Improved Synthesis of Cyclic Tertiary Allylic Alcohols by Asymmetric 1,2-Addition of AlMe 3 to Enones
✍ Scribed by Kolb, Andreas; Zuo, Wei; Siewert, Jürgen; Harms, Klaus; von Zezschwitz, Paultheo
- Book ID
- 121810168
- Publisher
- John Wiley and Sons
- Year
- 2013
- Tongue
- English
- Weight
- 338 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0947-6539
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The cinchona alkaloid catalyzed 1,Caddltlon reaction of selenophenols to cyclohexenols has been shown to proceed with asyannetric lnductlon. Optically active selenium adducts are formed in quantitative chemical and up to 43% enanticmeric yields. The transformation to an optically active chiral ally1
## 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.