Saito Group (@saitogroup) 's Twitter Profile
Saito Group

@saitogroup

Young research group at Ludwig Maximilian University in Munich, Germany. ミュンヘン大学 齋藤研究室. We make and use sulfur functionalities. 現在の主な研究内容: 硫黄官能基の合成と利用。

ID: 1565784408661131265

linkhttps://www.saitolab.de calendar_today02-09-2022 19:31:22

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303 Followers

159 Following

Angewandte Chemie (@angew_chem) 's Twitter Profile Photo

Synthesis of S(IV)-Stereogenic Chiral Thio-Oxazolidinones via Palladium-Catalyzed Asymmetric [3+2] Annulations (Liang-Qiu Lu and co-workers) onlinelibrary.wiley.com/doi/10.1002/an…

Angewandte Chemie (@angew_chem) 's Twitter Profile Photo

Phosphorane-Promoted C-C Coupling during Aryne Annulations (Thomas R. Hoye and co-workers) #openaccess #AngewandteVIP onlinelibrary.wiley.com/doi/10.1002/an…

Saito Group (@saitogroup) 's Twitter Profile Photo

#日本化学会年会 で発表します。 セッション日時: 2024年3月18日(月) 15:55 ~ 16:15 講演番号: E1123-1vn-01 演題: ワンポット3成分反応による硫黄官能基の合成 (One-Pot, Three-Component Assembly of Sulfur Functionalities)

Saito Group (@saitogroup) 's Twitter Profile Photo

A new preprint from our group posted on ChemRxiv Enantioselective Synthesis of Sulfinamidines via Asymmetric Nitrogen Transfer from N-H Oxaziridines to Sulfenamides go.shr.lc/43fDmZQ

A new preprint from our group posted on <a href="/ChemRxiv/">ChemRxiv</a> 

Enantioselective Synthesis of Sulfinamidines via Asymmetric Nitrogen Transfer from N-H Oxaziridines to Sulfenamides

go.shr.lc/43fDmZQ
Angewandte Chemie (@angew_chem) 's Twitter Profile Photo

N-Heteroaromatic Fluoroalkylation through Ligand Coupling Reaction of Sulfones (Jinbo Hu and co-workers) ShanghaiTech University onlinelibrary.wiley.com/doi/10.1002/an…

Arka Porey (@poreyarka) 's Twitter Profile Photo

Happy to share our recent work on acridine catalyzed direct decarboxylative thiolation from carboxylic acid and elemental sulfur. pubs.acs.org/doi/10.1021/ac…

Saito Group (@saitogroup) 's Twitter Profile Photo

Thank you Johannes @TeichertLab for visiting Universität München and giving a great lecture on stable neutral homoaromatic hydrocarbons in our OC Kolloquium.

Thank you Johannes @TeichertLab for visiting <a href="/LMU_Muenchen/">Universität München</a> and giving a great lecture on stable neutral homoaromatic hydrocarbons in our OC Kolloquium.
Saito Group (@saitogroup) 's Twitter Profile Photo

Many thanks Matthieu @SollogoubM for visiting us Universität München and giving a wonderful talk about cyclodextrins for catalysis, self-assembly and molecular motors.

J. Am. Chem. Soc. (@j_a_c_s) 's Twitter Profile Photo

Catalytic Asymmetric Synthesis of Sulfinamides via Cu-Catalyzed Asymmetric Addition of Aryl Boroxines to Sulfinylamines | Journal of the American Chemical Society Total Synthesis and Methodology Highlights Boron-Chem-Research #Catalysis #Sulfinamides #Cu #Boroxines pubs.acs.org/doi/10.1021/ja…

Angewandte Chemie (@angew_chem) 's Twitter Profile Photo

Enantioselective Synthesis of Sulfinamidines via Asymmetric Nitrogen Transfer from N-H Oxaziridines to Sulfenamides (Marc Fimm and Fumito Saito) Saito Group #openaccess onlinelibrary.wiley.com/doi/10.1002/an…

J. Am. Chem. Soc. (@j_a_c_s) 's Twitter Profile Photo

Asymmetric 2,3-Addition of Sulfinylamines with Arylboronic Acids Enabled by Nickel Catalysis | Journal of the American Chemical Society Total Synthesis and Methodology Highlights #Sulfinylamines #Arylboronic #Ni #Catalysis pubs.acs.org/doi/10.1021/ja…

J. Am. Chem. Soc. (@j_a_c_s) 's Twitter Profile Photo

Palladium-Catalyzed Addition of Aryl Halides to N-Sulfinylamines for the Synthesis of Sulfinamides | Journal of the American Chemical Society Total Synthesis and Methodology Highlights University of Oxford @RhPdCu Oxford Chemistry #Pd #Catalysis #Arylhalide #Sulfinylamines #Sulfinamides pubs.acs.org/doi/10.1021/ja…

Saito Group (@saitogroup) 's Twitter Profile Photo

Thank you David @barber_daveM for visiting Universität München and give a OC Kolloquium lecture “Sustainability and Scaffold Hopping in Crop ProtecIon Research”. With his interactive lecture style, there were more questions than usual (especially by students).

Thank you David @barber_daveM for visiting <a href="/LMU_Muenchen/">Universität München</a> and give a OC Kolloquium lecture “Sustainability and Scaffold Hopping in Crop ProtecIon Research”. With his interactive lecture style, there were more questions than usual (especially by students).
Saito Group (@saitogroup) 's Twitter Profile Photo

In the last OC colloquium this semester, we enjoyed a talk by Prof. Isabelle Chatainger Isabelle Chataigner about “dearomatization of electron-poor arenes by cycloadditions”. Dr. Sami Lakhdar Sami Lakhdar gave a great lecture about “Making and Breaking Chemical Bonds with Visible light”.

In the last OC colloquium this semester, we enjoyed a talk by Prof. Isabelle Chatainger <a href="/ichataig/">Isabelle Chataigner</a> about “dearomatization of electron-poor arenes by cycloadditions”.  Dr. Sami Lakhdar <a href="/samilakhdar1/">Sami Lakhdar</a> gave a great lecture about “Making and Breaking Chemical Bonds with Visible light”.
Organic Chemistry Portal (@organic_portal) 's Twitter Profile Photo

organic-chemistry.org/abstracts/lit9… A one-pot, three-component synthesis of sulfides uses a sulfoxide reagent as a formal sulfur dication equivalent.

organic-chemistry.org/abstracts/lit9…
A one-pot, three-component synthesis of sulfides uses a sulfoxide reagent as a formal sulfur dication equivalent.
Yoichi Hoshimoto 星本陽一 (@yhoshimoto) 's Twitter Profile Photo

Enjoyed a nice dinner with Fumito Saito Group ‼️ Significantly stimulated by his excellent fighting spirit. ドイツで戦う若手日本人化学者, 斎藤さんとディナー. やはり国外で奮闘するPIと語る時間は刺激的だな. いよいよ明日, LMU Munichへ乗り込みます.

Enjoyed a nice dinner with Fumito <a href="/SaitoGroup/">Saito Group</a> ‼️ Significantly stimulated by his excellent fighting spirit. 
ドイツで戦う若手日本人化学者, 斎藤さんとディナー. やはり国外で奮闘するPIと語る時間は刺激的だな. 

いよいよ明日, LMU Munichへ乗り込みます.
G. Berionni Group (@dr_berionni) 's Twitter Profile Photo

It was a real pleasure to give a lecture at the "Organisch-Chemischen Kolloquium" today at LMU Munich University Universität München. Thanks Saito Group for the invitation and wonderful discussions with Ofial_Lab and all researchers from the chemistry department.

It was a real pleasure to give a lecture at the "Organisch-Chemischen Kolloquium" today at LMU Munich University <a href="/LMU_Muenchen/">Universität München</a>. Thanks <a href="/SaitoGroup/">Saito Group</a> for the invitation and wonderful discussions with <a href="/OfialLab/">Ofial_Lab</a> and all researchers from the chemistry department.