Dynamic kinetic resolution of racemic α-halo acids via a chiral imidazolidinone auxiliary
✍ Scribed by Jeff A. O'Meara; Manfred Jung; Tony Durst
- Book ID
- 103404970
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 196 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Hydrogen transfer reduction of a-sulfonylaldehydes using HCOOH-Et 3 N system as hydrogen source and (S,S)-TsDPEN-based Ru(II) as catalyst proceeds with dynamic kinetic resolution, providing optically active b-sulfonyl primary alcohols in moderate-to-good yields and up to 90% ee.
Enantioselective Synthesis of β-Dibenzylamino Alcohols via a Dynamic Kinetic Resolution of α-Halo Acids. -The title compounds (IV), precursors of synthetically important Reetz aldehydes, are prepared by highly diastereoselective amination of α-bromo esters (I). The high yields obtained in this amin