An Imine Addition/Ring-Closing Metathesis Approach to the Spirocyclic Core of Halichlorine and Pinnaic Acid
Organic Letters2000Vol. 2(13), pp. 1847–1850
Citations Over TimeTop 10% of 2000 papers
Abstract
[reaction: see text] An approach to the spirocyclic core of halichlorine and pinnaic acid has been designed around an imine allylation/ring-closing metathesis sequence. This sequence has been used to generate several azabicylo[n.5] model systems. A newly reported metathesis catalyst was show to be highly effective for cyclization of these systems.
Related Papers
- → Total Synthesis of (+)‐Migrastatin(2006)27 cited
- → Synthesis of N-Substituted Indoles via Aqueous Ring-Closing Metathesis(2020)10 cited
- → 4902764 Polymeric sulfide mineral depressants(1990)2 cited
- → ChemInform Abstract: An Efficient Method for Synthesizing Unsymmetrical Silaketals: Substrates for Ring‐Closing, Including Macrocycle‐Closing, Metathesis.(2008)
- → Nanoparticulate gold oxidation catalyst(2003)