TANABE You
Graduating School 【 display / non-display 】
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Graduating School:The University of Tokyo
Faculty:Faculty of Agriculture
Kind of school:University
Date of graduation:1978.03
Completion status:Graduated
Country location code:JAPAN
Graduate School 【 display / non-display 】
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Graduate school:Kyoto University
Course completed:Master's Course
Date of completion:1980.03
Completion status:Completed
Country location code:JAPAN
Degree 【 display / non-display 】
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Degree name:ph.D.
Classified degree field:Synthetic chemistry
Degree awarding institution:Tokyo Institute of Technology
Acquisition way:Thesis
Date of acquisition:1989.12
Campus Career 【 display / non-display 】
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Job function organization:Kwansei Gakuin University School of Science and Technology Department of Chemistry
Career:Associate Professor (as old post name)
Duties period:1991.04 - 1997.03 -
Job function organization:Kwansei Gakuin University School of Science and Technology Department of Chemistry
Career:Professor
Duties period:1997.04 -
External Career 【 display / non-display 】
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Name of affiliation:
Career:Researcher
Periods of career:1980.04 - 1991.03 -
Name of affiliation:
Career:Researcher
Periods of career:1983.04 - 1985.03
Field of expertise (Grants-in-aid for Scientific Research classification) 【 display / non-display 】
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Field of expertise (Grants-in-aid for Scientific Research classification):Synthetic chemistry
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Field of expertise (Grants-in-aid for Scientific Research classification):Organic chemistry
Papers 【 display / non-display 】
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Written language: English
Title of paper: First Total Synthesis of (±)-6'-Methoxyretrojusticidin B Utilizing Regiocontrolled Benzannulation: Structural Inconsistency with Procumphthalide A and Its Revision to 5'-Methoxyretrochinensin.
Publication title: Synlett (p.2275 - 2278)
Date of issue: 2010.09
Name of author(s): Eri Yoshida, Daisuke Yamashita, Ryo Sakai, Yoo Tanabe, Yoshinori NishiiType of publication: Research paper (scientific journal)
Co-author classification: Joint Work
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Written language: English
Title of paper: Mild, Efficient, and Robust Method for Stereocomplementary Iron-catalyzed Cross-coupling using (E)- and (Z)-Enol Tosylates.
Publication title: Synlett (p.2087 - 2091)
Date of issue: 2010.08
Name of author(s): Hiroshi Nishikado, Hidefumi Nakatsuji, Kanako Ueno, Ryohei Nagase, Yoo TanabeType of publication: Research paper (scientific journal)
Co-author classification: Joint Work
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Written language: English
Title of paper: First sequential Mukaiyama–Michael reaction/crossed-Claisen condensation using two molar ketene silyl acetals and one molar α,ß-unsaturated esters promoted by a NaOH catalyst.
Publication title: Chem. Commun. vol.46 (p.5930 - 5932)
Date of issue: 2010.07
Name of author(s): Hiroaki Tamagaki, Yuuya Nawate, Ryohei Nagase, Yoo TanabeType of publication: Research paper (scientific journal)
Co-author classification: Joint Work
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Written language: English
Title of paper: Pentafluorophenylammonium Trifluoromethanesulfonimide: Mild, Powerful, and Robust Catalyst for Mukaiyama Aldol and Mannich Reactions between Ketene Silyl Acetals and Ketones or Oxime Ethers.
Publication title: Adv. Synth. Catal. vol.352 (p.1128 - 1134)
Date of issue: 2010.03
Name of author(s): Ryohei Nagase, Jun Osada, Hiroaki Tamagaki, Yoo TanabeType of publication: Research paper (scientific journal)
Co-author classification: Joint Work
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Written language: English
Title of paper: General, Robust, and Stereocomplementary Preparation of a,b-Disubstituted a,b-Unsaturated Esters.
Publication title: Org. Lett. vol.11 (p.4258 - 4261)
Date of issue: 2009.09
Name of author(s): Hidefumi Nakatsuji, Hiroshi Nishikado, Kanako Ueno, Yoo TanabeType of publication: Research paper (scientific journal)
Co-author classification: Joint Work
Grant-in-Aid for Scientific Research 【 display / non-display 】
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Research item:Grant-in-Aid for Scientific Research(C)
Research activities period:2018.04 - 2021.03
Presentations 【 display / non-display 】
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Presentation (Written) language: English
Conference Name: The 2nd International Symposium on Process Chemistry
Conference classification: International conference
Meeting period: 2011.08
Topic / Session title: General, robust, and stereocomplementary preparation of multi-substituted α,β-unsaturated esters utilizing successive enol tosylations (phosphorylations) of β-ketoesters and various cross-couplings
Form of presentation: Oral Presentation(general)
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Presentation (Written) language: English
Conference Name: 2010 International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010)
Conference classification: International conference
Meeting period: 2010.12
Topic / Session title: Construction of three consective asymmetric centers utilizing Ti-Claisen-Aldol domino reaction
Form of presentation: Oral Presentation(general)
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Presentation (Written) language: English
Conference Name: 2010 International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010)
Conference classification: International conference
Meeting period: 2010.12
Topic / Session title: First sequential Mukaiyama–Michael reaction/crossed-Claisen condensation using two molar ketene silyl acetals and one molar α,β-unsaturated esters promoted by a NaOH catalyst
Form of presentation: Oral Presentation(general)
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Presentation (Written) language: English
Conference Name: 2010 International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010)
Conference classification: International conference
Meeting period: 2010.12
Topic / Session title: Stereocomplementary preparation for trisubstituted (E)- and (Z)-α,β-unsaturated esters utilizing successive enol tosylations and Fe-catalyzed cross couplings of β-ketoesters and α-formylesters
Form of presentation: Oral Presentation(general)
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Presentation (Written) language: English
Conference Name: 2010 International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010)
Conference classification: International conference
Meeting period: 2010.12
Topic / Session title: Highly stereocomplementary method for the preparation of (E)- and (Z)-α,β-substituted unsaturated esters utilizing stereoretentive reduction of (E)- and (Z)-stereodefined enol
Form of presentation: Oral Presentation(general)