Enantioselective Total Synthesis of the Antihypertensive Agent (S,R,R,R)-Nebivolol
β Scribed by S Chandrasekhar; M Venkat Reddy
- Book ID
- 104202877
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 136 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
AbstractΓThe total synthesis of (S,R,R,R)-Nebivolol, a hypertensive agent, is reported. Claisen rearrangement and a one-pot Sharpless asymmetric epoxidation, intramolecular epoxide opening with internal phenoxide anion to generate the chiral chromane are the key steps.
π SIMILAR VOLUMES
Enantioselective Total Synthesis of the (-)-(6R,11R,14S)-Isomer of Colletallol. -The total synthesis of title compound (VII) is based on two consecutive Wittig reactions, the first one intermolecular and the second one intramolecular, instead of classical macrolactonizations. The strategy is flexibl