Integrated Research Institute of Pharmaceutical Sciences, College of Pharmacy, The Catholic University of Korea, Bucheon-si 420-743, Korea.
Molecules. 2022 Aug 19;27(16):5304. doi: 10.3390/molecules27165304.
Two novel synthetic approaches for synthesizing ()-3-(1,3-diarylallylidene)oxindoles from oxindole were developed. All previously reported methods for synthesizing 3-(1,3-diarylallylidene)oxindoles utilized palladium-catalyzed reactions as a key step to form this unique skeleton. Despite high efficiency, palladium-catalyzed reactions have limitations in terms of substrate scope. Especially, an iodoaryl moiety cannot be introduced by the previous methods due to its high reactivity toward the palladium catalyst. Our Knoevenagel/allylic oxidation/Wittig and Knoevenagel/aldol/dehydration strategies complement each other and show broad substrate scope, including substrates with iodoaryl groups. The current methods utilized acetophenones, benzylidene phosphonium ylides, and benzaldehydes that are commercially available or easily accessible. Thus, the current synthetic approaches to ()-3-(1,3-diarylallyldiene)oxindoles are readily amendable for variety of oxindole derivatives.
开发了两种从靛红合成()-3-(1,3-二芳基烯丙基)氧化吲哚的新合成方法。以前报道的合成 3-(1,3-二芳基烯丙基)氧化吲哚的所有方法都利用钯催化反应作为形成这种独特骨架的关键步骤。尽管钯催化反应效率很高,但在底物范围方面存在局限性。特别是,由于碘代芳基部分对钯催化剂具有高反应性,以前的方法无法引入。我们的 Knoevenagel/烯丙基氧化/Wittig 和 Knoevenagel/缩合/脱水策略相互补充,具有广泛的底物范围,包括具有碘代芳基部分的底物。当前的方法利用了苯乙酮、亚苄基膦叶立德和苯甲醛,这些都是商业上可获得或容易获得的。因此,()-3-(1,3-二芳基烯丙基)氧化吲哚的当前合成方法易于适用于各种靛红衍生物。