๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Preparation of Acyl Halides under Very Mild Conditions

โœ Scribed by Lee, John B.


Book ID
115469861
Publisher
American Chemical Society
Year
1966
Tongue
English
Weight
272 KB
Volume
88
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Synthesis of acyl halides under very mil
โœ Devos, Alain; Remion, Jeanine; Frisque-Hesbain, Anne-Marie; Colens, Alain; Ghose ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› The Royal Society of Chemistry ๐ŸŒ English โš– 137 KB
Synthesis of acyl halides under very mil
โœ Devos, Alain; Remion, Jeanine; Frisque-Hesbain, Anne-Marie; Colens, Alain; Ghose ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› The Royal Society of Chemistry ๐ŸŒ English โš– 137 KB
Synthesis of tetraphenylporphyrins under
โœ Jonathan S. Lindsey; Henry C. Hsu; Irwin C. Schreiman ๐Ÿ“‚ Article ๐Ÿ“… 1986 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 132 KB

Reaction of pyrrole and an aromatic aldehyde at room temperature affords the corresponding tetraarylporphyrinogen in high yield at thermodynamic equilibrium. Oxidation yields the porphyrin.

Preparation of glycosyl halides under ne
โœ Beat Ernst; Tammo Winkler ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 216 KB

The anomeric hydroxyl group of various furanose andpyranose hemiacetals can be replaced by a fluorine, chlorine, bromine or iodine atom under neutral conditions using haloenamines.