Haruhiko Kusaka - Concepedia

Author

Haruhiko Kusaka

Mitsubishi Chemical (Japan)

Also Known As

H. KUSAKA, Haruhiko Kusaka

Publications

283

Citations

H-Index

Concepts

All Affiliations

Mitsubishi Chemical (Japan)Niigata University Tohoku University

About

Haruhiko Kusaka is an author at Mitsubishi Chemical (Japan) specializing in engineering, chemistry, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	6	6	199
2	Natural Sciences	2	2	89
3	Biochemistry	2	2	89
4	Biomolecular Engineering	2	2	57
5	Biomedical Engineering	1	1	45

Haruhiko Kusaka

Publications

279

Citations

H-Index

Page 1

	Year	Citations
A Novel Production of γ-Butyrolactone Catalyzed by Ruthenium Complexes Yoshinori Hara, Haruhiko Kusaka, Hiroko Inagaki, Journal of Catalysis Inorganic ChemistryEngineeringRuthenium ComplexesMolecular ComplexCatalysis	2000	64
Studies on the syntheses of sesquiterpene lactones. 11. The syntheses of 3-epizaluzanin C, zaluzanin C, zaluzanin D, and related compounds 3.alpha.-hydroxyguaia-1(10),4(15),11(13)-trieno-12,6.alpha.-lactone and 3.alpha.-hydroxyguaia-4(15),9,11(13)-trieno-12,6.alpha.-lactone Masayoshi Ando, Haruhiko Kusaka, Hiroshi Ohara, The Journal of Organic Chemistry Bioorganic ChemistryBiochemistryDonut IconNatural SciencesZaluzanin D	1989	48
Nanopillar Polymer Films as Antibacterial Packaging Materials Denver P. Linklater, Soichiro Saita, T. Murata, ACS Applied Nano Materials Materials ScienceComprehensive Analytical SurveyAntimicrobial PackagingEngineeringPolymer Nanotechnology	2022	45
Studies on the syntheses of sesquiterpene lactones. 10. Improved syntheses of (+)-tuberiferin and the related .alpha.-methylene-.gamma.-lactones and their biological activities Masayoshi Ando, Tetsuo Wada, Haruhiko Kusaka, The Journal of Organic Chemistry Sesquiterpene LactonesBiosynthesisBioorganic ChemistryEngineeringBiochemistry	1987	41
A Novel Synthetic Method of the (±)-(3aα,8aα)-Ethyl 8β-Hydroxy-6β-methyl-2-oxooctahydro-2<i>H</i>-cyclohepta[<i>b</i>]furan-3α- carboxylate and Its Chemical Transformation to (±)-(3aα,8aα)-3α,6β-Dimethyl-3,3a,4,5,6,8a-hexahydro-2<i>H</i>- cyclohepta[<i>b</i>]furan-2-one, (+)- and (−)-7β-(2-Acetoxy-1α-methylethyl)-4β-methyl-2-cyclohepten-1β-ol, and (+)- and (−)-7β-(2-Acetoxy-1α-methylethyl)-4β-methyl-2-cyclohepten-1-one. Possible Common Synthetic Intermediates for Pseudoguaianolides, 4,5-Secopseudoguaianolides, Guaianolides, 4,5-Secoguaianolides, and Octalactins Fumito Shimoma, Haruhiko Kusaka, Katsuaki Wada, The Journal of Organic Chemistry	1998	32
Catalytic Asymmetric Aldol Reaction of Ketene Silyl Acetals with Aldehydes by Use of Chiral Bissulfonamido Zinc(II) Teruaki Mukaiyama, Tohru Takashima, Haruhiko Kusaka, Chemistry Letters Chemical EngineeringEngineeringOrganic ChemistryOrganometallic CatalysisCatalysis	1990	19
Total Syntheses of (±)-Hymenolin and (±)-Parthenin Fumito Shimoma, Haruhiko Kusaka, Hidenori Azami, The Journal of Organic Chemistry BiosynthesisEngineeringDonut IconAltmetric Attention ScoreNatural Product Biosynthesis	1998	16
Characterization and Nitrile Group Hydrogenation Study of Supported and Unsupported Ru–Co Catalyst Haruhiko Kusaka, Yoshinori Hara, Masamichi Onuki, Journal of Catalysis Materials ScienceInorganic ChemistryEngineeringHeterogeneous CatalysisCatalysis	1996	14

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