A short enantioselective synthesis of pipecolic acid
✍ Scribed by Concepción Fernández-García; M.Anthony McKervey
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 125 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Addition of a propargylsilane moiety onto chiral cyclic of an allenic amino acid in the acyclic series; however, this isomerization did not take place with the cyclic α-amino ester iminium ions occurs with a high level of stereoselectivity intermolecularly as well as intramolecularly. This operation
New enantioselective syntheses of N-protected baikiain and pipecolic acid have been developed. The starting material is 2,3-epoxy-5-hexen-1-ol (4) readily available in high ee by Sharpless epoxidation. The regio-and stereoselective epoxide ring-opening by allylamine afforded a doubly unsaturated ami
## 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.