Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • 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
Determination of the relative configuration of vic-amino alcohols
KTH, Superseded Departments, Chemistry.
2003 (English)In: Tetrahedron Letters, ISSN 0040-4039, E-ISSN 1359-8562, Vol. 44, no 6, 1279-1281 p.Article in journal (Refereed) Published
Abstract [en]

A large set of syn- and anti-1,2-amino alcohols has been synthesized. Upon comparison of the CHO and CHN H-1 NMR shifts a general trend has been observed, making it possible to determine the relative configuration of 1,2-amino alcohols without derivatization or shift reagents.

Place, publisher, year, edition, pages
2003. Vol. 44, no 6, 1279-1281 p.
Keyword [en]
amino alcohols, configuration, NMR, circular-dichroism spectra, beta-amino, asymmetric-synthesis, enantiomeric purity, acid, access, nmr
Identifiers
URN: urn:nbn:se:kth:diva-22223ISI: 000180731300039OAI: oai:DiVA.org:kth-22223DiVA: diva2:340921
Note
QC 20100525Available from: 2010-08-10 Created: 2010-08-10 Last updated: 2017-12-12Bibliographically approved

Open Access in DiVA

No full text

Search in DiVA

By author/editor
Somfai, Peter
By organisation
Chemistry
In the same journal
Tetrahedron Letters

Search outside of DiVA

GoogleGoogle Scholar

urn-nbn

Altmetric score

urn-nbn
Total: 25 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • 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