25939-33-7Relevant academic research and scientific papers
Preparation of methyl N-substituted carbamates from amides through N-chloroamides
Hiegel, Gene A.,Hogenauer, Tyrone J.
, p. 2091 - 2098 (2005)
Amides are chlorinated on the nitrogen using trichloroisocyanuric acid, and the N-chloroamides are then rearranged to the corresponding methyl N-substituted carbamates by sodium methoxide in methanol. Copyright Taylor & Francis, Inc.
Preparation of N-chloroamides using trichloroisocyanuric acid
Hiegel, Gene A.,Hogenauer, Tyrone J.,Lewis, Justin C.
, p. 2099 - 2105 (2007/10/03)
Amides are efficiently converted to N-chloroamides by trichloroisocyanuric acid in methanol. Copyright Taylor & Francis, Inc.
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.
BEHAVIOUR OF NITRILE OXIDES TOWARDS NUCLEOPHILES. VI. SYNTHESIS AND POLYMERIZATION OF ALIPHATIC NITRILE OXIDES
Sarlo, Francesco De,Guarna, Antonio,Brandi, Alberto,Mascagni, Paolo
, p. 341 - 344 (2007/10/02)
Some new aliphatic nitrile oxides have been prepared and allowed to react with pyridine or trimethylamine in ethanol: as for acetonitrile oxide, they undergo polymerization to cyclic oligomers or higher polymers.Linking of monomer units through C-O bonds
