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Alkylation of N-substituted-2-phenylacetamides

Alkilovanje n-supstituisanih 2-fenilacetamida

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2004
bitstream_9832.pdf (16.40Mb)
Authors
Mijin, Dušan
Misić-Vuković, Milica
Petrović, Slobodan
Review (Published version)
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Abstract
Various N-substituted phenylacetamides were alkylated using different alkylating agents under neutral and basic conditions. Reactions were performed at different reaction temperatures and in various solvents. Also, a number of various catalysts were used including phase-transfer catalysts. Reactions were followed using GC or GC-MS technique and the presence as well as the yields of the alkylation products were established. Generally, the best yield and high selectivity in the studied reactions were achieved under basic conditions where in the certain cases some products, mostly N-product were obtained solely in quantitative yields.
Različiti N-supstituisani 2-fenilacetamidi su alkilovani koristeći različite agense za alkilovanje u neutralnoj i baznoj sredini. Reakcije su izvođene u različitim rastvaračima i na različitim temperaturama. Korišćeni su i različiti katalizatori, uključujući međufazne katalizatore. Reakcije su praćene upotrebom GC i GC-MS tehnika. Najbolji prinosi kao i selektivnost ostvareni su pri alkilovanju N-supstituisanih 2-fenilacetamida u baznoj sredini pri čemu je N-proizvod nastao u skoro kvantitativnom prinosu.
Keywords:
alkylation / amides / phenylacetamides / alkylation under neutral conditions / alkylation under basic conditions / phase-transfer conditions
Source:
Journal of the Serbian Chemical Society, 2004, 69, 10, 711-736
Publisher:
  • Serbian Chemical Society, Belgrade

ISSN: 0352-5139

WoS: 000224923100001

Scopus: 2-s2.0-31644449084
[ Google Scholar ]
9
7
Handle
https://hdl.handle.net/21.15107/rcub_technorep_606
URI
http://TechnoRep.tmf.bg.ac.rs/handle/123456789/606
Collections
  • Radovi istraživača / Researchers’ publications (TMF)
Institution/Community
Tehnološko-metalurški fakultet
TY  - JOUR
AU  - Mijin, Dušan
AU  - Misić-Vuković, Milica
AU  - Petrović, Slobodan
PY  - 2004
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/606
AB  - Various N-substituted phenylacetamides were alkylated using different alkylating agents under neutral and basic conditions. Reactions were performed at different reaction temperatures and in various solvents. Also, a number of various catalysts were used including phase-transfer catalysts. Reactions were followed using GC or GC-MS technique and the presence as well as the yields of the alkylation products were established. Generally, the best yield and high selectivity in the studied reactions were achieved under basic conditions where in the certain cases some products, mostly N-product were obtained solely in quantitative yields.
AB  - Različiti N-supstituisani 2-fenilacetamidi su alkilovani koristeći različite agense za alkilovanje u neutralnoj i baznoj sredini. Reakcije su izvođene u različitim rastvaračima i na različitim temperaturama. Korišćeni su i različiti katalizatori, uključujući međufazne katalizatore. Reakcije su praćene upotrebom GC i GC-MS tehnika. Najbolji prinosi kao i selektivnost ostvareni su pri alkilovanju N-supstituisanih 2-fenilacetamida u baznoj sredini pri čemu je N-proizvod nastao u skoro kvantitativnom prinosu.
PB  - Serbian Chemical Society, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Alkylation of N-substituted-2-phenylacetamides
T1  - Alkilovanje n-supstituisanih 2-fenilacetamida
EP  - 736
IS  - 10
SP  - 711
VL  - 69
UR  - https://hdl.handle.net/21.15107/rcub_technorep_606
ER  - 
@article{
author = "Mijin, Dušan and Misić-Vuković, Milica and Petrović, Slobodan",
year = "2004",
abstract = "Various N-substituted phenylacetamides were alkylated using different alkylating agents under neutral and basic conditions. Reactions were performed at different reaction temperatures and in various solvents. Also, a number of various catalysts were used including phase-transfer catalysts. Reactions were followed using GC or GC-MS technique and the presence as well as the yields of the alkylation products were established. Generally, the best yield and high selectivity in the studied reactions were achieved under basic conditions where in the certain cases some products, mostly N-product were obtained solely in quantitative yields., Različiti N-supstituisani 2-fenilacetamidi su alkilovani koristeći različite agense za alkilovanje u neutralnoj i baznoj sredini. Reakcije su izvođene u različitim rastvaračima i na različitim temperaturama. Korišćeni su i različiti katalizatori, uključujući međufazne katalizatore. Reakcije su praćene upotrebom GC i GC-MS tehnika. Najbolji prinosi kao i selektivnost ostvareni su pri alkilovanju N-supstituisanih 2-fenilacetamida u baznoj sredini pri čemu je N-proizvod nastao u skoro kvantitativnom prinosu.",
publisher = "Serbian Chemical Society, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Alkylation of N-substituted-2-phenylacetamides, Alkilovanje n-supstituisanih 2-fenilacetamida",
pages = "736-711",
number = "10",
volume = "69",
url = "https://hdl.handle.net/21.15107/rcub_technorep_606"
}
Mijin, D., Misić-Vuković, M.,& Petrović, S.. (2004). Alkylation of N-substituted-2-phenylacetamides. in Journal of the Serbian Chemical Society
Serbian Chemical Society, Belgrade., 69(10), 711-736.
https://hdl.handle.net/21.15107/rcub_technorep_606
Mijin D, Misić-Vuković M, Petrović S. Alkylation of N-substituted-2-phenylacetamides. in Journal of the Serbian Chemical Society. 2004;69(10):711-736.
https://hdl.handle.net/21.15107/rcub_technorep_606 .
Mijin, Dušan, Misić-Vuković, Milica, Petrović, Slobodan, "Alkylation of N-substituted-2-phenylacetamides" in Journal of the Serbian Chemical Society, 69, no. 10 (2004):711-736,
https://hdl.handle.net/21.15107/rcub_technorep_606 .

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