THE SCHMIDT REARRANGEMENT OF METHYL FUROXANYL KETONES AND FUROXANCARBOXYLIC ACIDS - A NEW SYNTHETIC ROUTE TO AMINOFUROXANS

Authors
MAKHOVA NN BLINNIKOV AN KHMELNITSKII LI
Citation
Nn. Makhova et al., THE SCHMIDT REARRANGEMENT OF METHYL FUROXANYL KETONES AND FUROXANCARBOXYLIC ACIDS - A NEW SYNTHETIC ROUTE TO AMINOFUROXANS, Mendeleev communications, (2), 1995, pp. 56-58
Citations number
12
Categorie Soggetti
Chemistry
Journal title
Mendeleev communications → ACNP
ISSN journal
09599436
Issue
2
Year of publication
1995
Pages
56 - 58
Database
ISI
SICI code
0959-9436(1995):2<56:TSROMF>2.0.ZU;2-8
Abstract
The Schmidt rearrangement of methyl furoxanyl ketones and furoxancarbo xylic acids has been carried out for the first time, exemplified by 3, 4-diacetylfuroxan and 4-carboxy-3-(ethoxycarbonyl)furoxan, and this re action has been shown to be a convenient method for the preparation of aminofuroxans.