The Ti-BINOLate-catalyzed, enantioselective ring-opening of meso-aziridines with amines
β Scribed by Peruncheralathan, Saravanan; Aurich, Sandra; Teller, Henrik; Schneider, Christoph
- Book ID
- 120057263
- Publisher
- Royal Society of Chemistry
- Year
- 2013
- Tongue
- English
- Weight
- 444 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1477-0520
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract Catalyzed by the Mg complexes of BINOL derivatives, the enantioselective ring opening reaction of various __meso__βepoxides proceeded smoothly with either aromatic or aliphatic amines as the nucleophiles to afford the corresponding chiral Ξ²βamino alcohols in moderateβtoβhigh yields with