Details

Autor(en) / Beteiligte

• Zhang, Youcan
• Geng, Hui‐Qing
• Wu, Xiao‐Feng

Titel

Palladium‐Catalyzed Perfluoroalkylative Carbonylation of Unactivated Alkenes: Access to β‐Perfluoroalkyl Esters

Ist Teil von

• Angewandte Chemie International Edition, 2021-11, Vol.60 (45), p.24292-24298

Auflage

International ed. in English

Ort / Verlag

Weinheim: Wiley Subscription Services, Inc

Erscheinungsjahr

2021

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Transition‐metal‐catalyzed multi‐component carbonylation represents an efficient strategy for the preparation of various functionalized carbonyl‐containing compounds. Herein, we report a general palladium‐catalyzed perfluoroalkylative carbonylation of unactivated alkenes using inexpensive and readily available carbon monoxide as the C1 source and perfluoroalkyl halides as the coupling partner. A wide range of phenols and alcohols were transformed into the corresponding β‐perfluoroalkyl esters in high yields with broad functional group tolerance and good chemoselectivity. Additionally, alkyl halides can be utilized as alkoxy source as well to give the desired esters. Moreover, several pharmaceutical and bio‐active molecules were also suitable substrates for this one‐pot multi‐component carbonylation process to give the targeted products in good yields. An efficient and convenient palladium‐catalyzed perfluoroalkylative carbonylation of unactivated alkenes has been developed. More than 100 examples of β‐perfluoroalkyl esters were prepared directly from readily available substrates with good functional group tolerance and chemoselectivity.