The enantioselective total synthesis of (-)-scabronine G is described. The key features of the present synthesis include the construction of a 5-6 ring system containing two quaternary carbon centers via a diastereoselective intramolecular double Michael reaction and the formation of a seven-membered ring using a Prins cyclization.
|Number of pages||4|
|Publication status||Published - 2011 Jun 3|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry