Journal
ORGANIC LETTERS
Volume 16, Issue 18, Pages 4790-4793Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol5022542
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- ERATO from JST
- Grants-in-Aid for Scientific Research [26288014] Funding Source: KAKEN
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A copper-mediated terminal position-selective C(sp(3))-H acetoxylation using a bidentate directing group and AgOAc as an oxidant was achieved. This reaction has high functional group tolerance and is not affected by steric hindrance. The reaction proceeds in excellent yield, even in gram scale, and the directing group can be removed after the reaction. Aromatic C(sp(2))-H acetoxylation also proceeded under similar reaction conditions.
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