Aromatic 1,3-dicarbonyl compounds react with not enolizable aldehydes in the presence of C2H5MgBr or AlCl3 affording 2-carbethoxy- and 2-acetyl-1-indanones via tandem Knoevenagel condensation-cycloalkylation process. © 1995 Elsevier Science Ltd.

Selective synthesis of 1-indanones via tandem knoevenagel condensation-cycloalkylation of β-dicarbonyl compounds and aldehydes / Sartori, G.; Maggi, R.; Bigi, F.; Porta, C.; Tao, X.; Bernardi, G. L.; Ianelli, S.; Nardelli, M.. - In: TETRAHEDRON. - ISSN 0040-4020. - 51:44(1995), pp. 12179-12192. [10.1016/0040-4020(95)00772-Z]

Selective synthesis of 1-indanones via tandem knoevenagel condensation-cycloalkylation of β-dicarbonyl compounds and aldehydes

Sartori G.;Maggi R.;Bigi F.;Porta C.;Ianelli S.;
1995-01-01

Abstract

Aromatic 1,3-dicarbonyl compounds react with not enolizable aldehydes in the presence of C2H5MgBr or AlCl3 affording 2-carbethoxy- and 2-acetyl-1-indanones via tandem Knoevenagel condensation-cycloalkylation process. © 1995 Elsevier Science Ltd.
1995
Selective synthesis of 1-indanones via tandem knoevenagel condensation-cycloalkylation of β-dicarbonyl compounds and aldehydes / Sartori, G.; Maggi, R.; Bigi, F.; Porta, C.; Tao, X.; Bernardi, G. L.; Ianelli, S.; Nardelli, M.. - In: TETRAHEDRON. - ISSN 0040-4020. - 51:44(1995), pp. 12179-12192. [10.1016/0040-4020(95)00772-Z]
File in questo prodotto:
Non ci sono file associati a questo prodotto.

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/11381/2887139
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 21
  • ???jsp.display-item.citation.isi??? ND
social impact