A novel approach to the pyridoacridine ring system: synthesis of the topoisomerase inhibitor 13-deazaascididemin.

Abstract:

:A novel approach to the pyridoacridine ring system of the ascididemin-type marine alkaloids is presented. This approach allows for the introduction of the ring A of the alkaloids by using a simple aromatic aldehyde building block. The viability of this approach is demonstrated with the synthesis of AK37, a bioactive deaza analogue of the alkaloid ascididemin. Starting from 3-cyano-4-methylquinoline, a sequence of regioselective homolytic benzoylation, annulation of a bromopyridine ring, and radical cyclization leads to the pentacyclic ring system.

journal_name

Arch Pharm (Weinheim)

journal_title

Archiv der Pharmazie

authors

Raeder S,Bracher F

doi

10.1002/ardp.201200019

subject

Has Abstract

pub_date

2012-10-01 00:00:00

pages

822-6

issue

10

eissn

0365-6233

issn

1521-4184

journal_volume

345

pub_type

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