𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reaction of dimethyl acetylenedicarboxylate with 3,4-disubstituted isoxazolin-5-ones. A new synthesis of 1,3-oxazin-6-ones and 2,3-dihydro-1,3-oxazin-6-ones

✍ Scribed by Beccalli, Egle M.; Marchesini, Alessandro; Gelmi, Maria L.; Pilati, Tullio

Book ID
121426338
Publisher
American Chemical Society
Year
1987
Tongue
English
Weight
491 KB
Volume
52
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

The Vilsmeier-Haack reaction with 3,4-di
The Vilsmeier-Haack reaction with 3,4-disubstituted isoxazolin-5-ones. A new synthesis of 1,3-oxazin-6-ones and 1,3-oxazine-2,6-diones.
✍ Egle M. Beccalli; Alessandro Marchesini; Henriette Molinari πŸ“‚ Article πŸ“… 1986 πŸ› Elsevier Science 🌐 French βš– 182 KB

Vilsmeier-Haack type reaction on isoxazolin-5-ones is presented. Recently described is zin-6-ones. 2 The synthetic We report here on the the preparation of a number of E-amino-' and 2-phenyl-6H-1,3-oxapotential of such a class of compounds is well documented.3 syntheses by a Vilsmeier-Haack type rea

A convenient synthesis of 1,3-oxazolidin
A convenient synthesis of 1,3-oxazolidin-4-ones and 1,3-oxazin-4-ones
✍ Klaus Th. Wanner; Ulrich Weber πŸ“‚ Article πŸ“… 1997 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 165 KB

## Abstract 1,3‐Oxazolidin‐4‐ones and 1,3‐oxazin‐4‐ones were synthesized by formal cyclocondensation of imines with α‐ or β‐hydroxy acids.