Acyclic stereoselection. 43. Stereoselective synthesis of the C-8 to C-15 moiety of erythronolide A
- 1 September 1988
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (20) , 4730-4735
- https://doi.org/10.1021/jo00255a013
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- Acyclic stereoselection. Part 42. 1,4- and 1,5-Stereoselection by sequential aldol addition to a .alpha.,.beta.-unsaturated aldehydes followed by Claisen rearrangement. Application to total synthesis of the vitamin E side chain and the archaebacterial C40 diolThe Journal of Organic Chemistry, 1988
- Diastereo- and enantioselective preparation of β-alkylhomoallylic alcoholsTetrahedron, 1986