Arylglyoxals in synthesis of heterocyclic compounds

B Eftekhari-Sis, M Zirak, A Akbari - Chemical reviews, 2013 - ACS Publications
Heterocycles are an extraordinarily important class of compounds, making up more than half
of all known organic compounds. Heterocycles are present in a wide variety of drugs, most …

Extending nature's leads: the anticancer agent ellipticine

NC Garbett, DE Graves - Current Medicinal Chemistry-Anti …, 2004 - ingentaconnect.com
The natural plant product ellipticine was isolated in 1959 from the Australian evergreen tree
of the Apocynaceae family. This compound was found to be an extremely promising …

Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1, 2-diamines

S Antoniotti, E Duñach - Tetrahedron Letters, 2002 - Elsevier
Direct and catalytic synthesis of quinoxaline derivatives from epoxides and ene-1,2-diamines -
ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …

Zn [(L) proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room temperature

MM Heravi, MH Tehrani, K Bakhtiari… - Catalysis Communications, 2007 - Elsevier
Zn[(l)proline]: A powerful catalyst for the very fast synthesis of quinoxaline derivatives at room
temperature - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books …

Spectroscopic and thermodynamic studies on the binding of sanguinarine and berberine to triple and double helical DNA and RNA structures

S Das, GS Kumar, A Ray, M Maiti - Journal of Biomolecular …, 2003 - Taylor & Francis
A comparative study on the interaction of sanguinarine and berberine with DNA and RNA
triplexes and their parent duplexes was performed, by using a combination of …

Studies of the reactions between indole-2, 3-diones (isatins) and 2-aminobenzylamine

J Bergman, R Engqvist, C Stålhandske, H Wallberg - Tetrahedron, 2003 - Elsevier
Reflux of equimolecular amounts 2-aminobenzylamine and isatins in acetic acid produced
indolo [3, 2-c] quinolin-6-ones in good yields. A proposed mechanism involving initial …

Novel nano-size and crab-like biological-based glycoluril with sulfonic acid tags as a reusable catalyst: Its application to the synthesis of new mono-and bis …

M Zarei, H Sepehrmansourie, MA Zolfigol… - New Journal of …, 2018 - pubs.rsc.org
Herein novel crab-like biological-based glycoluril with sulfonic acid tags, namely glycoluril
tetrakis (butane-1-sulfonic acid)(GTBSA), was prepared in nano-size form and fully …

An expedient microwave assisted regio-and stereoselective synthesis of spiroquinoxaline pyrrolizine derivatives and their AChE inhibitory activity

AM Akondi, S Mekala, ML Kantam, R Trivedi… - New Journal of …, 2017 - pubs.rsc.org
In this study, we report an efficient four-component cascade protocol to afford spiro indeno
[1, 2-b] quinoxaline-11, 3′-pyrrolizines via the condensation of ninhydrin …

Interactions of Antiviral Indolo[2,3-b]quinoxaline Derivatives with DNA

LM Wilhelmsson, N Kingi… - Journal of medicinal …, 2008 - ACS Publications
Here, we present the synthesis of five novel indoloquinoxaline derivatives and investigate
the DNA binding properties of these monomeric as well as dimeric compounds using …

One-Pot Construction of Indolo[2,3-b]quinoxalines through Ruthenium-Catalyzed Ortho C–H Bond Functionalization of 2-Arylquinoxalines with Sulfonyl Azides

S Laru, S Bhattacharjee, S Ghosh, A Hajra - Organic Letters, 2021 - ACS Publications
The synthesis of N-substituted indolo [2, 3-b] quinoxalines has been developed through a
Ru (II)-catalyzed ortho C–H functionalization of 2-arylquinoxalines with sulfonyl azides and …