CLAISEN ORTHOESTER REARRANGEMENT REACTION WITH SECONDARY AND TERTIARY ALLYLIC ALCOHOLS - SYNTHESIS OF 1,2 SECOCHRYSANTHEMATES AND THEIR STRUCTURAL ANALOGS

被引：8

作者：

KELKAR, SV

ARBALE, AA

JOSHI, GS

KULKARNI, GH

机构：

[1] National Chemical Laboratory, Pune

来源：

SYNTHETIC COMMUNICATIONS | 1990年 / 20卷 / 06期

关键词：

D O I：

10.1080/00397919008052329

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A simple route is described for the synthesis of 1,2 Seco-chrysanthemic acid and their structural analogues, employing Claisen orthoester rearrangement reaction in the key-step of synthesis. These acids have been prepared with a view to evaluating some of the esters prepared from them for possible insecticidal and other biological properties. Copyright © 1990 by Taylor & Francis Group. All rights reserved.

引用

页码：839 / 847

页数：9