ChemInform Abstract: Claisen Orthoester Rearrangement Reaction with Secondary and Tertiary Allylic Alcohols: Synthesis of 1,2-Secochrysanthemates and Their Structural Analogues

Autor:	G. H. Kulkarni, S. V. Kelkar, A. A. Arbale, G. S. Joshi
Rok vydání:	1990
Předmět:	Allylic rearrangement chemistry.chemical_compound chemistry Biological property Organic chemistry Rearrangement reaction General Medicine Orthoester
Zdroj:	ChemInform. 21
ISSN:	0931-7597
DOI:	10.1002/chin.199041129
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::32024103e8c61057ab19df9ea71a83dd https://doi.org/10.1002/chin.199041129 Zobrazit plný text záznamu Plný text