๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A new and facile synthesis of 3(2H)-furanones via carboxylation- decarboxylation sequence

โœ Scribed by Yoshio Inoue; Kunihiro Ohuchi; Shin Imaizumi

Publisher
Elsevier Science
Year
1988
Tongue
French
Weight
114 KB
Volume
29
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis

One-pot synthesis of 3(2H)-furanones from cl-ethynyl tertiary alcohols and acyl halides has been achieved in the presence of a palladium complex under CO2 pressure.

๐Ÿ“œ SIMILAR VOLUMES

Reduction of ฮ”2-isoxazolines-2. A facile
Reduction of ฮ”2-isoxazolines-2. A facile synthesis of 3(2H)-furanones.
โœ Dennis P. Curran; David H. Singleton ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 200 KB

A simple synthesis of the 3(2H)-furanone ring system is described. The 3(2H)-furanone moeity is a central structural unit in a growing number of natural products including simple compounds such as bullatenone and geiparvarin and more complex compounds such as jatrophone, the eremantholides, and lyc

A facile synthesis of 3-methyl-2H-1-benz
A facile synthesis of 3-methyl-2H-1-benzopyrans via claisen rearrangement
โœ D Gopal; K Rajagopalan ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 117 KB

Several aryl-1(3-bromo-2-methyl-prop-2-ene) ethers 2 have been prep,ared an'd their thermal rearrangements in PEG-405 in the presence of N,N-diethylaniline were Found to yield the title compounds.