抜粋
The double Sonogashira coupling of diiodoparacyclophanes with alkynes proceeded to give planarly chiral dialkynylparacyclophanes; a chiral Pd catalyst, which was prepared in situ from PdCl2(CH 3CN)2 and Taniaphos, realized the first asymmetric Sonogashira coupling with up to ca. 80% ee.
| 元の言語 | English |
|---|---|
| ページ（範囲） | 1870-1872 |
| ページ数 | 3 |
| ジャーナル | Chemical Communications |
| 発行部数 | 14 |
| DOI | |
| 出版物ステータス | Published - 2009 6 25 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry
フィンガープリント The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes' の研究トピックを掘り下げます。これらはともに一意のフィンガープリントを構成します。
これを引用
Kanda, K., Koike, T., Endo, K., & Shibata, T. (2009). The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes. Chemical Communications, (14), 1870-1872. https://doi.org/10.1039/b818904h