Tamotsu Fujisawa - Concepedia

Author

Tamotsu Fujisawa

Also Known As

T Fujisawa, T. FUJISAWA, T. Fujisawa, TAMOTSU FUJISAWA, Tamotsu FUJISAWA, Tamotsu Fujisawa, Taro Fujisawa, Tatsuji Fujisawa

432

Publications

4.9K

Citations

H-Index

Concepts

All Affiliations

Mie University Sagami Chemical Research Institute

About

Tamotsu Fujisawa is an author at Mie University specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	32	128	3.5K
2	Natural Sciences	24	54	1.5K
3	Biochemistry	21	40	1.1K
4	Medicine	2	2	42
5	Arts	1	1	10

Tamotsu Fujisawa

167

Publications

4.5K

Citations

H-Index

Page 1

	Year	Citations
Enantiospecific synthesis of optically pure (3s)-hydroxy esters by the stereocontrolled yeast reduction of α-sulfenyl-β-ketoesters Tamotsu Fujisawa, Toshiyuki Itoh, Toshio Sato Tetrahedron Letters EngineeringYeast ReductionOrganic ChemistryEnantiospecific SynthesisStereoselective Synthesis	1984	80
Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate Tamotsu Fujisawa, Yuuji Kooriyama, Makoto Shimizu Tetrahedron Letters Asymmetric CatalysisEngineeringOrganic ChemistryEster EnolateCatalysis	1996	75
Regioselective Conversion of Epoxides to Halohydrins by Titanium(IV) Halide-Lithium Halide Complex Makoto Shimizu, Akifumi Yoshida, Tamotsu Fujisawa Synlett Chemical EngineeringRegioselective ConversionEngineeringAlkene Metathesis2,3-Epoxy Alcohols	1992	74
(<i>S</i>)-β,ω-Dihydroxyalkyl Phenyl Sulfones. Synthesis by Bakers Yeast Reduction and Use as Precursors of Optically Active Lactones Toshio Sato, Yoshiyuki Okumura, Junichi Itai, Chemistry Letters EngineeringBiochemistryBakers Yeast ReductionNatural SciencesOptically Active Lactones	1988	71
Optically pure (s)-3-phenylthio-1,2-propanediol: synthesis by the yeast reduction and use as a precursor of both enantiomers of secondary alcohols Tamotsu Fujisawa, Toshiyuki Itoh, Mikio Nakai, Tetrahedron Letters Bioorganic ChemistryNatural SciencesYeast ReductionOrganic ChemistryStereoselective Synthesis	1985	67
Diastereoface Discrimination in the Addition of Acetylide to a Chiral Aldehyde, Leading to a Synthesis of (+)-Deoxybiotin in Enantiomerically Pure Form Starting from L-Cysteine Tamotsu Fujisawa, Michiharu Nagai, Yoshihiro Koike, The Journal of Organic Chemistry Bioorganic ChemistryEngineeringAltmetric Attention ScoreOrganic ChemistryChemistry	1994	67
FACILE SYNTHESIS OF BENZYL KETONES BY THE REDUCTIVE COUPLING OF BENZYL BROMIDE AND ACYL CHLORIDES IN THE PRESENCE OF A PALLADIUM CATALYST AND ZINC POWDER Toshio Sato, Kouichi Naruse, Masashi Enokiya, Chemistry Letters Chemical EngineeringCross-coupling ReactionEngineeringBenzyl BromideOrganic Chemistry	1981	66
Asymmetric reduction of α,β-unsaturated ketones with chiral hydride reagents prepared from lithium aluminum hydride and (S)-4-anilino- and (S)-4-(2,6-xylidino)-3-methylamino-1-butanol Toshio Sato, Yoshihiko Gotoh, Yasutaka Wakabayashi, Tetrahedron Letters Chiral Hydride ReagentsChemical EngineeringEngineeringOrganic ChemistryCatalysis	1983	65
Selective synthesis of optically active 3-haloazetidin-2-ones or aziridines by the condensation of various metal enolates of α-haloacetate with a chiral imine Tamotsu Fujisawa, Ryuuichirou Hayakawa, Makoto Shimizu Tetrahedron Letters Active 3-Haloazetidin-2-onesChiral ImineOrganic ChemistryStereoselective SynthesisChemistry	1992	60
Stereocontrol in the reduction of 1,2-diimine with an oxazaborolidine catalyst. Highly stereoselective preparation of (R,R)-1,2-diphenylethylenediamine Makoto Shimizu, Mie Kamei, Tamotsu Fujisawa Tetrahedron Letters Oxazaborolidine CatalystHighly Stereoselective PreparationChemical EngineeringEngineeringOrganic Chemistry	1995	59

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