Accéder au contenu
Merck

Noncovalent immobilization of ionic-tagged box-Cu(OAc)2 complex and its application in asymmetric Henry reaction.

Chirality (2012-09-25)
Zhi-Huai Li, Zhi-Ming Zhou, Xiao-Yan Hao, Jun Zhang, Xiao Dong, Ying-Qiang Liu
RÉSUMÉ

Immobilized Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding by SBA-15 was applied to asymmetric Henry reaction, and good enantioselectivities were obtained (up to 83% ee) between 2-methoxybenzaldehyde and CH(3)NO(2) in isopropyl alcohol (iPrOH). The catalyst could be reused seven times without any obvious loss in enantioselectivity. For the first time, this facile and clean immobilization method is applied to the use of bis(oxazolines) complexes.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Nitromethane, ACS reagent, ≥95%
Sigma-Aldrich
Benzaldehyde, purified by redistillation, ≥99.5%
Sigma-Aldrich
Nitromethane, ReagentPlus®, ≥99.0%
Sigma-Aldrich
Benzaldehyde, ReagentPlus®, ≥99%
Sigma-Aldrich
2-Methoxybenzaldehyde, 98%
Sigma-Aldrich
Benzaldehyde, ≥98%, FG, FCC
Sigma-Aldrich
Benzaldehyde, natural, FCC, FG
Sigma-Aldrich
Nitromethane, suitable for HPLC, ≥96%
Supelco
Benzaldehyde, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Benzaldehyde, analytical standard
Sigma-Aldrich
Benzaldehyde, puriss. p.a., ≥99.0% (GC)
Benzaldehyde, European Pharmacopoeia (EP) Reference Standard