Department of Chemistry, Dalhousie University, 6274 Coburg Road, P.O. 15000, Halifax, Nova Scotia B3H 4R2, Canada.
Org Lett. 2022 Dec 16;24(49):8986-8989. doi: 10.1021/acs.orglett.2c03587. Epub 2022 Dec 1.
Notwithstanding recent developments in nickel-catalyzed C-O cross-coupling chemistry, such transformations of substituted phenols and (hetero)aryl chlorides with a useful reaction scope have yet to be reported. In this work, we disclose the results of catalyst screening that allowed the identification of PhPAd-DalPhos/NiCOD as an effective catalyst system under thermal conditions for the O-arylation of substituted phenols with chloropyridine-type electrophiles, leading to pyridyl--aryl frameworks that are found in active pharmaceutical ingredients.
尽管镍催化的 C-O 交叉偶联化学在最近取得了进展,但具有有用反应范围的取代苯酚和(杂)芳基氯化物的此类转化尚未见报道。在这项工作中,我们披露了催化剂筛选的结果,该筛选允许鉴定 PhPAd-DalPhos/NiCOD 作为在热条件下用于取代苯酚与氯代吡啶型亲电试剂的 O-芳基化的有效催化剂体系,得到了在活性药物成分中发现的吡啶基-芳基骨架。