Masahito Segi - Concepedia

Author

Masahito Segi

Kanazawa University ORCID

Also Known As

M. SEGI, M. Segi, Masahito SEGI, Masahito Segi, Masahito. Segi, Segi, M., Segi, Masahito

244

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Kanazawa University The University of Osaka Japan Science and Technology Agency Texas A&M University

About

Masahito Segi is an author at Kanazawa University specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	19	35	868
2	Biomolecular Engineering	12	18	404
3	Natural Sciences	9	9	290
4	Biochemistry	6	6	182
5	Arts	1	1	70

Masahito Segi

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Direct conversion of aldehydes to seleno- and thioaldehydes Masahito Segi, Tadashi Nakajima, Sohei Suga, Journal of the American Chemical Society Direct ConversionBioorganic ChemistryEngineeringChemical AnalysisDonut Icon	1988	104
Synthesis and Structure of Telluroamides and Selenoamides. The First Crystallographic Study of Telluroamides Guangming Li, Ralph A. Zingaro, Masahito Segi, Organometallics Combinatorial ChemistryCrystal StructureDiversity Oriented SynthesisFirst Successful SynthesisEngineering	1997	76
Telluro aldehydes and telluro ketones Masahito Segi, Tadashi Koyama, Yukihiro Takata, Journal of the American Chemical Society AltmetricsAldehyde DehydrogenaseDonut IconInformationDatabases	1989	70
Catalytic Cu(I) assisted polyfunctionalization of zirconacyclopentenes Bruce H. Lipshutz, Masahito Segi Tetrahedron Catalytic CuOrganometallic CatalysisCatalysisChemistryCatalytic Synthesis	1995	56
An efficient construction of a selenocarbonyl unit by the reaction of acetal derivatives with bis(dimethylaluminum) selenide Masahito Segi, T. Takahashi, Hiroyuki Ichinose, Tetrahedron Letters Asymmetric CatalysisChemical EngineeringNovel OrganocatalystsEngineeringSelenocarbonyl Unit	1992	56
Novel route to selenoketones from ketones by the use of bis(dimethylaluminum) selenide Masahito Segi, Tadashi Koyama, Tadashi Nakajima, Tetrahedron Letters BiochemistryNatural SciencesNovel RouteOrganic ChemistryChemistry	1989	51
α,β-Unsaturated selenoaldehydes and selenoketones the reaction behavior as a heterodiene and/or a dienophile Guangming Li, Masahito Segi, Tadashi Nakajima Tetrahedron Letters β-Unsaturated SelenoaldehydesBiosynthesisBioorganic ChemistryEngineeringBiochemistry	1992	42
A Facile Synthesis of Seleno- and Telluroformamides Masahito Segi, Akihiro Kojima, Tadashi Nakajima, Synlett Combinatorial ChemistryEngineeringN-disubstituted FormamidesCorresponding SelenoformamidesFacile Synthesis	1991	40
Intramolecular Diels-Alder reaction of selenoaldehydes Masahito Segi, Mamoru Takahashi, Tadashi Nakajima, Tetrahedron Letters Organic ChemistryIntramolecular Diels-alder ReactionDeoxygenationBiochemistry	1988	37
[4 + 2] Dimerization and Cycloaddition Reactions of α,β-Unsaturated Selenoaldehydes and Selenoketones Guangming Li, Shuqiang Niu, Masahito Segi, The Journal of Organic Chemistry	1999	35

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