ЦЕР - Централни Репозиторијум ИХТМ-а
Институт за хемију, технологију и металургију
    • English
    • Српски
    • Српски (Serbia)
  • Српски (ћирилица) 
    • Енглески
    • Српски (ћирилица)
    • Српски (латиница)
  • Пријава
Преглед записа 
  •   ЦЕР
  • IHTM
  • Radovi istraživača / Researchers' publications
  • Преглед записа
  •   ЦЕР
  • IHTM
  • Radovi istraživača / Researchers' publications
  • Преглед записа
JavaScript is disabled for your browser. Some features of this site may not work without it.

Synthesis of vinyldihydropyran by cooperative catalysis

Thumbnail
2016
2048.pdf (387.4Kb)
Аутори
Vulović, Bojan
Maric, Ivana
Matović, Radomir
Saičić, Radomir N.
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документу
Апстракт
Delta(5)-Unsaturated aldehydes with a suitably positioned allylic halide, or phosphate, leaving group undergo doubly-catalyzed cyclization to give dihydropyran derivatives. The cyclization proceeds under the synergetic action of diazabicycloundecene and Pd(PPh3)(4). This type of transformation was also accomplished with an aryl ketone.
Кључне речи:
dihydropyran / cooperative catalysis / cyclization / organopalladium reagents
Извор:
Journal of the Serbian Chemical Society, 2016, 81, 12, 1335-1343
Издавач:
  • Serbian Chemical Soc, Belgrade
Финансирање / пројекти:
  • Развој нових синтетичких метода и њихова примена у синтези природних производа и биолошки активних једињења (RS-172027)

DOI: 10.2298/JSC161102103V

ISSN: 0352-5139

WoS: 000392946100001

Scopus: 2-s2.0-85009739628
[ Google Scholar ]
2
1
URI
https://cer.ihtm.bg.ac.rs/handle/123456789/2050
Колекције
  • Radovi istraživača / Researchers' publications
Институција/група
IHTM
TY  - JOUR
AU  - Vulović, Bojan
AU  - Maric, Ivana
AU  - Matović, Radomir
AU  - Saičić, Radomir N.
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2050
AB  - Delta(5)-Unsaturated aldehydes with a suitably positioned allylic halide, or phosphate, leaving group undergo doubly-catalyzed cyclization to give dihydropyran derivatives. The cyclization proceeds under the synergetic action of diazabicycloundecene and Pd(PPh3)(4). This type of transformation was also accomplished with an aryl ketone.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis of vinyldihydropyran by cooperative catalysis
VL  - 81
IS  - 12
SP  - 1335
EP  - 1343
DO  - 10.2298/JSC161102103V
ER  - 
@article{
author = "Vulović, Bojan and Maric, Ivana and Matović, Radomir and Saičić, Radomir N.",
year = "2016",
abstract = "Delta(5)-Unsaturated aldehydes with a suitably positioned allylic halide, or phosphate, leaving group undergo doubly-catalyzed cyclization to give dihydropyran derivatives. The cyclization proceeds under the synergetic action of diazabicycloundecene and Pd(PPh3)(4). This type of transformation was also accomplished with an aryl ketone.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis of vinyldihydropyran by cooperative catalysis",
volume = "81",
number = "12",
pages = "1335-1343",
doi = "10.2298/JSC161102103V"
}
Vulović, B., Maric, I., Matović, R.,& Saičić, R. N.. (2016). Synthesis of vinyldihydropyran by cooperative catalysis. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 81(12), 1335-1343.
https://doi.org/10.2298/JSC161102103V
Vulović B, Maric I, Matović R, Saičić RN. Synthesis of vinyldihydropyran by cooperative catalysis. in Journal of the Serbian Chemical Society. 2016;81(12):1335-1343.
doi:10.2298/JSC161102103V .
Vulović, Bojan, Maric, Ivana, Matović, Radomir, Saičić, Radomir N., "Synthesis of vinyldihydropyran by cooperative catalysis" in Journal of the Serbian Chemical Society, 81, no. 12 (2016):1335-1343,
https://doi.org/10.2298/JSC161102103V . .

DSpace software copyright © 2002-2015  DuraSpace
О Централном репозиторијуму (ЦеР) | Пошаљите запажања

re3dataOpenAIRERCUB
 

 

Комплетан репозиторијумИнституције/групеАуториНасловиТемеОва институцијаАуториНасловиТеме

Статистика

Преглед статистика

DSpace software copyright © 2002-2015  DuraSpace
О Централном репозиторијуму (ЦеР) | Пошаљите запажања

re3dataOpenAIRERCUB