chemistry	1995	50
Asymmetric Hetero Diels-Alder Reaction Catalyzed by Chiral Ytterbium(III) Phosphate{Yb[(<i>R</i>)-(-)-BNP]<sub>3</sub>}: Remarkable Ligand Effect on the Enantioselectivity Takeshi Hanamoto, Hiroshi Furuno, Yuichi Sugimoto, Synlett Room TemperatureEngineeringChiral YtterbiumOrganic ChemistryOrganometallic Catalysis	2004	48

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