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Dive into the research topics where Noriyuki Yagi is active.

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Featured researches published by Noriyuki Yagi.


Tetrahedron Letters | 1980

1,6-Dihydro-3 (2H)-pyridinones as synthetic intermediates. Formal synthesis of (±)-tabersonine and (±)-catharanthine

Takeshi Imanishi; Hiroaki Shin; Noriyuki Yagi; Miyoji Hanaoka

Abstract Formal synthesis of (±)-tabersonine (3) and (±)-catharanthine (4) has been achieved starting from ethyl 1,6-dihydro-3 (2H)-pyridinone-1-carboxylate (1a) as a common synthon.


Tetrahedron Letters | 1981

1,6-dihydro-3(2H)-pyridinones as synthetic intermediates. Total synthesis of (±)-tecomanine

Takeshi Imanishi; Noriyuki Yagi; Miyoji Hanaoka

Abstract The first and stereoselective total synthesis of (±)-tecomanine ( 1 ) has been achieved from ethyl 1,6-dihydro-3(2 H )-pyridinone-1-carboxylate ( 2 ) as a synthon.


Tetrahedron Letters | 1981

1,6-dihydro-3(2H)-pyridinones as synthetic intermediates. A novel total synthesis of (±)-ibogamine and (±)-epiibogamine

Takeshi Imanishi; Noriyuki Yagi; Hiroaki Shin; Miyoji Hanaoka

A new synthesis of (±)-ibogamine (4) and (±)-epiibogamine (5), involving the intramolecular Michael addition of the keto unsaturated ester (11), is described.


Archive | 1984

6-Fluoro-1, 4-dihydro-4-oxo-7-substituted piperazinylquinoline-3-carboxylic acids and the method for preparing the same

Yasuo Itoh; Hideo Kato; Nobuo Ogawa; Eiichi Koshinaka; Tomio Suzuki; Noriyuki Yagi


Chemical & Pharmaceutical Bulletin | 1990

Studies on Antiallergic Agents. I. : Synthesis and Antiallergic Activity of Novel Pyrazine Derivatives

Eiichi Makino; Nobuhiko Iwasaki; Noriyuki Yagi; Tetsuo Ohashi; Hideo Kato; Yasuo Ito; Hiroshi Azuma


Chemical & Pharmaceutical Bulletin | 1985

1,6-Dihydro-3(2H)-pyridinones. X. 2-Azabicyclo(2.2.2)octane ring formation via intramolecular Michael reaction: Total synthesis of (.+-.)-ibogamine and (.+-.)-epiibogamine.

Takeshi Imanishi; Noriyuki Yagi; Miyoji Hanaoka


Chemical & Pharmaceutical Bulletin | 1981

1,6-Dihydro-3 (2H)-pyridinones as Synthetic Intermediates. A Convenient Total Synthesis of (±)-Cleavamine

Takeshi Imanishi; Akira Nakai; Noriyuki Yagi; Miyoji Hanaoka


Chemical & Pharmaceutical Bulletin | 1983

1, 6-Dihydro-3 (2H)-pyridinones. VII. Stereoselective Total Synthesis of a Monoterpene Alkaloid, (±)-Tecomanine

Takeshi Imanishi; Noriyuki Yagi; Miyoji Hanaoka


Archive | 1984

A 6-fluoro-1,4-dihydro-4-oxo-7-substituted piperazinyl-quinoline-3-carboxylic acid derivative and the method for preparing the same

Yasuo Itoh; Hideo Kato; Nobuo Ogawa; Eiichi Koshinaka; Tomio Suzuki; Noriyuki Yagi


Chemical & Pharmaceutical Bulletin | 1983

1, 6-Dihydro-3 (2H)-pyridinones. IV. Synthesis of (±)-Tabersonine and (±)-Cleavamine via a Common Intermediate, Ethyl 3-Ethyl-3-hydroxy-1, 2, 3, 6-tetrahydropyridine-1-carboxylate

Takeshi Imanishi; Hiroaki Shin; Noriyuki Yagi; Akira Nakai; Miyoji Hanaoka

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Nobuhiko Iwasaki

Tokyo Medical and Dental University

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