There was an issue where the figures in the review were not displayed, but this has now been resolved after we uploaded version 2. @ChemRxivchemrxiv.org/doi/full/10.264…
Happy to share our Short Review in Synthesis!
We highlight the unique reactivity of α-ammonio radicals as distonic radical cations and their potential for enabling transformations beyond classical radical chemistry. @thiemechemistrythieme-connect.de/products/e…
Our ChemRxiv preprint has been updated to ver.3: “A Modular Strategy for the Gram-Scale Synthesis of Tetraarylammonium Salts” chemrxiv.org/doi/full/10.264…
Now ready for journal submission!
The first original manuscript from Sato lab is now available in @ChemRxiv
Aromatic fluorination enhances hydrophobicity and antimicrobial activity of magainin 2
chemrxiv.org/doi/full/10.264…
We deeply thank Harada lab at U of Tsukuba and Shigeto lab @kg_chem for their collaboration!
Now online and open access:
Article by Yota Sakakibara, Kei Murakami & co-workers @labmurakami
Taming distonic radical cations for precise γ-C–H functionalization of alkylamines
nature.com/articles/s44160-0…
Congrats, Shumpei, Takumi, and Yota! We report "The Synthesis of Tertiary Alkylamines from Alkyl-Substituted Alkenes Using Amine Umpolung Strategy" in J. Am. Chem. Soc. @J_A_C_Spubs.acs.org/doi/10.1021/jac…
Toguchi, Hamawaki, and Prof. Sakakibara's work is available in @ChemRxiv
A Modular Strategy for the Gram-Scale Synthesis of Tetraarylammonium Salts
chemrxiv.org/doi/full/10.264…
The Synthesis of Tertiary Alkylamines from Alkyl-Substituted Alkenes Using Amine Umpolung Strategy | Journal of the American Chemical Society pubs.acs.org/doi/10.1021/jac…
Thrilled to see the updated version of this work out now on
@ChemRxiv
! It's been a lot of fun exploring the self-assembling properties of this truly unique molecule!
chemrxiv.org/doi/full/10.264…
Our ChemRxiv preprint has been updated to ver.2:
“A Modular Strategy for the Gram-Scale Synthesis of Tetraarylammonium Salts”
chemrxiv.org/doi/full/10.264…
We disclose the physicochemical properties of tetraphenylammonium and achieve the synthesis of chloro-substituted derivatives.
Our ChemRxiv preprint has been updated to ver.2:
“A Modular Strategy for the Gram-Scale Synthesis of Tetraarylammonium Salts”
chemrxiv.org/doi/full/10.264…
We disclose the physicochemical properties of tetraphenylammonium and achieve the synthesis of chloro-substituted derivatives.
We sincerely thank Prof. Sato and Prof. Tanaka (Kwansei Gakuin University), as well as Prof. Maeda and Dr. Horita (Ritsumeikan University), for their insightful discussions and invaluable support.