Controlled potential oxidation of a variety of substituted o-to-luenesulfonamides at a Pt anode in MeCN using a divided cell provides 3-methyl -4,5-dihydro-1,2,4-benzothiadiazepine-1,1-dioxides selectively and in generally good yields. The scope and limitations of this one-step heterocyclization sequence are also discussed.

ELECTROCHEMICAL HETEROCYCLIZATION OF ORTHO-TOLUENESULFONAMIDES TO 3-ALKYL-4,5-DIHYDRO-1,2,4-BENZOTHIADIAZEPINE-1,1-DIOXIDES / G. PALMISANO, B. DANIELI, G. LESMA, G. FIORI. - In: TETRAHEDRON. - ISSN 0040-4020. - 44:5(1988), pp. 1545-1552. [10.1016/S0040-4020(01)85933-0]

ELECTROCHEMICAL HETEROCYCLIZATION OF ORTHO-TOLUENESULFONAMIDES TO 3-ALKYL-4,5-DIHYDRO-1,2,4-BENZOTHIADIAZEPINE-1,1-DIOXIDES

B. Danieli
Secondo
;
G. Lesma
Penultimo
;
G. Fiori
Ultimo
1988

Abstract

Controlled potential oxidation of a variety of substituted o-to-luenesulfonamides at a Pt anode in MeCN using a divided cell provides 3-methyl -4,5-dihydro-1,2,4-benzothiadiazepine-1,1-dioxides selectively and in generally good yields. The scope and limitations of this one-step heterocyclization sequence are also discussed.
Settore CHIM/06 - Chimica Organica
1988
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
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/2434/183730
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 7
social impact