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

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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 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.

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Item Type Article
URI https://reading-clone.eprints-hosting.org/id/eprint/13776
Identification Number/DOI 10.1039/b414742a
Refereed Yes
Divisions Life Sciences > School of Chemistry, Food and Pharmacy > School of Pharmacy
Uncontrolled Keywords AMINO-ACID-DERIVATIVES, HIGHLY ENANTIOSELECTIVE SYNTHESIS, ALPHA-AMINO, ONE-POT, HIGH-PRESSURE, ALCOHOL DERIVATIVES, AQUEOUS-MEDIA, IONIC LIQUID, KETONES, ALDEHYDES
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