Accessibility navigation


Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions

Cobb, A.J.A., Shaw, D.M., Longbottom, D.A., Gold, J.B. and Ley, S.V. (2005) Organocatalysis with proline derivatives: improved catalysts for the asymmetric Mannich, nitro-Michael and aldol reactions. Organic & Biomolecular Chemistry, 3 (1). pp. 84-96. ISSN 1477-0520

Full text not archived in this repository.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

To link to this item DOI: 10.1039/b414742a

Abstract/Summary

Tetrazole and acylsulfonamide organocatalysts derived from proline have been synthesised and applied to the asymmetric Mannich, nitro-Michael and aldol reactions to give results that are superior to the proline-catalysed counterpart.

Item Type:Article
Refereed:Yes
Divisions:Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy
ID Code:13776
Uncontrolled Keywords:AMINO-ACID-DERIVATIVES, HIGHLY ENANTIOSELECTIVE SYNTHESIS, ALPHA-AMINO, ONE-POT, HIGH-PRESSURE, ALCOHOL DERIVATIVES, AQUEOUS-MEDIA, IONIC LIQUID, KETONES, ALDEHYDES

University Staff: Request a correction | Centaur Editors: Update this record

Page navigation