Diastereoselective Synthesis of (S)- and (R)-α-Phenylserine by a Sulfinimine-Mediated Strecker Reaction.
✍ Scribed by Alberto Avenoza; Jesus H. Busto; Francisco Corzana; Jesus M. Peregrina; David Sucunza; Maria M. Zurbano
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 22 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Ac acetate; Bz benzoate; PG protecting group; Tris 2,4,6-triisopropylphenylsulfonyl; TES triethylsilyl; TBAF tetrabutylammonium fluoride. [9] A detailed analysis of the synthesis of the metathesis precursors will be reported elsewhere. [10] S. D. Edwards, T. Lewis, R. J. K. Taylor, Tetrahedron Let
## Abstract A novel method for the asymmetric synthesis of __α__,__β__‐diamino acids by using the 2,3,4,6‐tetra‐__O__‐pivaloyl‐__β__‐D‐glucopyranosyl group (Piv~4~Glc) as chiral auxiliary was developed (__Table__ and __Scheme__). The reaction was promoted by CuBr⋅Me~2~S as __Lewis__ acid, and high