uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Rational design of asymmetric organocatalysts-increased reactivity and solvent scope with a tetrazolic acid
Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry. Organisk kemi.
Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Chemistry, Department of Chemistry.
2004 (English)In: Tetrahedron Asymmetry, Vol. 15, 1831-1834 p.Article in journal (Refereed) Published
Abstract [en]

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.
Identifiers
URN: urn:nbn:se:uu:diva-69561OAI: oai:DiVA.org:uu-69561DiVA: diva2:97472
Available from: 2005-04-05 Created: 2005-04-05 Last updated: 2011-01-12

Open Access in DiVA

No full text

Authority records BETA

Hartikka, AnttiArvidsson, Per

Search in DiVA

By author/editor
Hartikka, AnttiArvidsson, Per
By organisation
Department of Chemistry

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 275 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf