22180-78-5Relevant articles and documents
A simple protocol for efficient N-chlorination of amides and carbamates
De Luca, Lidia,Giacomelli, Giampaolo,Nieddu, Giammario
, p. 223 - 226 (2007/10/03)
N-Chlorination of various amides, lactams, and carbamates with very cheap trichloroisocyanuric acid proceeds efficiently under very mild conditions. Excellent results were also observed for the N-chlorination of carbamates of free amino acids.
N-ACYLARENESELENINIMIDOYL CHLORIDES
Derkach, N. Ya.,Lyapina, T. V.,Levchenko, E. S.
, p. 31 - 36 (2007/10/02)
N-Acylseleninimidoyl chlorides were obtained by the reaction of diaryl diselenides, arylselenosilanes, or arylselenium chlorides with the dichloroamides of carboxylic acids.The acid chlorides react with styrene by a scheme of 1,4-cycloaddition with the formation of 4-chloro-2,4,6-triaryl-5,6-dihydro-4-selena-1,3-oxazines.