芳基
试剂
烷基
催化作用
化学
偶联反应
催化循环
联轴节(管道)
格氏试剂
有机化学
药物化学
组合化学
材料科学
冶金
作者
Alois Fürstner,Andreas Leitner
标识
DOI:10.1002/1521-3773(20020215)41:4<609::aid-anie609>3.0.co;2-m
摘要
Aryl chlorides are better substrates than the corresponding bromides or iodides in the presented cross-coupling with alkyl Grignard reagents that is catalyzed by iron salts (see scheme); even aryl tosylates are converted efficiently. This situation is attributed to a novel catalytic cycle, which probably involves iron complexes with formally negative oxidation states (probably Fe−II).
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