Bu4NI-catalyzed α-acyloxylation reaction of ethers and ketones with aldehydes and tert-butyl hydroperoxide

被引：24

作者：

Zhu, Feng ^{[1
]}

Wang, Zhong-Xia ^{[1
]}

机构：

[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China

来源：

TETRAHEDRON | 2014年 / 70卷 / 52期

基金：

中国国家自然科学基金;

关键词：

alpha-Acyloxylation; Ethers; Ketones; TBHP oxidation; Iodide catalysis; FREE OXIDATIVE ESTERIFICATION; CARBOXYLIC-ACIDS; MANGANESE(III) ACETATE; CONJUGATE ADDITION; PRINS CYCLIZATIONS; CARBONYL-COMPOUNDS; COUPLING REACTIONS; LEAD-TETRAACETATE; ACETOXY KETONES; DERIVATIVES;

D O I：

10.1016/j.tet.2014.11.002

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of (hetero)aromatic aldehydes or cinnamaldehyde with di-/multi-ethers in the presence of Bu4NI and tert-butyl hydroperoxide generated corresponding alpha-acyloxy ethers. Reactions between (hetero)aromatic aldehydes or cyclohexanecarbaldehyde with arylalkyl ketones under similar conditions resulted in a-acyloxy ketones. Collectively, Bu4NI-catalyzed alpha-acyloxylation reactions exhibit a broad scope of substrates and a high compatibility with functional groups. (C) 2014 Elsevier Ltd. All rights reserved.

引用

页码：9819 / 9827

页数：9

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