Taro Nonomura - Concepedia

Author

Taro Nonomura

The University of Tokyo

Also Known As

T. NONOMURA, TARO NONOMURA, Taro Nonomura

Publications

874

Citations

H-Index

Concepts

All Affiliations

The University of Tokyo Tohoku University Nagoya City University

About

Taro Nonomura is an author at The University of Tokyo specializing in natural sciences, chemistry, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	6	6	263
2	Engineering	3	3	88
3	Medicine	3	3	181
4	Allergy	1	1	74
5	Allergy Medicine	1	1	74

Taro Nonomura

Publications

800

Citations

H-Index

Page 1

	Year	Citations
The Complete Structure of Maitotoxin, Part I: Configuration of the C1C14 Side Chain Makoto Sasaki, Nobuaki Matsumori, Takahiro Maruyama, Angewandte Chemie International Edition in English	1996	111
The Complete Structure of Maitotoxin, Part II: Configuration of the C135C142 Side Chain and Absolute Configuration of the Entire Molecule Taro Nonomura, Makoto Sasaki, Nobuaki Matsumori, Angewandte Chemie International Edition in English	1996	109
Synthesis and Evaluation of Lysophosphatidylserine Analogues as Inducers of Mast Cell Degranulation. Potent Activities of Lysophosphatidylthreonine and Its 2-Deoxy Derivative Masazumi Iwashita, Kumiko Makide, Taro Nonomura, Journal of Medicinal Chemistry Allergy MedicineMast Cell DisorderImmunologyAllergenMast Cell Degranulation	2009	74
A Novel Hemiporphyrazine Comprising Three Isoindolediimine and Three Thiadiazole Units Nagao Kobayashi, Sayaka Inagaki, Victor N. Nemykin, Angewandte Chemie International Edition Metal IonsPharmaceutical ScienceOrganic ChemistryPharmacotherapyChemistry	2001	60
Synthesis and stereochemical confirmation of the cis-fused L/M and N/O ring systems of maitotoxin Makoto Sasaki, Taro Nonomura, Michio Murata, Tetrahedron Letters Stereochemical ConfirmationBioorganic ChemistryHeterocyclicBiochemistryNatural Sciences	1994	58
Long-range carbon-proton coupling constants for stereochemical assignment of acyclic structures in natural products: Configuration of the C5C9 portion of maitotoxin Nobuaki Matsumori, Taro Nonomura, Makoto Sasaki, Tetrahedron Letters	1996	54
Synthetic approach toward complete structure determination of maitotoxin. stereochemical assignment of the C63-C68 acyclic linkage Makoto Sasaki, Taro Nonomura, Michio Murata, Tetrahedron Letters Microbial ToxinMedicinal ChemistryToxinologyBiochemistryNatural Sciences	1995	47
Design, synthesis, and BK channel-opening activity of hexahydrodibenzazepinone derivatives Toshihiko Tashima, Yoshimi Toriumi, Yumi Mochizuki, Bioorganic & Medicinal Chemistry HeterocyclicBk Channel-opening ActivityOrganic ChemistryChemistryHeterocycle Chemistry	2006	45
Synthesis and reactions of optically pure cyclohexyl(<i>o</i>‐methoxyphenyl)phosphine‐borane and <i>t</i>‐butyl‐(<i>o</i>‐methoxyphenyl)phosphine‐borane Tsuneo Imamoto, Masatoshi Matsuo, Taro Nonomura, Heteroatom Chemistry EngineeringBorane‐thf ComplexNatural SciencesDiversity-oriented SynthesisPure Phosphine‐boranes	1993	43
Dehydroabietic acid derivatives as a novel scaffold for large-Conductance calcium-Activated K+ channel openers Tomohiko Ohwada, Taro Nonomura, Keisuke Maki, Bioorganic & Medicinal Chemistry Letters Hyperpolarization (Biology)Dehydroabietic Acid DerivativesIon ChannelsNovel ScaffoldElectrophysiology	2003	41

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