The stereoselective synthesis of tetrasubstituted alkenylboronates was established via the lithiation/nucleophilic addition reaction of 1,1-organodiboronates to carbonyl compounds. The present approach enables the facile and practical synthesis of tetrasubstituted olefins, which are useful synthetic intermediates for further functionalizations.
|Number of pages||4|
|Journal||Journal of Organic Chemistry|
|Publication status||Published - 2010 May 21|
ASJC Scopus subject areas
- Organic Chemistry