抄録
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.
本文言語 | English |
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ページ(範囲) | 3469-3472 |
ページ数 | 4 |
ジャーナル | Journal of Organic Chemistry |
巻 | 75 |
号 | 10 |
DOI | |
出版ステータス | Published - 2010 5月 21 |
ASJC Scopus subject areas
- 有機化学