[a] See the Supporting Information for details. [b] Ratio of product (P) to starting material (SM) determined by 1H NMR spectroscopy (500 MHz). Number in parentheses is the isolated yield of both diastereomers (on a 0.4 mmol scale). [c] Ratio determined by 1H NMR spectroscopy (500 MHz) prior to purification. [d] Enantiomeric excess of the major diastereomer determined by HPLC. [e] Starting material recovered. [f] Yield of major diastereomer only. … n.d. = not determined.
Corrigendum: Catalytic Dynamic Kinetic Resolutions with N-Heterocyclic Carbenes: Asymmetric Synthesis of Highly Substituted β-Lactones
Article first published online: 3 MAY 2013
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Angewandte Chemie International Edition
Volume 52, Issue 20, page 5203, May 10, 2013
How to Cite
- Issue published online: 3 MAY 2013
- Article first published online: 3 MAY 2013
Vol. 51, Issue 29, 7309–7313, Article first published online: 14 JUN 2012
- asymmetric synthesis;
- dynamic kinetic resolution;
- N-heterocyclic carbenes
Table 1 of this Communication contains wrong data for the ee values of entries 1–7. The corrected entries are shown here.