Levens Alison, Zhang Changhe, Candish Lisa, Forsyth Craig M, Lupton David W
School of Chemistry, Monash University , Clayton 3800, Australia.
Org Lett. 2015 Nov 6;17(21):5332-5. doi: 10.1021/acs.orglett.5b02693. Epub 2015 Oct 20.
An enantioselective N-heterocyclic carbene (NHC)-catalyzed diene regenerative (4 + 2) annulation has been achieved through the use of highly nucleophilic morpholinone-derived catalysts. The reaction proceeds with good to excellent yields, high enantioselectivity (most >92% ee), and good diastereoselectivity (most >7:1). The generality of the reaction is high, with 19 examples reported. The utility of the products has been examined with subsequent derivatization in Diels-Alder reactions using electron-poor dienophiles. Furthermore, interception of the proposed β-lactone intermediate has been achieved, allowing the synthesis of compounds bearing four contiguous stereocenters with high levels of enantio- and diastereoselectivity.
通过使用高亲核性的吗啉酮衍生催化剂,实现了对映选择性N-杂环卡宾(NHC)催化的二烯再生(4 + 2)环化反应。该反应以良好至优异的产率、高对映选择性(大多数>92% ee)和良好的非对映选择性(大多数>7:1)进行。反应的通用性很高,报道了19个实例。通过使用缺电子亲双烯体在狄尔斯-阿尔德反应中进行后续衍生化,对产物的实用性进行了研究。此外,已实现对所提出的β-内酯中间体的捕获,从而能够合成具有高水平对映和非对映选择性的含有四个相邻立体中心的化合物。