Synthesis of N-substituted 4-hydroxynaphthalimides using palladium-catalysed hydroxylation

被引:18
|
作者
Fleming, Cassandra L. [1 ]
Nalder, Tim D. [1 ,2 ]
Doeven, Egan H. [3 ]
Barrow, Colin J. [1 ]
Pfeffer, Frederick M. [1 ]
Ashton, Trent D. [1 ]
机构
[1] Deakin Univ, Sch Life & Environm Sci, Ctr Chem & Biotechnol, Waurn Ponds, Vic 3216, Australia
[2] New Zealand Inst Plant & Food Res Ltd, Marine Prod Team, 300 Wakefield Quay, Nelson, New Zealand
[3] Deakin Univ, Sch Life & Environm Sci, Ctr Reg & Rural Futures, Waurn Ponds, Vic 3216, Australia
基金
澳大利亚研究理事会;
关键词
Palladium; Hydroxylation; Buchwald-Hartwig; 4-Hydroxy-1,8-naphthalimide; Biarylphosphine; Fluorescence; RATIOMETRIC FLUORESCENT-PROBE; IMAGING HYDROGEN-SULFIDE; ARYL HALIDES; LIVING CELLS; 1,8-NAPHTHALIMIDE DERIVATIVES; PHENOLS; ETHERS;
D O I
10.1016/j.dyepig.2015.11.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Successful implementation of a palladium-mediated hydroxylation of N-substituted 4-chloro-1,8-naphthalimides has been achieved. The methodology detailed herein utilises 4-chloro-1,8-naphthalic anhydride as a starting point and implements the catalyst/ligand combination of Pd(OAc)(2)/t-BuXPhos; all of which are relatively inexpensive. A range of imide substituents tolerated the reaction conditions, including acid sensitive substrates which are not compatible with other existing methodology. As such this approach is not only complimentary to existing procedures, it presents a more direct alternative to accessing 4-hydroxy-1,8-naphthalimides. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:118 / 120
页数:3
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