Spiro cyclohexadienones from the reaction of phenolic enaminone derivatives with hypervalent iodine reagents

被引：7

作者：

Asmanidou, A ^{[1
]}

Papoutsis, I ^{[1
]}

Spyroudis, S ^{[1
]}

Varvoglis, A ^{[1
]}

机构：

[1] Univ Thessaloniki, Dept Chem, Organ Chem Lab, GR-54006 Salonika, Greece

来源：

MOLECULES | 2000年 / 5卷 / 06期

关键词：

spiro cyclohexadienones; hypervalent iodine; enamino esters;

D O I：

10.3390/50600874

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Phenolic enamino compounds, prepared from 2-(4-hydroxyphenyl)-ethylamine and the corresponding beta-keto carbonyl compounds, afford spiro cyclohexadienone derivatives on reaction with hypervalent iodine reagents.

引用

页码：874 / 879

页数：6

共 10 条

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