Zobrazeno 1 - 10
of 15
pro vyhledávání: '"JASMINA PREDOJEVIC"'
Publikováno v:
Bulletin of the Chemical Society of Ethiopia, Vol 25, Iss 1, Pp 83-90 (2011)
The synthesis of C7- to C16-alkyl maltosides in the presence of tin(IV) chloride as Lewis acid catalyst was performed. The characterization of the products and theoretical investigation of the crucial step in the synthesis were carried out. The prepa
Externí odkaz:
https://doaj.org/article/7330977ea542479e80e0de1f1f772650
Autor:
VLADIMIR PAVLOVIC, JÁNOS CSANÁDI, SVETISLAV GOJKOVIC, JASMINA PREDOJEVIC, STANIMIR KONSTANTINOVIC
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 8, Pp 499-505 (2001)
The Ferrier rearrangment was used as the key step in the synthesis of C7C16-alkyl 2,3-dideoxy glucosides from glucose and C7C16-alkanols.
Externí odkaz:
https://doaj.org/article/ce67b10291d845de96ae1d4adb2f1a39
Autor:
JÁNOS CSANÁDI, SVETISLAV GOJKOVIC, VLADIMIR PAVLOVIC, STANIMIR KONSTANTINOVIC, JASMINA PREDOJEVIC
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 2, Pp 65-71 (2001)
The SnCl4 catalyzed glycosylation reaction of b-peracetylated sugar derivative (glucose) with fatty alkanols is used in the synthesis of C7 C16 -alkyl glucopyranosides.
Externí odkaz:
https://doaj.org/article/b2c5200899b14425a465e746f93e8424
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 2, Pp 73-80 (2001)
BF3 etherate-induced formation of C3-11 -alkenyl 2,3-unsaturated glucosides was used as the key step in their synthesis from glucose and C3 -C11 -alkenols.
Externí odkaz:
https://doaj.org/article/1560b71480784b9e8bf6c9d0bb9da83a
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 2, Pp 73-80 (2001)
BF3 etherate-induced formation of C3-11-alkenyl 2,3-unsaturated glucosides was used as the key step in their synthesis from glucose and C3-C11-alkenols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d7d1131093f369f0baeb05e3c589b8
http://www.doiserbia.nb.rs/img/doi/0352-5139/2001/0352-51390102073K.pdf
http://www.doiserbia.nb.rs/img/doi/0352-5139/2001/0352-51390102073K.pdf
Autor:
János Csanádi, Stanimir Konstantinovic, Svetislav Gojkovic, Vladimir B. Pavlović, Jasmina Predojevic
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 2, Pp 65-71 (2001)
The SnCl4 catalyzed glycosylation reaction of -peracetylated sugar derivative (glucose) with fatty alkanols is used in the synthesis of C7-C16-alkyl glucopyranosides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::770e8ca0570b630365783a29433d1677
http://www.doiserbia.nb.rs/img/doi/0352-5139/2001/0352-51390102065K.pdf
http://www.doiserbia.nb.rs/img/doi/0352-5139/2001/0352-51390102065K.pdf
Autor:
Stanimir Konstantinovic, Vladimir B. Pavlović, Svetislav Gojkovic, Jasmina Predojevic, János Csanádi
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 8, Pp 499-505 (2001)
The Ferrier rearrangment was used as the key step in the synthesis of C7-C16-alkyl 2,3-dideoxy glucosides from glucose and C7-C16-alkanols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80b380e827968e5f1b74445ee5f7518a
https://doi.org/10.2298/jsc0108499k
https://doi.org/10.2298/jsc0108499k
Publikováno v:
Bulletin of the Chemical Society of Ethiopia. 25
The synthesis of C7- to C16-alkyl maltosides in the presence of tin(IV) chloride as Lewis acid catalyst was performed. The characterization of the products and theoretical investigation of the crucial step in the synthesis were carried out. The prepa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d418d74004730eedff3d8641fddb8464
https://doi.org/10.4314/bcse.v25i1.63368
https://doi.org/10.4314/bcse.v25i1.63368
Publikováno v:
ChemInform. 38
Our investigation elucidates the structure of the intermediate in the first stage of the carboxylation reaction of potassium phenoxide. Under the reduced pressure of carbon dioxide the complex is not solvated with the CO2 molecules. Under the conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4fcdae2d1e25d2d338f348e14553f6f
https://doi.org/10.1002/chin.200740215
https://doi.org/10.1002/chin.200740215
Publikováno v:
Journal of chemical information and modeling. 47(4)
Our investigation elucidates the structure of the intermediate in the first stage of the carboxylation reaction of potassium phenoxide. Under the reduced pressure of carbon dioxide the complex is not solvated with the CO(2) molecules. Under the condi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e61585cc3109e4ac8e566e7c67c30cd
https://pubmed.ncbi.nlm.nih.gov/17511442
https://pubmed.ncbi.nlm.nih.gov/17511442