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Catalytic Asymmetric Synthesis of [2,3]-Fused Indoline Heterocycles through Inverse-Electron-Demand Aza-Diels-Alder Reaction of Indoles with Azoalkenes
- Source :
- Angewandte Chemie International Edition. 53:4680-4684
- Publication Year :
- 2014
- Publisher :
- Wiley, 2014.
-
Abstract
- An unprecedented catalytic asymmetric inverse-electron-demand aza-Diels–Alder reaction of indoles with in situ formed azoalkenes is reported. A diverse set of [2,3]-fused indoline heterocycles were achieved in generally good yields (up to 97 %) with high regioselectivity and diastereoselectivity (>20:1 d.r.), and with excellent enantioselectivity (up to 99 % ee).
- Subjects :
- Indole test
Aza Compounds
Indoles
Cycloaddition Reaction
Molecular Structure
Enantioselective synthesis
Regioselectivity
Electrons
Stereoisomerism
General Medicine
General Chemistry
Alkenes
Medicinal chemistry
Catalysis
Cycloaddition
chemistry.chemical_compound
chemistry
Heterocyclic Compounds
Indoline
Organic chemistry
Aza-Diels–Alder reaction
Subjects
Details
- ISSN :
- 14337851
- Volume :
- 53
- Database :
- OpenAIRE
- Journal :
- Angewandte Chemie International Edition
- Accession number :
- edsair.doi.dedup.....4ea5c83cbe2862c7113dd3d0fea32be6
- Full Text :
- https://doi.org/10.1002/anie.201400109