Perez Alma R, Hanks Garret T, Bornowski Evan C, Wolfe John P
Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, Michigan 48109-1055, United States.
Org Lett. 2024 May 24;26(20):4361-4364. doi: 10.1021/acs.orglett.4c01400. Epub 2024 May 15.
The palladium-catalyzed cross-coupling of 2-allylphenyl triflate and related electrophiles with substituted indenes affords biindene derivatives in moderate to good yields with high selectivity for thermodynamically preferred alkene isomers. The transformations involve alkene nucleopalladation with indenyl anions, and we also demonstrate that 2-allylphenyl triflates can be transformed to indenes under similar conditions. The scope of this transformation, along with the mechanism of formation of both indene and biindene products, is described.
钯催化的2-烯丙基苯基三氟甲磺酸酯及相关亲电试剂与取代茚的交叉偶联反应,能以中等至良好的产率得到联茚衍生物,且对热力学上更稳定的烯烃异构体具有高选择性。该转化过程涉及茚基阴离子对烯烃的亲核钯化反应,我们还证明了2-烯丙基苯基三氟甲磺酸酯在类似条件下可转化为茚。本文描述了该转化反应的适用范围,以及茚和联茚产物的形成机理。