REARRANGEMENT OF TRANS-STILBENE INTO DIPHENYLACETALDEHYDE ACETALS INDUCED BY DIRECT ANODIC-OXIDATION

Citation
Yn. Ogibin et al., REARRANGEMENT OF TRANS-STILBENE INTO DIPHENYLACETALDEHYDE ACETALS INDUCED BY DIRECT ANODIC-OXIDATION, Russian chemical bulletin, 46(12), 1997, pp. 2089-2092
Citations number
19
Journal title
ISSN journal
10665285
Volume
46
Issue
12
Year of publication
1997
Pages
2089 - 2092
Database
ISI
SICI code
1066-5285(1997)46:12<2089:ROTIDA>2.0.ZU;2-F
Abstract
Direct anodic oxidation of trans-stilbene in lower alcohols and in som e other solvents in the presence of KF or Bu4NBF4 is accompanied by it s electrooxidatve rearrangement into diphenylacetaldehyde acetals; a c ompeting reaction yields 1,2-dialkoxy-1,2-diphenylethanes.