Novel use of Selectfluor™ for the synthesis of cis-fused pyrano-and furanotetrahydroquinolines

被引：32

作者：

Yadav, JS ^{[1
]}

Reddy, BVS ^{[1
]}

Sunitha, V ^{[1
]}

Reddy, KS ^{[1
]}

机构：

[1] Indian Inst Chem Technol, Div Organ Chem, Hyderabad 500007, Andhra Pradesh, India

来源：

ADVANCED SYNTHESIS & CATALYSIS | 2003年 / 345卷 / 11期

关键词：

arylimines; Selectfluor (TM); tetrahydroquinolines;

D O I：

10.1002/adsc.200303101

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

摘要：

Aryl imines formed in situ from aryl aldehydes and aromatic amines undergo smooth [4 + 2] cycloaddition reactions with cyclic enol ethers such as 3,4-dihydro-2H-pyran and 2,3-dihydrofuran in the presence of 10 mol % Selectfluor(TM) in acetonitrile at room temperature to afford pyrano- and furanotetrahydroquinoline derivatives in excellent yields with high endo-selectivity.

引用

页码：1203 / 1206

页数：4

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