Publications

Zinc metal-promoted nucleophilic addition of azetidin-2-ones to aldehydes and nitriles  (2005)

Authors:
F., Benfatti; G., Cardillo; S., Fabbroni; L., Gentilucci; R., Perciaccante; Piccinelli, Fabio; A., Tolomelli
Title:
Zinc metal-promoted nucleophilic addition of azetidin-2-ones to aldehydes and nitriles
Year:
2005
Type of item:
Articolo in Rivista
Tipologia ANVUR:
Articolo su rivista
Language:
Inglese
Format:
A Stampa
Referee:
Name of journal:
Synthesis
ISSN of journal:
0039-7881
N° Volume:
1
Page numbers:
61-70
Keyword:
zinc; aldehydes; condensation
Short description of contents:
The reactivity of in situ generated organozinc reagents of 3-alkenyl-3-bromoazetidin-2-ones with aromatic and aliphatic aldehydes to give the corresponding alcohol derivatives has been studied. The effect of solvent and Lewis acids has been explored in order to improve the reaction yields. The application of this methodology to nitriles and acyl chlorides allowed the preparation of the corresponding keto derivatives. The products of these reactions could be of interest on account of their structural similarity with the already known cholesterol adsorption inhibitors
Product ID:
81630
Handle IRIS:
11562/736565
Deposited On:
June 6, 2014
Last Modified:
November 26, 2022
Bibliographic citation:
F., Benfatti; G., Cardillo; S., Fabbroni; L., Gentilucci; R., Perciaccante; Piccinelli, Fabio; A., Tolomelli, Zinc metal-promoted nucleophilic addition of azetidin-2-ones to aldehydes and nitriles «Synthesis» , vol. 12005pp. 61-70

Consulta la scheda completa presente nel repository istituzionale della Ricerca di Ateneo IRIS

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