Isomerization of allylbenzenes

M Hassam, A Taher, GE Arnott, IR Green… - Chemical …, 2015 - ACS Publications
The “phenylpropenoids” are a well-known set of naturally occurring compounds obtained
mainly from plant sources. 1, 2 Of this group, the generalized 2-propenylbenzenes 1 and 1 …

Podophyllotoxin derivatives targeting tubulin: An update (2017–2022)

Y Xu, Z He, L Chen, H Wang - Drug Discovery Today, 2023 - Elsevier
Highlights•We described a detailed account of all the advances on podophyllotoxin
derivatives targeting tubulin from 2017 and 2022.•This review comprehensively summarized …

Synthesis and biological activity, and molecular modelling studies of potent cytotoxic podophyllotoxin-naphthoquinone compounds

HT Nguyen, QGN Thi, THN Thi, PH Thi… - RSC …, 2022 - pubs.rsc.org
A new approach for the synthesis of podophyllotoxin-naphthoquinone compounds using
microwave-assisted three-component reactions is reported in this study. Novel …

Microwave-assisted one-pot synthesis of new phenanthrene fused-tetrahydrodibenzo-acridinones as potential cytotoxic and apoptosis inducing agents

NP Kumar, P Sharma, TS Reddy, N Shankaraiah… - European Journal of …, 2018 - Elsevier
An expeditious microwave-assisted one-pot synthesis of new cytotoxic phenanthrene fused-
tetrahydrodibenzo-acridinones has been successfully accomplished. This protocol offers …

Antineoplastic Agents. 585. Isolation of Bridelia ferruginea Anticancer Podophyllotoxins and Synthesis of 4-Aza-podophyllotoxin Structural Modifications1

GR Pettit, JD Searcy, R Tan, GM Cragg… - Journal of Natural …, 2016 - ACS Publications
Cytotoxic constituents of the terrestrial plant Bridelia ferruginea were isolated using
bioactivity-guided fractionation, which revealed the presence of the previously known …

Multicomponent assembly of 4-aza-podophyllotoxins: A fast entry to highly selective and potent anti-leukemic agents

N Jeedimalla, M Flint, L Smith, A Haces… - European Journal of …, 2015 - Elsevier
The aim of this study was the synthesis and lead structure selection of a best anti-leukemic
agent from a library of aza-podophyllotoxin analogues (APTs). To this end, we report a …

[HTML][HTML] Novel cis-selective and non-epimerisable C3 hydroxy azapodophyllotoxins targeting microtubules in cancer cells

S Kandil, JM Wymant, BM Kariuki, AT Jones… - European Journal of …, 2016 - Elsevier
Podophyllotoxin (PT) and its clinically used analogues are known to be powerful antitumour
agents. These compounds contain a trans fused strained γ-lactone system, a feature that …

Synthesis of Pyrrolo[3,4-b]pyridin-5-ones via Multicomponent Reactions and In Vitro–In Silico Studies Against SiHa, HeLa, and CaSki Human Cervical Carcinoma …

D Segura-Olvera, AN García-González… - Molecules, 2019 - mdpi.com
A series of 12 polysubstituted pyrrolo [3, 4-b] pyridin-5-ones were synthesized via a one-pot
cascade process (Ugi–3CR/aza Diels-Alder/N-acylation/decarboxylation/dehydration) and …

Cu(OAc)2 Catalyzed Synthesis of Novel Chromeno [4,3-b]Pyrano[3,4-e]Pyridine-6,8-Dione Derivatives via a One-Pot Multicomponent Reaction in Water under Mild …

MH Sayahi, Z Afrouzandeh… - Polycyclic Aromatic …, 2022 - Taylor & Francis
An efficient method is introduced based on the copper (II) acetate catalyzed one-pot
multicomponent synthesis of novel chromeno [4, 3-b] pyrano [3, 4-e] pyridine-6, 8-dione …

Intercepted-Knoevenagel condensation for the synthesis of unsymmetrical fused-tricyclic 4H-pyrans

C Shearer, O Desaunay, S Zorc, AD Richaud… - Tetrahedron, 2019 - Elsevier
Abstract 4H-Pyrans (4H-Pys) and 1, 4-dihydropyridines (1, 4-DHPs) are important classes of
heterocyclic scaffolds in medicinal chemistry. Herein, an indium (III)-catalyzed one-pot …