A CYCLOADDITION APPROACH TO 3-ACYLTETRAMIC AND 3-ACYLTETRONIC ACIDS

Authors
JONES RCF BHALAY G CARTER PA DULLER KAM VULTO SIE
Citation
Rcf. Jones et al., A CYCLOADDITION APPROACH TO 3-ACYLTETRAMIC AND 3-ACYLTETRONIC ACIDS, Journal of the Chemical Society. Perkin transactions. I, (18), 1994, pp. 2513-2515
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of the Chemical Society. Perkin transactions. I → ACNP
ISSN journal
0300922X
Issue
18
Year of publication
1994
Pages
2513 - 2515
Database
ISI
SICI code
0300-922X(1994):18<2513:ACAT3A>2.0.ZU;2-F
Abstract
1,3-Dipolar cycloaddition of nitrile oxides to enamines formed from pr otected-gamma-amino- or gamma-hydroxy-beta-keto esters affords isoxazo lecarboxylic esters that can be converted into 3-acyltetramic acids vi a dihydropyrroloisoxazol-4-ones, or into 3-acyltetronic acids.