An organocatalytic enantioselective Michael-Michael cascade reaction has been implemented for the creation of structurally variant chiral tetrahydrothiopyrans. The process is realized by employment of new bifunctional ketothioether enones and proceeds highly enantioselectively with formation of four consecutive stereogenic centers.
|Original language||English (US)|
|Number of pages||4|
|State||Published - Feb 7 2014|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry