Takeshi Yasui - Concepedia

Author

Takeshi Yasui

Nagoya University ORCID

Also Known As

Hirotaka Uchida, T Yasui, T. Yasui, TAKESHI YASUI, Takeshi YASUI, Takeshi Yasui, Yasui, T., Yasui, Takeshi

134

Publications

Citations

H-Index

Concepts

All Affiliations

Nagoya University Japan Science and Technology Agency Western Region Agricultural Research Center Kumamoto University Ministry of Agriculture Forestry and Fisheries

About

Takeshi Yasui is an author at Nagoya University specializing in engineering, chemistry, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	15	18	2.1K
2	Natural Sciences	8	8	631
3	Biochemistry	6	6	816
4	Medicine	5	5	377
5	Biology	1	1	14

Takeshi Yasui

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Enantioselective Kita Oxidative Spirolactonization Catalyzed by In Situ Generated Chiral Hypervalent Iodine(III) Species Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara Angewandte Chemie International Edition	2010	457
Quaternary Ammonium (Hypo)iodite Catalysis for Enantioselective Oxidative Cycloetherification Muhammet Uyanik, H. Okamoto, Takeshi Yasui, Science EngineeringCatalytic UseHeterocyclicHydrogen PeroxideHypervalent Iodine Compounds	2010	414
In Situ Generated (Hypo)Iodite Catalysts for the Direct α‐Oxyacylation of Carbonyl Compounds with Carboxylic Acids Muhammet Uyanik, Daisuke Suzuki, Takeshi Yasui, Angewandte Chemie International Edition Carbonyl CompoundsChemical EngineeringEngineeringBiochemistryIndustrial Catalysis	2011	340
Genetic elimination of a starch granule protein, SGP-1, of wheat generates an altered starch with apparent high amylose Makoto Yamamori, Shuzo Fujita, K Hayakawa, Theoretical and Applied Genetics Plant GeneticsEngineeringBiochemistryGeneticsStarch Granule Protein	2000	254
Hydrogen Bonding and Alcohol Effects in Asymmetric Hypervalent Iodine Catalysis: Enantioselective Oxidative Dearomatization of Phenols Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara Angewandte Chemie International Edition Additional Achiral AlcoholsChemical EngineeringEngineeringIodine ChoosesEnantioselective Oxidative Dearomatization	2013	234
Chiral hypervalent iodine-catalyzed enantioselective oxidative Kita spirolactonization of 1-naphthol derivatives and one-pot diastereo-selective oxidation to epoxyspirolactones Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara Tetrahedron EngineeringOrganic ChemistryCatalysisStereoselective SynthesisChemistry	2010	192
Enantioselective Kita Oxidative Spirolactonization Catalyzed by In Situ Generated Chiral Hypervalent Iodine(III) Species Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara Angewandte Chemie Mit IodEngineeringInformationChemometricsOrganic Chemistry	2010	154
Chiral Hypervalent Organoiodine-Catalyzed Enantioselective Oxidative Spirolactonization of Naphthol Derivatives Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara The Journal of Organic Chemistry Novel OrganocatalystsEngineeringNatural SciencesDiversity-oriented SynthesisOrganic Chemistry	2017	82
In Situ Generated (Hypo)Iodite Catalysts for the Direct α‐Oxyacylation of Carbonyl Compounds with Carboxylic Acids Muhammet Uyanik, Daisuke Suzuki, Takeshi Yasui, Angewandte Chemie EngineeringChemical AnalysisSowohl H2o2 AlsIodite CatalystsOrganic Chemistry	2011	79
Hypervalent iodine-catalyzed oxylactonization of ketocarboxylic acids to ketolactones Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara Bioorganic & Medicinal Chemistry Letters EngineeringOrganic ChemistryHypervalent Iodine-catalyzed OxylactonizationCatalysisChemistry	2009	75

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