Back to Search
Start Over
Organocatalytic Asymmetric C–H Vinylation and Arylation of N-Acyl Tetrahydroisoquinolines
- Source :
- Organic Letters. 17:2396-2399
- Publication Year :
- 2015
- Publisher :
- American Chemical Society (ACS), 2015.
-
Abstract
- The first organocatalytic enantioselective oxidative C-H functionalization of N-acyl tetrahydroisoquinolines with vinyl and aryl boronates promoted by a chiral Brønsted acid is described. This metal-free process tolerates a wide range of electronically varied N-acyl tetrahydroisoquinolines and structurally diverse boronates with good to excellent enantioselectivities.
- Subjects :
- Molecular Structure
Chemistry
Aryl
Organic Chemistry
Enantioselective synthesis
Ethylene Chlorohydrin
Stereoisomerism
Trifluoroethanol
Boronic Acids
Biochemistry
Catalysis
chemistry.chemical_compound
Tetrahydroisoquinolines
Organic chemistry
Physical and Theoretical Chemistry
Brønsted–Lowry acid–base theory
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 17
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....c920007a0849d091ecf6fe0825f23885