๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The reaction of thionitrites with barton esters: a convenient free radical chain reaction for decarboxylative nitrosation

โœ Scribed by Pierre Girard; Nadine Guillot; William B. Motherwell; Robyn S. Hay-Motherwell; Pierre Potier


Book ID
104209079
Publisher
Elsevier Science
Year
1999
Tongue
French
Weight
741 KB
Volume
55
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.

โœฆ Synopsis


Tertiary thionitdte esters react with primary and secondary O-acyl derivatives of N-hydroxy-2thiopyridone to give trans nitroso dimers as the principal products of a free radical chain reaction.


๐Ÿ“œ SIMILAR VOLUMES


The reaction of lithium ester enolates w
โœ Michael W. Rathke; Jeffrey Deitch ๐Ÿ“‚ Article ๐Ÿ“… 1971 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 158 KB

Lithium ester enolates, prepared by the reaction of lithium N-isopropylcyclohexylamide (LIICA) with esters at -78' (eq. 1); react with acid chlorides at this same low temperature to provide satisfactory yields of the corresponding S-keto esters (eq. II). This procedure represents an exceedingly vers