Emily A. O'Brien, Jeffrey A. Purslow, Brendan J. Wall and Brett VanVeller
Chem. Sci., 2024,15, 18992-18999
Abstract
Amidines are an isostere of the amide bond and are completely unexplored in peptide secondary structure.
Vladimir G. Ilkin, Pavel S. Silaichev, Valery O. Filimonov, Alexey V. Nikulin, Nikolai A. Beliaev, Tetyana V. Beryozkina, Pavel A. Slepukhin, Wim Dehaen and Vasiliy A. Bakulev
New J. Chem., 2026,50, 733-740
Abstract
An azide-free approach toward N-sulfonyl amidines, including phosphorus-containing derivatives based on the reactions of thioamides and thiophosphonyl diamides with iminoiodinanes, was developed.
Samrat Charaimuria and Prodeep Phukan
Green Chem., 2024,26, 11948-11962
Abstract
A magnetically separable nanocatalyst has been developed by the incorporation of CuI on the functionalized surface of cobalt ferrite nanoparticles for the synthesis of N-sulfonyl amidines in aqueous medium at ambient temperature.
Yi Zhang, Renchao Ma, Yongmin Ma and Weiwei Fang
Org. Biomol. Chem., 2025,23, 5111-5115
Abstract
Substrate/reagent-dependent selective annulation of amidines with 2-tert-amino benzaldehydes has been developed.
A. Butrymowicz-Kubiak, A. Topolski, T. M. Muzioł and I. B. Szymańska
Dalton Trans., 2025,54, 9651-9669
Abstract
We report the conventional and mechanochemical ‘green’ synthesis of amidine-carboxylate and imidoylamidinate complexes, their characterization, and evaluation for potential use in gas-assisted methods: CVD, FEBID and FIBID.
![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif)
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