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Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles
- Source :
- Chemical Communications. 56:13429-13432
- Publication Year :
- 2020
- Publisher :
- Royal Society of Chemistry (RSC), 2020.
-
Abstract
- Utilizing the C4 reactive site of cyclopropyl ketones and a chiral N,N'-dioxide-scandium(iii) complex as a catalyst, a concise ring-opening/cyclization/thio-Michael cascade method was developed for the synthesis of chiral benzothiazole derivatives from a simple 2-aminothiophenol material. The kinetic resolution and the origin of stereoselectivity were elucidated via a possible catalytic model.
- Subjects :
- Chemistry
Metals and Alloys
General Chemistry
Combinatorial chemistry
Catalysis
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
Kinetic resolution
chemistry.chemical_compound
Benzothiazole
Cascade reaction
Cascade
Materials Chemistry
Ceramics and Composites
Stereoselectivity
Lewis acids and bases
Reactive site
Subjects
Details
- ISSN :
- 1364548X and 13597345
- Volume :
- 56
- Database :
- OpenAIRE
- Journal :
- Chemical Communications
- Accession number :
- edsair.doi.dedup.....c96dfd99f02ef19804dac725f8ebb877
- Full Text :
- https://doi.org/10.1039/d0cc05667g