Pregled bibliografske jedinice broj: 1162114
Construction of tetrasubstituted centers of chirality in isoindolinones via Brønsted acid catalysis
Construction of tetrasubstituted centers of chirality in isoindolinones via Brønsted acid catalysis // 27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts / Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2021. str. 25-25 (pozvano predavanje, nije recenziran, sažetak, znanstveni)
CROSBI ID: 1162114 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Construction of tetrasubstituted centers of
chirality
in isoindolinones via Brønsted acid catalysis
Autori
Gredičak, Matija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts
/ Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna - Zagreb : Hrvatsko kemijsko društvo, 2021, 25-25
Skup
27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI) ; 5. simpozij Vladimir Prelog
Mjesto i datum
Veli Lošinj, Hrvatska, 05.10.2021. - 08.10.2021
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Nije recenziran
Ključne riječi
chirality ; Brønsted acid catalysis
Sažetak
Isoindolinones have attracted much attention among synthetic chemists, as they are integral structural parts of a number of natural products and biologically active compounds. In most cases, only a single enantiomer is effective, or has a better activity profile than the other. Consequently, the synthesis of these structural motifs and the natural products that contain them has been the subject of much elegant and effective research. The most straightforward way to functionalize isoindolinones includes transformations of easily accessible 3- hydroxyisoindolinone precursors. Their ability to form highly reactive species under mild conditions renders them as an attractive substrates in various catalytic reactions. The overview of our recent achievements in the construction of isoindolinone derivatives comprising tetrasubstituted centers of chirality will be presented. The focus will be given on chiral Brønsted acid-catalyzed additions of aromatic and non-aromatic carbon nucleophiles to in situ generated isoindolinone-derived ketimines for the construction of titled compounds. Generally, the transformations proceed smoothly and the corresponding products are isolated predominantly in high yields and enantioselectivities.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2018-01-4053 - Nove strategije za pripravu tetrasupstituiranih kiralnih centara: asimetrične katalitičke reakcije usmjerene protuanionom (NSYNC-ACDC) (Gredičak, Matija, HRZZ - 2018-01) ( CroRIS)
EK-KK.01.1.1.04.0013 - Inovativna rješenja u katalitičkim proizvodnim procesima za potrebe farmaceutske industrije (CAT PHARMA) (Kirin, Srećko, EK ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Matija Gredičak
(autor)