Starting from ethyl (S)-lactate as the chiral unit, we have developed the synthesis of the enantiopure bis(3,5)pyrazolophanes 9 and 19 by means of sequential inter- and intramolecular cycloadditions of nitrilimine intermediates. (C) 2000 Elsevier Science Ltd. All rights reserved.

Diastereoselective synthesis of bis(3,5)pyrazolophanes by sequential inter- and intramolecular cycloadditions of homochiral nitrilimines / G. Broggini, G. Molteni, T. Pilati. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 11:9(2000), pp. 1975-1983. [10.1016/S0957-4166(00)00132-4]

Diastereoselective synthesis of bis(3,5)pyrazolophanes by sequential inter- and intramolecular cycloadditions of homochiral nitrilimines

G. Molteni;
2000

Abstract

Starting from ethyl (S)-lactate as the chiral unit, we have developed the synthesis of the enantiopure bis(3,5)pyrazolophanes 9 and 19 by means of sequential inter- and intramolecular cycloadditions of nitrilimine intermediates. (C) 2000 Elsevier Science Ltd. All rights reserved.
Settore CHIM/06 - Chimica Organica
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Caricamento 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/2434/187693
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 22
  • ???jsp.display-item.citation.isi??? 17
social impact