Rational design of asymmetric organocatalysts-increased reactivity and solvent scope with a tetrazolic acid
2004 (English)In: Tetrahedron Asymmetry, Vol. 15, 1831-1834 p.Article in journal (Refereed) Published
Replacement of the carboxylic acid functionality in the widely used organocatalyst proline with a tetrazolic acid leads to a catalyst with increased reactivity and solvent scope, as demonstrated in the direct catalytic asymmetric aldol reaction.
Place, publisher, year, edition, pages
2004. Vol. 15, 1831-1834 p.
IdentifiersURN: urn:nbn:se:uu:diva-69561OAI: oai:DiVA.org:uu-69561DiVA: diva2:97472