Andresini Michael, Colella Marco, Degennaro Leonardo, Luisi Renzo
FLAME-Lab, Flow Chemistry and Microreactor Technology Laboratory Department of Pharmacy-Drug Sciences University of Bari "A. Moro" Via E., Orabona 4-70125 Bari, Italy.
Org Biomol Chem. 2023 Oct 4;21(38):7681-7690. doi: 10.1039/d3ob01382k.
Significant advancements have been made in the synthesis of overlooked aza-S(IV) motifs. The accessibility of sulfinamidines and sulfinimidate esters has greatly improved through the recent development of efficient and complementary synthetic strategies. Intriguingly, new discoveries have emerged regarding the reactivity of these substances, highlighting the electrophilic nature of sulfinimidate esters and the nucleophilic character of sulfinamidines. Moreover, sulfinamidines have been found to be prone to oxidation, leading to the formation of important aza-S(VI) derivatives. In this review, our aim is to present an almost comprehensive overview of the most relevant achievements in the preparation and structural characterization of these overlooked compounds.
在被忽视的氮杂-S(IV) 基序的合成方面已经取得了重大进展。通过高效且互补的合成策略的最新发展,亚磺脒和亚磺亚胺酸酯的可获得性有了极大提高。有趣的是,关于这些物质的反应性出现了新的发现,突出了亚磺亚胺酸酯的亲电性质和亚磺脒的亲核特性。此外,已发现亚磺脒易于氧化,导致形成重要的氮杂-S(VI) 衍生物。在本综述中,我们的目的是对这些被忽视的化合物的制备和结构表征方面最相关的成果进行几乎全面的概述。