ChemInform Abstract: Expedient Asymmetric Synthesis of (2S,3S)-Boc-phenylalanine Epoxide (X), a Key Intermediate for the Synthesis of Biologically Active Compounds.
β Scribed by Ramon Badorrey; Maria D. Diaz-de-Villegas; Jose A. Galvez
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 37 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Efficient Procedures for the Large-Scale Preparation of (1S,2S)-trans-2-Methoxycyclohexanol, a Key Chiral Intermediate in the Synthesis of Tricyclic Ξ²-Lactam Antibiotics.
Synthetic Studies on Sphingolipids. Part 4. Improved Synthesis of (4S)-4-[(1S,2R)-1,2-Epoxybut-3-enyl]-2-phenyl-2-oxazoline, a Key Intermediate for Sphingolipids. -A novel route to the title compound (VIII) is reported with an oxidative bromination [(VI) β (VII)] as the key step.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
1998 alcohols alcohols (acyclic compounds) P 0110 33 -116 (S)-2-(Dibenzylamino)-3-phenylpropanal as a Chiral Auxiliary: A New Strategy for the Asymmetric Synthesis of 2-Substituted Alcohols. -The key steps in the synthesis of the title alcohols are nucleophilic addition to the aldehyde (I), which p