13584-99-1Relevant academic research and scientific papers
A non-MIC route to carbamates: Irreversible trans-esterification reaction of methyl N-methylcarbamate with phenolic substrates possessing additional functional groups
Kumaran, G.,Naik, R. H.,Kulkarni, G. H.
, p. 893 - 895 (2007/10/02)
The novel non-MIC route to aryl carbamates, involving irreversible trans-esterification of methyl N-methylcarbamate has been carried out on a variety of phenolic substrates possessing additional functional groups for studying the scope of the reaction.The carbamates, thus synthesised, have been screened for their insecticidal activity against Musca domestica.
SYNTHESIS OF A NUMBER OF DERIVATIVES OF ALKALOIDS AND OF NITROGEN-CONTAINING HETEROCYCLES AND THEIR ANTICHOLINESTERASE ACTIVITIES
Dalimov, D. N.,Karimov, D. T.,Vaizburg, G. N.,Abduvakhabov, A. A.,Abdullaeva, L. K.,Kamaev, F. G.
, p. 702 - 708 (2007/10/02)
N-Methyl- and N-phenylcarbamates based on a number of alkaloids and nitrogen-containing heterocycles have been synthesized, and they have proved to be weak irreversible inhibitors of acetylcholinesterase and butyrylcholinesterase.It has been shown that th
