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DOI: 10.1055/s-1999-3435
The Lactone Concept: An Efficient Pathway to Axially Chiral Natural Products and Useful Reagents
Publication History
Publication Date:
31 December 1999 (online)
![](https://www.thieme-connect.de/media/synthesis/199904/lookinside/thumbnails/10.1055-s-1999-3435-1.jpg)
A highly efficient concept for the stereoselective synthesis of axially chiral biaryl target molecules is presented: the atroposelective ring cleavage of configurationally unstable lactone-bridged biaryls. The method has almost no restrictions concerning the substitution pattern, works even for substrates with high steric hindrance at the ortho-position(s) of the axis, and allows the optional, atropo-divergent preparation of each atropisomer from the same biaryl lactone precursor and a recycling of the undesired minor product in the sense of a chiral economy. A brpad series of successful application in natural product and ligand syntheses underlines the high value of the method.
axial chirality - biaryl natural products - biaryl ligands and reagents - atropo-divergent synthesis - lactone-bridged biaryls