A two-directional strategy for the diversity-oriented synthesis of macrocyclic scaffolds

Kieron M. G. O'Connell, Henning S. G. Beckmann, Luca Laraia, Helen T. Horsley, Andreas Bender, Ashok R. Venkitaraman, David R. Spring

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Macrocyclic compounds represent a structural class with exceptional potential for biological activity; however, they have historically been underrepresented in screening collections and synthetic libraries. In this article we report the development of a highly step-efficient strategy for the diversity-oriented synthesis of complex macrocyclic architectures, using a modular approach based on the two-directional synthesis of bifunctional linear precursors and their subsequent combination in a two-directional macrocyclisation process. In this proof of principle study, the synthesis of 14 such compounds was achieved. Cheminformatic analysis of the compounds produced suggests that they reside in biologically relevant regions of chemical space and the compounds were screened for activity against two cancer cell lines.
Original languageEnglish
JournalOrganic and Biomolecular Chemistry
Volume10
Issue number37
Pages (from-to)7545-7551
ISSN1477-0520
DOIs
Publication statusPublished - 2012
Externally publishedYes

Fingerprint Dive into the research topics of 'A two-directional strategy for the diversity-oriented synthesis of macrocyclic scaffolds'. Together they form a unique fingerprint.

Cite this