Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan.
Org Lett. 2020 Dec 18;22(24):9591-9596. doi: 10.1021/acs.orglett.0c03640. Epub 2020 Dec 3.
Herein, we describe the first oxysilylation of unsaturated carboxylic acids mediated by di--butyl peroxide (DTBP), which enables the rapid and efficient preparation of silyl lactone compounds. This process tolerates functional groups, such as methyl, methoxy, halogen (fluoride and chloride), and cyano moieties. Furthermore, the strategy allows the application of a wide range of primary, secondary, and tertiary hydrosilanes for functionalization.
在此,我们描述了由过氧化二叔丁基(DTBP)介导的不饱和羧酸的首次氧化硅烷基化反应,该反应能够快速有效地制备硅烷基内酯化合物。该过程可耐受各种官能团,如甲基、甲氧基、卤素(氟化物和氯化物)和氰基。此外,该策略还允许使用广泛的伯、仲和叔氢硅烷进行官能化。