The preparation of 4,5-dihydro-3-aryl-naphth-[1,2-c]-isoxazoles from dilithiated 1-tetralone oxime and aromatic esters

被引：5
|
作者：
Beam, CF [1 ]
Schady, DA [1 ]
Rose, KL [1 ]
Kelley, W [1 ]
Rakkhit, R [1 ]
Hornsby, CD [1 ]
Studer-Martinez, SL [1 ]
机构：
[1] Coll Charleston, Dept Chem & Biochem, Charleston, SC 29424 USA
来源：
SYNTHETIC COMMUNICATIONS | 2000年 / 30卷 / 18期
基金：
美国国家科学基金会;
关键词：
D O I：
10.1080/00397910008086979
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Dilithiated 1-tetralone oxime was prepared in excess lithium diisopropylamide and condensed with a variety of esters followed by acid cyclization of C-acylated intermediates to substituted 4,5-dihydronaphth-[1,2-c]isoxazoles.
引用
收藏
页码：3391 / 3404
页数：14
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