抄録
The highly regioselective organocatalytic chlorosilylation of oxirane derivatives using bulky silyl reagents such as (tert-butyl)diphenylsilyl chloride (TBDPSCl) or triphenylsilyl chloride (Ph3SiCl) was developed. The reaction was effectively catalyzed with 4-methoxypyridine N-oxide in the presence of sodium sulfate (Na2SO4). Several silylated halohydrins were obtained with complete regioselectivity and the reaction was applied to the synthesis of carvedilol. (Figure presented.) .
| 本文言語 | English |
|---|---|
| ページ(範囲) | 1886-1891 |
| ページ数 | 6 |
| ジャーナル | Advanced Synthesis and Catalysis |
| 巻 | 358 |
| 号 | 12 |
| DOI | |
| 出版ステータス | Published - 2016 6月 16 |
ASJC Scopus subject areas
- 触媒
- 有機化学
フィンガープリント
「Organocatalytic Regioselective Chlorosilylation of Oxirane Derivatives: Mild and Effective Insertion of Bulky Silyl Chloride by Using 4-Methoxypyridine N-Oxide」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。引用スタイル
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