Ruthenium (II)-catalyzed redox-neutral [3+ 2] annulation of indoles with internal alkynes via C–H bond activation: accessing a pyrroloindolone scaffold

Y Xie, X Wu, C Li, J Wang, J Li… - The Journal of Organic …, 2017 - ACS Publications
Ru (II)-catalyzed redox-neutral [3+ 2] annulation reactions of N-ethoxycarbamoyl indoles
and internal alkynes via C–H bond activation are reported. This method features a broad …
被引用次数：48 相关文章

Ruthenium (II)-Catalyzed Redox-Neutral [3+ 2] Annulation of Indoles with Internal Alkynes via C–H Bond Activation: Accessing a Pyrroloindolone Scaffold

Y Xie, X Wu, C Li, J Wang, J Li, H Liu - The Journal of Organic Chemistry, 2017 - Elsevier
ABSTRACT Ru (II)-catalyzed redox-neutral [3+ 2] annulation reactions of N-
ethoxycarbamoyl indoles and internal alkynes via C–H bond activation are reported. This …

Ruthenium (II)-Catalyzed Redox-Neutral [3+ 2] Annulation of Indoles with Internal Alkynes via CH Bond Activation: Accessing a Pyrroloindolone Scaffold

Y Xie, X Wu, C Li, J Wang, J Li… - The Journal of organic …, 2017 - pubmed.ncbi.nlm.nih.gov
Ru (II)-catalyzed redox-neutral [3+ 2] annulation reactions of N-ethoxycarbamoyl indoles
and internal alkynes via CH bond activation are reported. This method features a broad …

Ruthenium (II)-Catalyzed Redox-Neutral [3+ 2] Annulation of Indoles with Internal Alkynes via CH Bond Activation: Accessing a Pyrroloindolone Scaffold.

Y Xie, X Wu, C Li, J Wang, J Li, H Liu - The Journal of Organic …, 2017 - europepmc.org
Ru (II)-catalyzed redox-neutral [3+ 2] annulation reactions of N-ethoxycarbamoyl indoles
and internal alkynes via CH bond activation are reported. This method features a broad …