Probing the reactivity of o-phthalaldehydic acid/methyl ester: synthesis of N-isoindolinones and 3-arylaminophthalides

被引:33
作者
Mamidyala, Sreeman K. [1 ]
Cooper, Matthew A. [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, St Lucia, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
EFFICIENT SYNTHESIS; PRIMARY AMINES; ISOINDOLIN-1-ONES; ACID; ANALOGS;
D O I
10.1039/c3cc43838d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new method for the synthesis of N-substituted isoindolinones and 3-arylaminophthalides was developed through aza-Wittig/cyclisation. The reaction of o-phthalaldehydic acid methyl ester with benzylic, aromatic and aliphatic azides gave N-isoindolinones whereas reaction of o-phthalaldehydic acid with the aromatic azides gave 3-arylaminophthalides.
引用
收藏
页码:8407 / 8409
页数:3
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