Ogoshi Research GROUP

Ogoshi Research GROUP Research on organotransition metal-catalyzed reactions and the isolation of reaction intermediates. h

https://pubs.acs.org/doi/10.1021/jacs.0c09639Our new paper is available on ASAP生越研の新しい論文がUPされました。
29/10/2020

https://pubs.acs.org/doi/10.1021/jacs.0c09639
Our new paper is available on ASAP
生越研の新しい論文がUPされました。

The first example of the oxidative addition of a C(sp3)–F bond in trifluoromethylarenes to a nickel(0) complex is described. A nickel(0) complex that bears two N-heterocyclic carbene (NHC) ligands of low steric demand is able to cleave C(sp3)–F bonds of trifluoromethylarenes to afford the corres...

CsF-Catalyzed Fluoroacylation of Tetrafluoroethylene Using Acyl Fluorides for the Synthesis of Pentafluoroethyl KetonesN...
29/10/2020

CsF-Catalyzed Fluoroacylation of Tetrafluoroethylene Using Acyl Fluorides for the Synthesis of Pentafluoroethyl Ketones
Naoyoshi Ishida, Hiroaki Iwamoto, Denise Eimi Sunagawa, Masato Ohashi, Sensuke Ogoshi∗

Ni(0)-Catalyzed Synthesis of Polycyclic α,β-Unsaturated γ-Lactams via Intramolecular Carbonylative Cycloaddition of Yne-...
09/10/2020

Ni(0)-Catalyzed Synthesis of Polycyclic α,β-Unsaturated γ-Lactams via Intramolecular Carbonylative Cycloaddition of Yne-imines with CO
K. Ashida, Y. Hoshimoto, S. Ogoshi
Synlett, 2020, eFirst Article
A Ni(0)-catalyzed intramolecular carbonylative cycloaddition between 1,5-yne-imines and carbon monoxide (CO) is disclosed. When Ni(CO)3PCy3 was employed as a pre-catalyst, a variety of polycyclic α,β-unsaturated γ-lactams were prepared in up to 78% yield with 100% atom efficiency. Aza-nickelacycles, generated by the oxidative cyclization of yne-imines on the Ni(0) center, were experimentally confirmed as key intermediates. Moreover, diastereoselective transformations of the obtained products to afford highly substituted polycyclic γ-lactams with three contiguous carbon stereocenters are reported.
Invited Contribution to "Modern Nickel-Catalyzed Reactions"

Thieme E-Books & E-Journals

https://pubs.acs.org/doi/10.1021/acs.orglett.0c03189our new publication is available .
30/09/2020

https://pubs.acs.org/doi/10.1021/acs.orglett.0c03189
our new publication is available .

Trifluorovinylzinc is a common synthetic intermediate for trifluorovinyl derivatives, including α,β,β-trifluorostyrenes and hexafluorobutadiene. Here, we report a novel synthetic approach for the formation of trifluorovinylzinc chloride via a C–F bond activation of tetrafluoroethylene (TFE), wh...

生越研の論文がJACSにアクセプトされました。Rotation-Triggered Transmetalation on Heterobimetallic Cu/Al N-Phosphine-Oxide-Substituted Imidaz...
24/04/2020

生越研の論文がJACSにアクセプトされました。
Rotation-Triggered Transmetalation on Heterobimetallic Cu/Al N-Phosphine-Oxide-Substituted Imidazolylidene Complex

Congratulations Takahiro! 
Our new paper is available.J. Am. Chem. Soc., 2020, JAMs

https://pubs.acs.org/doi/10.1021/jacs.0c03252

24/12/2019

生越研の論文がJACSにアクセプトされました。
Enantioselective Synthesis of Polycyclic γ-Lactams with Multiple Chiral Carbon Centers via Ni(0)-Catalyzed Asymmetric Carbonylative Cycloadditions without Stirring
Congratulations Keita!
https://pubs.acs.org/doi/pdf/10.1021/jacs.9b12493

無撹拌が高収率の鍵。

Dinner with Prof. Walter Leitner( RWTHAACHEN Univ.)after the lecture at our department.
09/11/2019

Dinner with Prof. Walter Leitner( RWTHAACHEN Univ.)
after the lecture at our department.

We are the champion of the volleyball tournament of faculty of engineering.
06/11/2019

We are the champion of the volleyball tournament of faculty of engineering.

27/10/2019

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住所

山田丘2/1
Suita-shi, Osaka
565-0871

ウェブサイト

http://www.chem.eng.osaka-u.ac.jp/~ogoshi-lab/en/index.html

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