Electrochemically induced synthesis of -lactams, by cyclization (via C3 C4 bond formation) of haloamides XCHR1 CONR2 CHR3 R4 (X: Br, Cl), has been achieved in suitable solvent-supporting electrolyte solutions previously electrolyzed under galvanostatic control. The yields and the stereochemistry of the process are affected by the nature of substituents R1 –R4 and of solvent-supporting electrolyte solutions and by the electrolysis conditions.
An electrochemical alternative strategy to the synthesis of beta-lactams. Part 2 [1] C3-C4 Bond formation / Feroci, Marta; Orsini, M; Rossi, L; Sotgiu, G; Inesi, Achille. - In: ELECTROCHIMICA ACTA. - ISSN 0013-4686. - STAMPA. - 51(2006), pp. 5540-5547. [10.1016/j.electacta.2006.02.026]
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Titolo: | An electrochemical alternative strategy to the synthesis of beta-lactams. Part 2 [1] C3-C4 Bond formation. | |
Autori: | ||
Data di pubblicazione: | 2006 | |
Rivista: | ||
Citazione: | An electrochemical alternative strategy to the synthesis of beta-lactams. Part 2 [1] C3-C4 Bond formation / Feroci, Marta; Orsini, M; Rossi, L; Sotgiu, G; Inesi, Achille. - In: ELECTROCHIMICA ACTA. - ISSN 0013-4686. - STAMPA. - 51(2006), pp. 5540-5547. [10.1016/j.electacta.2006.02.026] | |
Handle: | http://hdl.handle.net/11573/239815 | |
Appartiene alla tipologia: | 01a Articolo in rivista |