The synthesis of multifunctional organic catalysts, easily obtained by the condensation of (S)-proline with 1,1'-binaphthyl-2,2'-diamine is reported. These C-2 as well as C, symmetric prolinamides were shown to be able to promote the direct aldol condensation between acetone, methoxyacetone or cyclohexanone and different aldehydes in very good yields and high enantio selectivities.

A multifunctional proline-based organic catalyst for enantioselective aldol reactions / S. Guizzetti, M. Benaglia, L. Pignataro, A. Puglisi. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 17:19(2006), pp. 2754-2760. [10.1016/j.tetasy.2006.10.018]

A multifunctional proline-based organic catalyst for enantioselective aldol reactions

S. Guizzetti
Primo
;
M. Benaglia
;
L. Pignataro
Penultimo
;
A. Puglisi
Ultimo
2006

Abstract

The synthesis of multifunctional organic catalysts, easily obtained by the condensation of (S)-proline with 1,1'-binaphthyl-2,2'-diamine is reported. These C-2 as well as C, symmetric prolinamides were shown to be able to promote the direct aldol condensation between acetone, methoxyacetone or cyclohexanone and different aldehydes in very good yields and high enantio selectivities.
No
English
binam-prolinamides; aldehydes; acid; organocatalysts; design; condensation; derivatives; mannich
Settore CHIM/06 - Chimica Organica
Articolo
Esperti anonimi
Pubblicazione scientifica
2006
Elsevier Science
17
19
2754
2760
7
Pubblicato
Periodico con rilevanza internazionale
ISI:000242765200006
Aderisco
info:eu-repo/semantics/article
A multifunctional proline-based organic catalyst for enantioselective aldol reactions / S. Guizzetti, M. Benaglia, L. Pignataro, A. Puglisi. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 17:19(2006), pp. 2754-2760. [10.1016/j.tetasy.2006.10.018]
reserved
Prodotti della ricerca::01 - Articolo su periodico
4
262
Article (author)
no
S. Guizzetti, M. Benaglia, L. Pignataro, A. Puglisi
File in questo prodotto:
File Dimensione Formato  
TetAs_2006_2754.pdf

accesso riservato

Tipologia: Publisher's version/PDF
Dimensione 165.59 kB
Formato Adobe PDF
165.59 kB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

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/2434/24101
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 74
  • ???jsp.display-item.citation.isi??? 71
social impact