Conquering peaks and illuminating depths: developing stereocontrolled organic reactions to unlock nature's macrolide treasure trove. Issue 26 (5th March 2021)

• Record Type: Journal Article
• Authors: Lam, Nelson Y. S.; Stockdale, Tegan P.; Anketell, Matthew J.; Paterson, Ian
• Is Part Of: Chemical communications. Volume 57:Issue 26(2021)
• Page Start: 3171
• Page End: 3189
• Publication Date: 2021-03-05
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/d1cc00442e
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : Exemplified by a representative selection of macrolide natural products, this personal perspective reflects on the trials, tribulations and serendipitous discoveries experienced in pursuit of their total synthesis exploiting aldol methodology. Abstract : The structural complexity and biological importance of macrolide natural products has inspired the development of innovative strategies for their chemical synthesis. With their dense stereochemical content, high level of oxygenation and macrocyclic cores, we viewed the efficient total synthesis of these valuable compounds as an aspirational driver towards developing robust methods and strategies for their construction. Starting out from the initial development of our versatile asymmetric aldol methodology, this personal perspective reflects on an adventurous journey, with all its trials, tribulations and serendipitous discoveries, across the total synthesis, in our group, of a representative selection of six macrolide natural products of marine and terrestrial origin – swinholide A, spongistatin 1, spirastrellolide A, leiodermatolide, chivosazole F and actinoallolide A.