Rearrangement oftrans-stilbene into diphenylacetaldehyde acetals induced by direct anodic oxidation

Rearrangement oftrans-stilbene into diphenylacetaldehyde acetals induced by direct anodic oxidation Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 1997, Volume: 46, Number: 12, Pages: 2089-2092 Pages count : 4 DOI: 10.1007/bf02495257

Authors

Ogibin Yu.N. ¹ , Ilovaisky A.I. ¹ , Nikishin G.I. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, Moscow, Russian Federation

Direct anodic oxidation oftrans-stilbene in lower alcohols and in some other solvents in the presence of KF or Bu4NBF4 is accompanied by its electrooxidatve rearrangement into diphenylacetaldehyde acetals; a competing reaction yields 1,2-dialkoxy-1,2-diphenylethanes.

Ogibin Y.N. , Ilovaisky A.I. , Nikishin G.I.
Rearrangement oftrans-stilbene into diphenylacetaldehyde acetals induced by direct anodic oxidation
Russian Chemical Bulletin. 1997. V.46. N12. P.2089-2092. DOI: 10.1007/bf02495257 WOS Scopus OpenAlex

Web of science:	WOS:000072504700019
Scopus:	2-s2.0-0031372467
OpenAlex:	W2027342233

DB	Citing
OpenAlex	5
Web of science	4
Scopus	5