TY - JOUR
AU - Blacker, A. John
AB - A range of enantiomerically pure 4‐substituted 5‐amino‐1,3‐dioxanes has been condensed with 2‐(2‐bromoethyl)benzaldehyde to produce chiral dihydroisoquinolinium salts, which are effective asymmetric catalysts for the epoxidation of simple alkenes, giving ees of up to 71 %. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
TI - New Chiral Iminium Salt Catalysts for Asymmetric Epoxidation
JF - European Journal of Organic Chemistry
DO - 10.1002/ejoc.200500756
DA - 2006-02-01
UR - https://www.deepdyve.com/lp/wiley/new-chiral-iminium-salt-catalysts-for-asymmetric-epoxidation-DTQiZzm4G7
SP - 803
EP - 813
VL - 2006
IS - 3
DP - DeepDyve
ER -