Influence of E/Z isomerism of aldoximes on the direction of their alkylation with oxirane

Influence of E/Z isomerism of aldoximes on the direction of their alkylation with oxirane Full article

Journal

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

Output data

Year: 1999, Volume: 48, Number: 7, Pages: 1389-1391 Pages count : 3 DOI: 10.1007/BF02495314

Tags

oxirane; aldoximes; alpha-aryl-N-(2-hydroxyethyl)nitrons

Authors

Bakunova S.M. ¹ , Grigor'ev I.A. ¹ , Volodarsky L.B. ¹

Affiliations

1	Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Acad. Lavrent'eva, 630090, Novosibirsk, Russian Federation

The reaction of Z-2-furaldoxime with oxirane afforded the N-alkylation product, viz., alpha-2-furyl-N-(2-hydroxyethyl)nitron, in good yield. E-Benzaldoxime gave predominantly the O-alkylation product, while its Z isomer was converted into a mixture with the N-alkylation product slightly predominating.

Bakunova S.M. , Grigor'ev I.A. , Volodarsky L.B.
Influence of E/Z isomerism of aldoximes on the direction of their alkylation with oxirane
Russian Chemical Bulletin. 1999. V.48. N7. P.1389-1391. DOI: 10.1007/BF02495314 WOS Scopus РИНЦ OpenAlex

Published print:

Jul 1, 1999

Web of science:	WOS:000082938900038
Scopus:	2-s2.0-0033413179
Elibrary:	13329638
OpenAlex:	W2952137391

DB	Citing
Web of science	5
Scopus	5
Elibrary	4
OpenAlex	2