Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Stanimir Konstantinovic"'
Autor:
STANIMIR KONSTANTINOVIC, BILJANA DIMITRIJEVIC, ALEKSANDAR V. TEODOROVIC, SVETISLAV GOJKOVIC, VLADIMIR PAVLOVIC, VESELIN RADULOVIC
Publikováno v:
Journal of the Serbian Chemical Society, Vol 70, Iss 7, Pp 925-929 (2005)
The SnCl4 catalyzed glycosylation reaction of peracetylated b-D-galactopyranose derivatives with terminally unsaturated C3–C11 alkenols was used for the synthesis of some C3–C11 alkenyl b-D-galactopyranosides, as precursors for unsaturated neutra
Externí odkaz:
https://doaj.org/article/a14b1573abd145b99a7bc53a70574617
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
Autor:
Veselin Radulovic, Biljana Dimitrijevic, Svetislav Gojkovic, K Stanimir Konstantinovic, V Aleksandar Teodorovic, D Vladimir Pavlovic
Publikováno v:
Journal of the Serbian Chemical Society, Vol 70, Iss 7, Pp 925-930 (2005)
Journal of the Serbian Chemical Society, Vol 70, Iss 7, Pp 925-929 (2005)
Journal of the Serbian Chemical Society, Vol 70, Iss 7, Pp 925-929 (2005)
The SnCl 4 catalyzed glycosylation reaction of peracetylated p-D-galactopyranose derivatives with terminally unsaturated C 3 -C 1 1 alkenols was used for the synthesis of some C 3 -C 1 1 alkenyl p-D-galactopyranosides, as precursors forunsaturated ne
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.
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.
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.
Publikováno v:
Monatshefte für Chemie / Chemical Monthly. 129:1309-1312
The electrochemical oxidation of diphenyl diselenide in the presence of dienes affords the corresponding cyclic β-phenylselenoethers via an oxyphenylselenation process. The yields of ethers depend on the nature of the diene and on the reaction tempe
Autor:
Rastko D. Vukićević, Stanimir Konstantinovic, Zoran Marković, Mihailo Lj. Mihailović, Ljubinka Joksović
Publikováno v:
Scopus-Elsevier
The acylation of some alicyclic and aliphatic alkenes by the electrochemical generation of a catalyst using a sacrificial aluminum anode was investigated. Substrates were electrolyzed in a dichloromethane solution of an appropriate electrolyte (tetra