烯丙基重排
化学
酮
醛
催化作用
酒精氧化
铜
盐(化学)
有机化学
配体(生物化学)
氯化铜
选择性
氯化物
药物化学
生物化学
受体
作者
Ghanashyam Bez,Bala Gangadhar Pasupuleti,Achinta Gogoi
出处
期刊:Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry
[Scientific Publishers of India]
日期:2021-06-29
卷期号:60 (4): 589-597
标识
DOI:10.56042/ijcb.v60i4.39062
摘要
Selective oxidation of benzylic and allylic alcohols to their corresponding aldehyde/ketone derivative without affecting saturated alcohols is still a challenging endeavor in organic synthesis. Various metal complexes, especially the copper complexes in the presence of TEMPO are being used very often for such transformations under aerobic conditions, but they are not selective to allylic and benzylic alcohols. The use of copper salt for oxidation of alcohols in the absence of a ligand are very scarcely studied except for the one catalyzed by CuCl/TEMPO where chloride inhibition and lack of selective oxidation have been noted upon use of CuCl 2 . Herein we report a Cu(OAc) 2 catalyzed and TEMPO mediated selective aerobic oxidation of benzylic and allylic alcohols to aldehyde/ketone in the presence of Et 2 NH. The method avoids pre-synthesis of the catalyst as in the case of Cu(II)/(I) complexes/TEMPO catalyzed oxidation reactions, requires low catalyst loading, employs cheaper copper salt, and gives excellent selectivity for oxidation of benzylic and allylic alcohols.
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