期刊
ORGANIC LETTERS
卷 11, 期 5, 页码 1047-1049出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol802598c
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资金
- UC Irvine Academic Senate Council on Research, Computing and Library Resources
[Ir(cod)Cl](2) is a highly reactive catalyst for allylation reactions of ketones using allylboronic ester. Mechanistic experiments are consistent with formation of a nucleophilic allylirldium(l) complex that Is activated by the diene ligand toward attack of a ketone. Aryl and alkyl ketones react smoothly at room temperature. Aldimines also undergo allylation under these reaction conditions, requiring increased reaction times relative to the corresponding ketones.
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