Abstract
The structures of natural products from a variety of sources contain spirocycles, two rings that share a common atom. The spiro motif is finding increasing inclusion in drug candidates, and as a structural component in several promising classes of chiral ligands used in asymmetric synthesis. Total syntheses of products containing all-carbon spirocycles feature several common methods of ring closure which we examine in this review.
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CITATION STYLE
Smith, L. K., & Baxendale, I. R. (2015, September 1). Total syntheses of natural products containing spirocarbocycles. Organic and Biomolecular Chemistry. Royal Society of Chemistry. https://doi.org/10.1039/c5ob01524c
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