Kengo Miyata - Concepedia

Author

Kengo Miyata

Nagoya University

Also Known As

Kengo MIYATA, Kengo Miyata

Publications

354

Citations

H-Index

Concepts

All Affiliations

Nagoya University

About

Kengo Miyata is an author at Nagoya University specializing in natural sciences, organic chemistry, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	4	4	100
2	Biochemistry	4	4	141
3	Engineering	3	3	90
4	Biomolecular Engineering	3	3	70
5	Medicine	1	1	10

Kengo Miyata

Publications

324

Citations

H-Index

Page 1

	Year	Citations
A Chiral Bidentate sp<sup>2</sup>‐N Ligand, Naph‐diPIM: Application to CpRu‐Catalyzed Asymmetric Dehydrative C‐, N‐, and O‐Allylation Kengo Miyata, H. Kutsuna, Sho Kawakami, Angewandte Chemie International Edition	2011	96
Synthesis and σ receptor affinity of regioisomeric spirocyclic furopyridines Kengo Miyata, Dirk Schepmann, Bernhard Wünsch European Journal of Medicinal Chemistry PharmacologyHeterocycle ChemistryRegioisomeric Spirocyclic FuropyridinesBiochemistry	2014	75
CpRu-catalyzed asymmetric dehydrative allylation Masato Kitamura, Kengo Miyata, Tomoaki Seki, Pure and Applied Chemistry Asymmetric Tsuji–trost AllylationCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented Synthesis	2013	34
Asymmetric Dehydrative C-, N-, and O-Allylation Using Naph-diPIM-dioxo-i-Pr-CpRu/p-TsOH Combined Catalyst Masato Kitamura, Kengo Miyata Synthesis Chemical EngineeringAsymmetric Dehydrative C-EngineeringCross-coupling ReactionBiochemistry	2012	30
A Chiral Bidentate sp<sup>2</sup>‐N Ligand, Naph‐diPIM: Application to CpRu‐Catalyzed Asymmetric Dehydrative C‐, N‐, and O‐Allylation Kengo Miyata, H. Kutsuna, Sho Kawakami, Angewandte Chemie Cross-coupling ReactionEngineeringHeterocyclicBiochemistryNatural Sciences	2011	26
Metabolic Profile of FYX-051 (4-(5-Pyridin-4-yl-1H-[1,2,4]triazol-3-yl)pyridine-2-carbonitrile) in the Rat, Dog, Monkey, and Human: Identification of N-Glucuronides and N-Glucosides Takashi Nakazawa, Kengo Miyata, Koichi Omura, Drug Metabolism and Disposition	2006	24
Ideal pharmacokinetic profile of dotinurad as a selective urate reabsorption inhibitor Koichi Omura, Kengo Miyata, Seiichi Kobashi, Drug Metabolism and Pharmacokinetics	2020	19
(9<i>H</i>‐Fluoren‐9‐yl)methanesulfonyl (Fms): An Amino Protecting Group Complementary to Fmoc Yoshitaka Ishibashi, Kengo Miyata, Masato Kitamura European Journal of Organic Chemistry Bioorganic ChemistryBiochemistryFmoc PgNatural SciencesDiversity-oriented Synthesis	2010	10
Identification of Human UDP-Glucuronosyltransferase and Sulfotransferase as Responsible for the Metabolism of Dotinurad, a Novel Selective Urate Reabsorption Inhibitor Koichi Omura, Keisuke Motoki, Seiichi Kobashi, Drug Metabolism and Disposition	2021	10

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