Syun‐ichi Kiyooka - Concepedia

Author

Syun‐ichi Kiyooka

Also Known As

SYUN'ICHI KIYOOKA, SYUN‐ICHI KIYOOKA, Syun-ichi KIYOOKA, Syun-ichi Kiyooka, Syunichi Kiyooka, Syun‐ichi Kiyooka, Syun’ichi Kiyooka

105

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Kōchi University Akebono (Japan)Kyushu University Otsuka (Japan)

About

Syun‐ichi Kiyooka is an author at Kōchi University specializing in organic chemistry, engineering, and chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	20	36	1.1K
2	Biomolecular Engineering	17	22	727
3	Natural Sciences	13	15	679
4	Biochemistry	12	12	606
5	Health Sciences	1	1	35

Syun‐ichi Kiyooka

Publications

Citations

H-Index

Page 1

	Year	Citations
Enantioselective chiral borane-mediated aldol reactions of silyl ketene acetals with aldehydes. The novel effect of the trialkysilyl group of the silyl ketene acetal on the reaction course Syun‐ichi Kiyooka, Yuichi Kaneko, Misako Komura, The Journal of Organic Chemistry Silyl Ketene AcetalsBiochemistryReaction CourseSilyl Ketene AcetalNatural Sciences	1991	197
1,3-syn diastereoselective reduction of β-hydroxyketones with diisobutylaluminum hydride and tributyltin hydride Syun‐ichi Kiyooka, Hisanori Kuroda, Yayoi Shimasaki Tetrahedron Letters 1,3-Syn Diastereoselective ReductionDiisobutylaluminum HydrideBiochemistryNatural SciencesTributyltin Hydride	1986	127
The catalytic asymmetric aldol reaction of silyl ketene acetals with aldehydes in the presence of a chiral borane complex. Nitroethane as a highly effective solvent for catalytic conditions Syun‐ichi Kiyooka, Yuichi Kaneko, Ken-ichi Kume Tetrahedron Letters EngineeringEffective SolventChiral Borane ComplexOrganic ChemistryOrganometallic Catalysis	1992	118
Acyclic stereoselection. 22. Diastereofacial selectivity in the Lewis acid mediated reactions of allylsilanes with chiral aldehydes and enones Clayton H. Heathcock, Syun‐ichi Kiyooka, Todd A. Blumenkopf The Journal of Organic Chemistry Asymmetric CatalysisCross-coupling ReactionEngineeringLewis AcidAcyclic Stereoselection	1984	102
A Study Directed to the Asymmetric Synthesis of the Antineoplastic Macrolide Acutiphycin under Enantioselective Acyclic Stereoselection Based on Chiral Oxazaborolidinone-Promoted Asymmetic Aldol Reactions Syun‐ichi Kiyooka, Mostofa Abu Hena The Journal of Organic Chemistry Bioorganic ChemistryEngineeringAldo-keto ReductaseOrganic ChemistryStereoselective Synthesis	1999	76
Parr’s index to describe both electrophilicity and nucleophilicity Syun‐ichi Kiyooka, Daisuke Kaneno, Ryoji Fujiyama Tetrahedron Letters Parr ’Nucleic Acid ChemistryMolecular BiologyPhilosophy Of Chemistry	2012	61
A mild aldol reaction of aryl aldehydes through palladium-catalyzed hydrosilation of α,β-unsaturated carbonyl compounds with trichlorosilane Syun‐ichi Kiyooka, Atsushi Shimizu, S. TORII Tetrahedron Letters Cross-coupling ReactionMild Aldol ReactionEngineeringPalladium-catalyzed HydrosilationOrganic Chemistry	1998	58
Dramatic changes in diastereoselectivity with the quantity of titanium tetrachloride used in Lewis acid mediated reactions of allylsilane with .alpha.-amino aldehydes Syun‐ichi Kiyooka, Masahito Nakano, Fuminori Shiota, The Journal of Organic Chemistry Chemical EngineeringEngineeringLewis AcidAltmetric Attention ScoreOrganic Chemistry	1989	51
Intrinsic reactivity index as a single scale directed toward both electrophilicity and nucleophilicity using frontier molecular orbitals Syun‐ichi Kiyooka, Daisuke Kaneno, Ryoji Fujiyama Tetrahedron Frontier Molecular OrbitalsMolecular ElectrochemistryNatural SciencesChemical BondIntrinsic Reactivity Index	2013	48
Acyclic stereoselection. 20. High diastereofacial selectivity in the stannic chloride mediated reactions of allylsilanes with chiral α- and β-alkoxy aldehydes. Syun‐ichi Kiyooka, Clayton H. Heathcock Tetrahedron Letters Cross-coupling ReactionHigh Diastereofacial SelectivityEngineeringAcyclic StereoselectionOrganic Chemistry	1983	46

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