Pregled bibliografske jedinice broj: 504559
Sinteza novih N-sulfonilamidina pirimidinske serije
Sinteza novih N-sulfonilamidina pirimidinske serije // Book of abstracts, XXII. Hrvatski skup kemičara i kemijskih inženjera / Pičuljan, Katarina ; Smolec, Sonja (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2011. str. 41-41 (predavanje, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 504559 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Sinteza novih N-sulfonilamidina pirimidinske serije
(Synthesis of novel N-sulfonylamidines in pyrimidine series)
Autori
Krstulović, Luka ; Bajić, Miroslav ; Višnjevac, Aleksandar ; Žinić, Biserka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstracts, XXII. Hrvatski skup kemičara i kemijskih inženjera
/ Pičuljan, Katarina ; Smolec, Sonja - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2011, 41-41
ISBN
978-953-6894-38-3
Skup
XXII. Hrvatski skup kemičara i kemijskih inženjera
Mjesto i datum
Zagreb, Hrvatska, 13.02.2011. - 16.02.2011
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Domaća recenzija
Ključne riječi
N-sulfonilamidini ; pirimidini
(N-sulfonylamidines ; pyrinidines)
Sažetak
Amidines are found in many bioactive natural products [1] and identified as important pharmacophores [2]. Novel N-sulfonylamidines in pyrimidine series were utilized as a part of continous research on potential biologically active compounds. Synthesis involves three component, one-pot, copper catalyzed reaction of terminal alkyne, sulfonyl azide and amine. The reaction is propose to proceed via the formation of ketenimine intermediate, which is generated in situ by the Cu-catalyzed cycloaddition of sulfonyl azide with terminal alkynes followed by the ring opening of resultant triazole copper intermediate which reacts with amine to give three-component coupled product[3]. The structure of all compounds was confirmed on the basis of 1H, 13C NMR spectra and elemental analysis. Analysis by 2D NMR experiments confirmed anti-conformations of the products in DMSO solution and the same conformation was found by X-ray diffraction studies of some compounds. These products are under investigation for their biological activities.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
098-0982914-2935 - Sinteza novih biološki aktivnih derivata nukleobaza i nukleotida (Žinić, Biserka, MZOS ) ( CroRIS)
053-0982914-2965 - Dizajn i sinteza bisamidina sa protutumorskim djelovanjem (Bajić, Miroslav, MZOS ) ( CroRIS)
Ustanove:
Veterinarski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb
Profili:
Aleksandar Višnjevac
(autor)
Miroslav Bajić
(autor)
Biserka Žinić
(autor)
Luka Krstulović
(autor)