遷移金属含有イリドを鍵活性種とする付加環化反応
スポンサーリンク
概要
- 論文の詳細を見る
The transition metal-catalyzed electrophilic activation of alkynes towards the attack of nucleophiles has been a subject of extensive study due to their high utility as useful methods for the construction of polycyclic compounds.We have found that transition metal-containing carbonyl or azomethine ylides, novel bifunctional metal-containing reactive species, can be generated by treatment of ω-alkynyl carbonyl or imine derivatives with a catalytic amount of electrophilic transition metal complexes such as W(0) and Pt(II) complexes. These species turned out to behave both as an ylide and as a carbene complex during the reaction. Various types of heterocyclic and carbocyclic skeletons could be obtained in a single operation by using these species. Herein, we report the full account of our research based on the above methodology.
- 2012-04-01
著者
関連論文
- 34 タキソールの不斉全合成研究(口頭発表の部)
- レニウム化合物を用いる有機合成反応
- タクスシン・タキソールの不斉全合成
- タキサンジテルペノイド:炭素骨格構築法の開発と不斉全合成 (生物活性天然物の合成--複雑な構造をいかにして構築するか) -- (天然物の合成)
- 78(P04) タキシニンの全合成研究(ポスター発表の部)
- 高原子価・低原子価レニウム
- 遷移金属含有イリドを鍵活性種とする付加環化反応