Shoichiro Uyeo - Concepedia

Author

Shoichiro Uyeo

Shionogi (Japan)

Also Known As

SHOICHIRO UYEO, Shoichiro UYEO, Shoichiro Uyeo

Publications

504

Citations

H-Index

Concepts

All Affiliations

Shionogi (Japan)Kyoto University

About

Shoichiro Uyeo is an author at Shionogi (Japan) specializing in pharmacology, organic chemistry, and biomolecular engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biomolecular Engineering	9	9	216
2	Biochemistry	8	8	151
3	Natural Sciences	7	7	146
4	Engineering	6	6	178
5	Medicine	6	6	108

Shoichiro Uyeo

Publications

395

Citations

H-Index

Page 1

	Year	Citations
Total synthesis of lupeol Gilbert Stork, Shoichiro Uyeo, T. Wakamatsu, Journal of the American Chemical Society Molecular SciencesEngineeringChemical MeasurementChemical AnalysisDonut Icon	1971	64
Stereocontrolled, straightforward synthesis of 3-substituted methyl 7α-methoxy-1-oxacephems M. YOSHIOKA, Teruji Tsuji, Shoichiro Uyeo, Tetrahedron Letters Organic ChemistryStereoselective SynthesisChemistry3-Substituted Methyl 7α-Methoxy-1-oxacephemsSynthetic Chemistry	1980	43
Synthetic studies on β-lactam antibiotics. Part 16. synthesis of 1-carba-2-penem-3-carboxylic acid esters from penicillins utilizing a carbon-carbon coupling reaction Hiroshi Onoue, Masayuki Narisada, Shoichiro Uyeo, Tetrahedron Letters Medicinal ChemistryEngineeringβ-Lactam AntibioticsCarbon-carbon Coupling ReactionSynthetic Studies	1979	32
Pachysandra Alkaloids. VIII. Structures of Pachystermine-A and -B, Novel Type Alkaloids Having a β-Lactam Ring Tohru Kikuchi, Shoichiro Uyeo Chemical and Pharmaceutical Bulletin Pachysandra AlkaloidsBioorganic ChemistryBiochemistryβ-Lactam RingMedicine	1967	31
Reduction and Reductive Alkylation of α-<u>tert</u>-Butylthio Carbonyl Compounds. An Efficient Method for Stepwise α-Alkylation of Esters, Nitriles and Ketones Via the α-<u>Tert</u>-Butylthio Derivatives S. Kamata, Shoichiro Uyeo, N. HAGA, Synthetic Communications Reductive AlkylationChemical EngineeringEnantioselective SynthesisDerivativesApplicable Method	1973	27
A simple and stereocontrolled syntheses of a 1β-methylcarbapenem key intermediate by means of organosilicon chemistry Shoichiro Uyeo, H. ITANI Tetrahedron Letters EngineeringBiochemistryNatural Sciences1β-Methylcarbapenem Key IntermediateOrganic Chemistry	1991	25
Synthetic studies on .beta.-lactam antibiotics. 12. Stereocontrolled synthesis of 7.alpha.-methoxy-1-oxacephems from 6-epipenicillin G Shoichiro Uyeo, Ikuo Kikkawa, Yoshio Hamashima, Journal of the American Chemical Society Medicinal ChemistryAntimicrobial Drug DiscoveryBioorganic ChemistryPharmaceutical ChemistryBiochemistry	1979	22
Studies on the alkaloids of pachysandra terminalis sieb. et zucc. (6). :structure of pachystermine - a and -b, novel type alkaloids having β-lactam ring system. Tohru Kikuchi, Shoichiro Uyeo Tetrahedron Letters β-Lactam Ring SystemBiochemistryNovel Type AlkaloidsPachysandra Terminalis SiebPharmacology	1965	21
Synthesis of 1-carbacephem derivatives. Shoichiro Uyeo, H. Ona Chemical and Pharmaceutical Bulletin 1-Carbacephem DerivativesBioorganic ChemistryDerivativesMedicineHighest Antibacterial Activity	1980	20
Synthetic studies on isoquinoline alkaloids. II. Selective conversion of 3,9,10-substituted tetrahydroprotoberberines into 3,9,10-substituted 5,6,7,8,13,14-hexahydrodibenz(c,g)azecines. Wataru Nagata, Kyo Okada, Hiroshi Itazaki, Chemical and Pharmaceutical Bulletin Combinatorial ChemistryPhenolic FunctionSophisticated Total SynthesisEngineeringBiochemistry	1975	16

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