Aukland Miles H, Talbot Fabien J T, Fernández-Salas José A, Ball Matthew, Pulis Alexander P, Procter David J
School of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Pharmaceutical Technology and Development, AstraZeneca, Silk Road Business Park, Macclesfield, SK10 2NA, UK.
Angew Chem Int Ed Engl. 2018 Jul 26;57(31):9785-9789. doi: 10.1002/anie.201805396. Epub 2018 Jul 5.
An interrupted Pummerer/nickel-catalysed cross-coupling strategy has been developed and used in the elaboration of styrenes. The operationally simple method can be carried out as a one-pot process, involves the direct formation of stable alkenyl sulfonium salt intermediates, utilises a commercially available sulfoxide, catalyst, and ligand, operates at ambient temperature, accommodates sp-, sp -, and sp -hybridised organozinc coupling partners, and delivers functionalised styrene products in high yields over two steps. An interrupted Pummerer/cyclisation approach has also been used to access carbo- and heterocyclic alkenyl sulfonium salts for cross-coupling.
一种间断的普默勒尔/镍催化交叉偶联策略已被开发出来,并用于苯乙烯的合成。该操作简单的方法可作为一锅法进行,涉及稳定的烯基锍盐中间体的直接形成,使用市售的亚砜、催化剂和配体,在室温下操作,适用于sp-、sp²-和sp³-杂化的有机锌偶联伙伴,并通过两步反应以高产率得到官能化的苯乙烯产物。一种间断的普默勒尔/环化方法也已被用于制备用于交叉偶联的碳环和杂环烯基锍盐。