Počet záznamů: 1

Diastereoselective and one-pot synthesis of trans-isoquinolonic acids via three-component condensation of homophthalic anhydride, aldehydes, and ammonium acetate catalyzed by aspartic acid

SYSNO ASEP	0435612
Druh ASEP	J - Článek v odborném periodiku
Zařazení RIV	J - Článek v odborném periodiku
Poddruh J	Článek ve WOS
Název	Diastereoselective and one-pot synthesis of trans-isoquinolonic acids via three-component condensation of homophthalic anhydride, aldehydes, and ammonium acetate catalyzed by aspartic acid
Tvůrce(i)	Ghorbani-Choghamarani, A. (IR) Hajjami, M. (IR) Norouzi, M. (IR) Abbasityula, Y. (IR) Eigner, Václav (FZU-D)_{RID, ORCID} Dušek, Michal (FZU-D)_{RID, ORCID, SAI}
Zdroj.dok.	Tetrahedron. - : Elsevier - ISSN 0040-4020 Roč. 69, č. 32 (2013), s. 6541-6544
Poč.str.	4 s.
Jazyk dok.	eng - angličtina
Země vyd.	GB - Velká Británie
Klíč. slova	isoquinolonic acid ; diastereoselective ; aldehyde ; homophthalic anhydride ; ammonium acetate
Vědní obor RIV	CC - Organická chemie
Institucionální podpora	FZU-D - RVO:68378271
UT WOS	000321412000001
EID SCOPUS	84879463642
DOI	10.1016/j.tet.2013.06.010
Anotace	Aspartic acid has been developed as a versatile and highly efficient organocatalyst for the three component combination of homophthalic anhydride, aldehydes, and ammonium acetate to afford transisoquinolonic acids. The reactions were carried out in acetonitrile under reflux conditions. Aspartic acid as an efficient organocatalyst exhibits dramatically improved diastereoselectivity compared with previously reported catalysts for this synthetic strategy.
Pracoviště	Fyzikální ústav
Kontakt	Kristina Potocká, potocka@fzu.cz, Tel.: 220 318 579
Rok sběru	2015

Počet záznamů: 1