Synthesis of the C-13 Side Chain Precursors of the 9-Dihydrotaxane Analogue ABT-271
β Scribed by Leanna, M. Robert; DeMattei, John A.; Li, Wenke; Nichols, Paul J.; Rasmussen, Michael; Morton, Howard E.
- Book ID
- 127026568
- Publisher
- American Chemical Society
- Year
- 2000
- Tongue
- English
- Weight
- 63 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1523-7060
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Dihydrodihydroxycinnamic acids and their esters react with acetonitrile or benzonitrile in the presence of sulfuric acid to afford the corresponding syn-b-amino-a-hydroxypropionic acid derivatives. High yields and diastereoselectivity of this transformation allows preparation of various phenylisoser
Oxazoline carboxylic acid 6 as the taxol side chain precursor has been efficiently synthesized via the intramolecular iodoamidation ofatlylic trichloroacetimidate derived from trans-olefinic diol l.