Department of Organic Chemistry II, University of the Basque Country, P. O. Box 644, 48080 Bilbao, Spain.
Chem Commun (Camb). 2020 Nov 7;56(86):13149-13152. doi: 10.1039/d0cc05981a. Epub 2020 Oct 5.
The enantioselective Michael reaction catalyzed by a bifunctional tertiary amine/squaramide has been used to trigger a Michael/transannular aldol cascade process that leads to densely substituted bicyclo[5.4.0]undecanes and in which three contiguous stereogenic centres, one of them a tertiary alcohol moiety, have been formed in a fully stereocontrolled fashion.
双功能叔胺/酰亚胺催化的对映选择性迈克尔加成反应已被用于引发迈克尔/跨环羟醛缩合级联反应,生成稠合取代的双环[5.4.0]十一烷,其中三个连续的手性中心,包括一个叔醇部分,以完全立体控制的方式形成。