Syntheses of α- and β-C-Glucopyranosyl Serines from a Common Intermediate
✍ Scribed by Nolen, Ernest G.; Donahue, Laurence A.; Greaves, Rebecca; Daly, Trevor A.; Calabrese, David R.
- Book ID
- 126903198
- Publisher
- American Chemical Society
- Year
- 2008
- Tongue
- English
- Weight
- 120 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1523-7060
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract A flexible common approach for the asymmetric syntheses of sphingofungins E and F is reported, with efficient use of both diastereomers of the Baylis–Hillman adduct in a stereoconvergent manner. Pronounced steric effects of the 2‐substituents in diastereoselective dihydroxylations of (_
The efficient preparation of a-fluoro-~,y-alkenylphosphonate 3, via catalytic hydrogenation of (a-fluoropropargyl)phosphonate ester I, is described. Conjugated fluoroenynes 4 have been synthesized using a modified Homer Wadsworth Emmons (HWE) olefmstion of aldehydes or ketones and I in relatively go
## Abstract Towards total synthesis of a series of kinamycin and related antibiotics __via__ common synthetic intermediates, total synthesis of prekinamycin was achieved __via Suzuki__ coupling of naphthaleneboronic acid and bromobenzene derivative, intramolecular __FriedelCrafts__ reaction of 2‐(