化学
钯
烯丙基重排
二氟
催化作用
酚类
有机化学
药物化学
作者
S. Chen,Luning Tang,Ming Chen
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-10-31
卷期号:26 (45): 9799-9803
被引量:7
标识
DOI:10.1021/acs.orglett.4c03873
摘要
Significant progress has been made in the synthesis of diverse ketals through a palladium-catalyzed reaction involving allylic gem-difluorides and various phenols or alcohols. This methodology facilitates double ipso-defluoroetherification of allylic gem-difluorides, resulting in high product yields with excellent regioselectivity. The reactions were conducted under mild conditions and exhibited outstanding tolerance to a wide range of functional groups. Notably, this approach overcomes the traditional limitation of palladium-catalyzed processes, where nucleophiles typically target the common C-1 position of allylic gem-difluorides, enabling selective functionalization at the rare C-3 position instead.
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