TY  - JOUR
AU  - Milosavljević, Milutin M.
AU  - Marinković, Aleksandar
AU  - Đorđević, Siniša
PY  - 2006
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/975
AB  - A series of N- and N,N-dialkyl-S-alkylthiolcarbamates were synthesized by the rearrangement of N- and N,N-dialkyl-O-alkylthioncarbamates in the presence of diethyl sulfate. The synthesis of some compounds without catalyst was also performed. The compounds were identified by IR, 1H NMR and MS spectroscopic methods. The starting thioncabamates were obtained from the corresponding xanthogenacetates and amines and their structures were also confirmed by IR, 1H NMR and MS data. Some of the thiolcarbamates were characterized for the first time in the literature.
AB  - U radu je izvršena sinteza N- i N,N-dialkil-S-alkiltiolkarbamata premeštanjem N- i N,N-dialkil-O-alkiltionkarbamata u prisustvu katalizatora dietilsulfata. Tako-đe je ispitana mogućnost njihove sinteze bez prisustva katalizatora. Identifikacija sintetisanih jedinjenja je izvršena IR, 1H NMR i MS spektroskopskim metodama. Polazni tionkarbamati su sintetisani iz odgovarajućih ksantogena-cetata i amina, čija struktura je, takođe potvrđena navedenim instrumentalnim metodama. Neki od sintetisanih tiolkarbamata do sada nisu okarakterisani u literaturi.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Synthesis of N-and N,N-dialkyl-S-alkylthiolcarbamates by the rearrangement of N-and N,N-dialkyl-O-thioncarbamates
T1  - Sinteza N- i N,N-dialkil-S-alkiltiol-karbamata premeštanjem N- i N,N-dialkil-O-alkiltionkarbamata
EP  - 32
IS  - 1-2
SP  - 27
VL  - 60
DO  - 10.2298/HEMIND0602027M
ER  - 

@article{
author = "Milosavljević, Milutin M. and Marinković, Aleksandar and Đorđević, Siniša",
year = "2006",
abstract = "A series of N- and N,N-dialkyl-S-alkylthiolcarbamates were synthesized by the rearrangement of N- and N,N-dialkyl-O-alkylthioncarbamates in the presence of diethyl sulfate. The synthesis of some compounds without catalyst was also performed. The compounds were identified by IR, 1H NMR and MS spectroscopic methods. The starting thioncabamates were obtained from the corresponding xanthogenacetates and amines and their structures were also confirmed by IR, 1H NMR and MS data. Some of the thiolcarbamates were characterized for the first time in the literature., U radu je izvršena sinteza N- i N,N-dialkil-S-alkiltiolkarbamata premeštanjem N- i N,N-dialkil-O-alkiltionkarbamata u prisustvu katalizatora dietilsulfata. Tako-đe je ispitana mogućnost njihove sinteze bez prisustva katalizatora. Identifikacija sintetisanih jedinjenja je izvršena IR, 1H NMR i MS spektroskopskim metodama. Polazni tionkarbamati su sintetisani iz odgovarajućih ksantogena-cetata i amina, čija struktura je, takođe potvrđena navedenim instrumentalnim metodama. Neki od sintetisanih tiolkarbamata do sada nisu okarakterisani u literaturi.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Synthesis of N-and N,N-dialkyl-S-alkylthiolcarbamates by the rearrangement of N-and N,N-dialkyl-O-thioncarbamates, Sinteza N- i N,N-dialkil-S-alkiltiol-karbamata premeštanjem N- i N,N-dialkil-O-alkiltionkarbamata",
pages = "32-27",
number = "1-2",
volume = "60",
doi = "10.2298/HEMIND0602027M"
}

Milosavljević, M. M., Marinković, A.,& Đorđević, S.. (2006). Synthesis of N-and N,N-dialkyl-S-alkylthiolcarbamates by the rearrangement of N-and N,N-dialkyl-O-thioncarbamates. in Hemijska industrija
Association of Chemical Engineers of Serbia., 60(1-2), 27-32.
https://doi.org/10.2298/HEMIND0602027M

Milosavljević MM, Marinković A, Đorđević S. Synthesis of N-and N,N-dialkyl-S-alkylthiolcarbamates by the rearrangement of N-and N,N-dialkyl-O-thioncarbamates. in Hemijska industrija. 2006;60(1-2):27-32.
doi:10.2298/HEMIND0602027M .

Milosavljević, Milutin M., Marinković, Aleksandar, Đorđević, Siniša, "Synthesis of N-and N,N-dialkyl-S-alkylthiolcarbamates by the rearrangement of N-and N,N-dialkyl-O-thioncarbamates" in Hemijska industrija, 60, no. 1-2 (2006):27-32,
https://doi.org/10.2298/HEMIND0602027M . .