An Olefin Metathesis Based Strategy for the Construction of the JKL, OPQ, and UVW Ring Systems of Maitotoxin
β Scribed by Nicolaou, K. C.; Postema, M. H. D.; Yue, E. W.; Nadin, A.
- Book ID
- 120499117
- Publisher
- American Chemical Society
- Year
- 1996
- Tongue
- English
- Weight
- 179 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A Sequential Electrochemical Oxidation-Olefin Metathesis Strategy for the Construction of Bicyclic Lactam Based Peptidomimetics. -Anodic oxidation of the proline ester (I) and following addition of allylsilane provides 2 allylated prolines of which (III) is elaborated to the dienic compound (V). Its
Armatol F, isolated from the red alga Chondria armata as a polyether triterpene, has a fused tricyclic ether moiety (BCD-ring) with an unusual cis ring junction at C18-C19 between the C-and D-rings. En route to the total synthesis of armatol F, the stereoselective construction of the C18 and C19 ste