Back to Search
Start Over
Facile Synthesis of Tetrahydro-1H-isoindolones via a Sequential Three-Component Copper-Catalyzed Coupling/Propargyl-Allenyl Isomerization/[4 2] Cyclization Reaction.
- Source :
-
Organic Letters . Nov2010, Vol. 12 Issue 21, p5048-5051. 4p. - Publication Year :
- 2010
-
Abstract
- An interesting sequential three-component copper-catalyzed coupling/propargyl-allenyl isomerization/[4 2] cyclization reaction, providing a facile synthesis of highly substituted tetrahydro-1H-isoindolones from conjugated vinylic alkynes, imines, and α,β-unsaturated enoic acid chlorides is reported. The most attractive feature of this transformation is that three stereogenic centers could be generated in one step with high diastereoselectivity. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 15237060
- Volume :
- 12
- Issue :
- 21
- Database :
- Academic Search Index
- Journal :
- Organic Letters
- Publication Type :
- Academic Journal
- Accession number :
- 55150766
- Full Text :
- https://doi.org/10.1021/ol102235t