Kerr, W.J., Lindsay, D., Rankin, E.M., Scott, J.S., and Watson, S.P. (2000) The brucine N-oxide promoted asymmetric Pauson-Khand reaction. Tetrahedron Letters, 41(17), pp. 3229-3233. (doi:10.1016/S0040-4039(00)00357-9)
Full text not currently available from Enlighten.
Publisher's URL: http://dx.doi.org/10.1016/S0040-4039(00)00357-9
The brucine N-oxide-mediated asymmetric Pauson–Khand reaction has been further investigated. It was found that the best levels of enantioselection were obtained with substituted propargylic alcohol complexes. The studies also revealed that when acetone or 1,2-dimethoxyethane is used as the reaction solvent, enhanced levels of enantioselectivity, up to an enantiomeric ratio of 11:89, are achieved.
|Glasgow Author(s) Enlighten ID:||Lindsay, Dr David and Kerr, Professor William|
|Authors:||Kerr, W.J., Lindsay, D., Rankin, E.M., Scott, J.S., and Watson, S.P.|
|College/School:||College of Science and Engineering > School of Chemistry|
|Journal Name:||Tetrahedron Letters|
Enlighten Editors: Update this record