(S)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
CAS : 78342-42-4
Ref. 3D-FD03725
1g | 237,00 € | ||
2g | 406,00 € | ||
5g | 738,00 € | ||
10g | 1.158,00 € | ||
25g | 1.929,00 € |
Informations sur le produit
- (S)-Schollkopf reagent(S)-2,5-Dimethoxy-3-isopropyl-3,6-dihydropyrazine
- (S)-2-Isopropyl-3,6-dimethoxy-2,5-dihydropyrazine
- (2S)-(+)-2,5-Dihydro-3,6-Dimethoxy-2-Isopropylpyrazine
- (2S)-3,6-dimethoxy-2-(propan-2-yl)-2,5-dihydropyrazine
(S)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine and its enantiomer, (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine, are also known as Schöllkopf chiral auxiliaries or Schöllkopf reagents, and are used to produce optically pure α-amino acids via asymmetric synthesis. The Schöllkopf reagent can be deprotonated at the prochiral α-carbon, and the resulting enolate is trapped with electrophiles to yield adducts with high (typically >95% d.e.) diastereoselectivity. The enolate is essentially planar, and the steric bulk of the isopropyl group directs the incoming electrophile to attack from the opposite face, yielding trans adducts. A wide range of electrophiles including alkyl halides, alkyl sulfonates, acyl chlorides, aldehydes, ketones, epoxides, thioketones and enones can be used. Hydrolysis, typically under mild acidic conditions, yields the non-substituted amino acid with high (typically > 95 e.e.) enantiopurity.
Propriétés chimiques
Question d’ordre technique sur : 3D-FD03725 (S)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine
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