Progress on the Synthesis of the Aromathecin Family of Compounds: An Overview

Author:

Nishiyama Takashi1,Mizuno Shota1,Hieda Yuhzo1,Choshi Tominari1ORCID

Affiliation:

1. Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, 1 Sanzo, Gakuen-cho, Fukuyama 729-0292, Japan

Abstract

We present a systematic review of the methods developed for the synthesis of the aromathecin family of compounds (benz[6,7]indolizino[1,2-b]quinolin-11(13H)-ones) and their derivatives. These methods can be broadly classified into four categories based on the construction of pentacyclic structures: Category 1: by constructing a pyridone moiety (D-ring) on the pyrroloquinoline ring (A/B/C-ring), Category 2: by constructing a pyridine moiety (B-ring) on the pyrroloisoquinolone ring (C/D/E-ring), Category 3: by constructing an indolizidinone moiety (C/D-ring) in a tandem reaction, and Category 4: by constructing a pyrrolidine moiety (C-ring) on the isoquinolone ring (D/E-ring).

Publisher

MDPI AG

Reference39 articles.

1. Plant Antitumor Agents. I. The Isolation and Structure of Camptothecin, a Novel Alkaloidal Leukemia and Tumor Inhibitor from Camptotheca acuminata;Wall;J. Am. Chem. Soc.,1966

2. Indolizidine and quinolizidine alkaloids;Michael;Nat. Prod. Rep.,2005

3. Isolation, total synthesis and biological activity of phenanthroindolizidine and phenanthroquinolizidine alkaloids;Li;Synthesis,2001

4. Camptothecin analogues with enhanced antitumor activity at acidic pH;Adams;Cancer Chemother. Pharmacol.,2000

5. Synthesis of approaches to camptothecin;Shamma;Tetrahedron,1969

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