化学
烯烃纤维
烷基
反应条件
组合化学
有机化学
催化作用
作者
David J.-Y.D. Bon,Daniel Chrenko,Ondřej Kováč,Vendula Ferugová,Pavel Lasák,Markéta Fuksová,František Zálešák,Jiří Pospíšil
标识
DOI:10.1002/adsc.202301054
摘要
Abstract In this paper, we present a one‐pot protocol that enables a straightforward and selective transformation of alkyl benzothiazol‐2‐yl and phenyltetrazol‐2‐yl sulfones and acyl chlorides into ketones, E‐olefins, Z‐olefins, and even pyrroles. The final product of the reaction depends on the proper choice of the reaction workup. Notably, the protocol designed for olefin formation allows a switch between E‐ and Z‐olefin formation by the correct choice of the reaction workup. These developed protocols facilitate the formation of all compounds under mild reaction conditions, as evidenced by the synthesis of (nitro)‐fatty acids, and the concept can be extended to other product formations, as demonstrated by the synthesis of pyrroles.
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