Original formation of benzyl benzoates by TDAE strategy

被引：11

作者：

Amiri-Attou, Ouassila ^{[1
]}

Terme, Thierry ^{[1
]}

Medebielle, Maurice ^{[2
]}

Vanelle, Patrice ^{[1
]}

机构：

[1] Univ Aix Marseille 2, Fac Pharm, CNRS, Lab Chim Organ Pharmaceut,UMR 6517, F-13385 Marseille 05, France

[2] Univ Lyon 1, CNRS INSA CPE, Lab Synth Electrosynth & React Composes Organ Flu, ICBMS,UMR 5246, F-69622 Villeurbanne, France

来源：

TETRAHEDRON LETTERS | 2008年 / 49卷 / 06期

关键词：

TDAE; aromatic aldehydes; benzyl benzoates; electron transfer;

D O I：

10.1016/j.tetlet.2007.12.011

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We report herein an original photoinduced electron transfer reaction between an aromatic aldehyde and TDAE in the presence of chloromethyl-dimethoxybenzenes. Thus, the reaction of 1-chloromethyl-2,5-dimethoxy-3,4,6-trimethylbenzene (1), dichlorides 4 and 5 with a series of aromatic aldehydes, in the presence of TDAE and under light catalysis, gave the corresponding benzyl benzoates. (c) 2007 Elsevier Ltd. All rights reserved.

引用

收藏

页码：1016 / 1020

页数：5

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