Haruro Ishitani - Concepedia

Author

Haruro Ishitani

The University of Tokyo

Also Known As

Haruro ISHITANI, Haruro Ishitani

140

Publications

7.7K

Citations

H-Index

Concepts

All Affiliations

The University of Tokyo Tokyo University of Science Tokyo Institute of Technology

About

Haruro Ishitani is an author at The University of Tokyo specializing in chemistry, catalysis, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	37	49	4.2K
2	Natural Sciences	15	15	1.2K
3	Biomolecular Engineering	14	14	1.6K
4	Biochemistry	8	8	624
5	Chemical Biology	1	1	15

Haruro Ishitani

Publications

5.8K

Citations

H-Index

Page 1

	Year	Citations
Catalytic Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst Haruro Ishitani, Masaharu Ueno, Shu̅ Kobayashi Journal of the American Chemical Society Asymmetric CatalysisInorganic ChemistryChemical EngineeringEngineeringAltmetric Attention Score	1997	276
Catalytic Asymmetric Synthesis of Both Syn- and Anti-β-Amino Alcohols Shu̅ Kobayashi, Haruro Ishitani, Masaharu Ueno Journal of the American Chemical Society Catalytic Asymmetric SynthesisEngineeringAnti-β-amino Alcoholsshū KobayashiAltmetric Attention ScoreOrganic Chemistry	1998	251
Catalytic asymmetric aza Diels-Alder reactions using a chiral lanthanide Lewis acid. Enantioselective synthesis of tetrahydroquinoline derivatives using a catalytic amount of a chiral source Haruro Ishitani, Shu̅ Kobayashi Tetrahedron Letters Chemical EngineeringEngineeringCatalytic AmountOrganic ChemistryChiral Source	1996	244
Enantioselective Mannich-Type Reactions Using a Novel Chiral Zirconium Catalyst for the Synthesis of Optically Active β-Amino Acid Derivatives Haruro Ishitani, Masaharu Ueno, Shu̅ Kobayashi Journal of the American Chemical Society	2000	228
Lanthanide Triflate Catalyzed Imino Diels-Alder Reactions; Convenient Syntheses of Pyridine and Quinoline Derivatives Shu̅ Kobayashi, Haruro Ishitani, Satoshi Nagayama Synthesis Chemical EngineeringCross-coupling ReactionEngineeringConvenient SynthesesLanthanide Triflate	1995	225
Lanthanide(III)-Catalyzed Enantioselective Diels-Alder Reactions. Stereoselective Synthesis of Both Enantiomers by Using a Single Chiral Source and a Choice of Achiral Ligands Shu̅ Kobayashi, Haruro Ishitani Journal of the American Chemical Society EngineeringBoth EnantiomersSingle Chiral SourceAltmetric Attention ScoreOrganic Chemistry	1994	207
Catalytic Asymmetric Strecker Synthesis. Preparation of Enantiomerically Pure α-Amino Acid Derivatives from Aldimines and Tributyltin Cyanide or Achiral Aldehydes, Amines, and Hydrogen Cyanide Using a Chiral Zirconium Catalyst Haruro Ishitani, Susumu Komiyama, Yoshiki Hasegawa, Journal of the American Chemical Society α-Amino Acid DerivativesEngineeringNatural SciencesDiversity-oriented SynthesisAchiral Aldehydes	2000	206
Scandium trifluoromethanesulfonate (Sc(OTf)3). A novel reusable catalyst in the Diels-Alder reaction Shu̅ Kobayashi, Iwao Hachiya, Mitsuharu Araki, Tetrahedron Letters Chemical EngineeringNovel Reusable CatalystEngineeringAlkene MetathesisScandium Trifluoromethanesulfonate	1993	193
Catalytic, Enantioselective Synthesis ofα-Aminonitriles with a Novel Zirconium Catalyst Haruro Ishitani, Susumu Komiyama, Shu̅ Kobayashi Angewandte Chemie International Edition	1998	160
A Novel Inhibitor of Ceramide Trafficking from the Endoplasmic Reticulum to the Site of Sphingomyelin Synthesis Satoshi Yasuda, H. Kitagawa, Masaharu Ueno, Journal of Biological Chemistry	2001	152

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