33047-12-0Relevant articles and documents
A comparison of some pyrolysis reactions of benzotriazoles, benzisoxazolones and benzisothiazolones
Janowski, Wit K.,Prager, Rolf H.,Smith, Jason A.
, p. 3212 - 3216 (2007/10/03)
The products of flash vacuum pyrolysis of N-acetyl, N-methyl, N-benzyl and N-heteroaryl-substituted benzotriazole, 2,1-benzoxazol-3-one and 2,1-benzothiazol-3-one have been compared. The pyrolysis of benzotriazoles and benzisoxazolones appears to involve an iminocarbene intermediate, although the N-benzyl analogues react by radical pathways. Benzisothiazolones appear to form iminoketene intermediates.
Benzisoxazolones: Antimicrobial and antileukemic activity
Wierenga,Evans,Zurenko
, p. 1212 - 1215 (2007/10/02)
An unusual acid-mediated rearrangement of o-nitrostyrene oxide afforded 1-(hydroxymethyl)-2,1-benzisoxazol-3(1H)-one which exhibited broad-spectrum antimicrobial and cytotoxic activity. A number of analogues were prepared by employing a modified zinc-redu
