化学
电泳剂
芳基
催化作用
联轴节(管道)
有机化学
醛
对映选择合成
酮
偶联反应
组合化学
烷基
机械工程
工程类
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2025-10-17
摘要
Abstract The preparation of tertiary α-aryl acetals and ketals has been achieved through a Ni-catalyzed reductive cross-coupling approach, utilizing a readily available Ni/Biox catalytic platform. This reaction demonstrates effective enantioselective control over unactivated alkyl radicals adjacent to sterically bulky acetal and ketal groups. The resulting protected tertiary α-aryl ketones and aldehydes are configurationally stable, offering opportunities for further chemical manipulations.
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