The addition of organolithium reagents to the trianglimine derived from the condensation of enantiopure trans-1,2-diaminocyclohexane and terephthalaldehyde gives the corresponding trianglamine with complete stereoselectivity. The new trianglamine were useful as chiral solvating agents for the determination of the enantiomeric puruty of chiral carboxylic acids by NMR techiques.

D. Savoia, A. Gualandi, H. Stoeckli-Evans, L. Cerisoli (2010). Stereoselective synthesis and applications of ring C-hexasubstituted trianglamines. s.l : Società Chimica Italiana.

Stereoselective synthesis and applications of ring C-hexasubstituted trianglamines

SAVOIA, DIEGO;GUALANDI, ANDREA;CERISOLI, LUCIA
2010

Abstract

The addition of organolithium reagents to the trianglimine derived from the condensation of enantiopure trans-1,2-diaminocyclohexane and terephthalaldehyde gives the corresponding trianglamine with complete stereoselectivity. The new trianglamine were useful as chiral solvating agents for the determination of the enantiomeric puruty of chiral carboxylic acids by NMR techiques.
2010
XXXIII Convegno Nazionale della Divisione di Chimica Organica
P19
P19
D. Savoia, A. Gualandi, H. Stoeckli-Evans, L. Cerisoli (2010). Stereoselective synthesis and applications of ring C-hexasubstituted trianglamines. s.l : Società Chimica Italiana.
D. Savoia; A. Gualandi; H. Stoeckli-Evans; L. Cerisoli
File in questo prodotto:
Eventuali allegati, non sono esposti

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/95178
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact