Synthesis and photoinitiating properties of N-substituted 2,6-diisopropylanilines

Synthesis and photoinitiating properties of N-substituted 2,6-diisopropylanilines Full article

Journal

Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393

Output data

Year: 2011, Volume: 47, Number: 6, Pages: 855-861 Pages count : 7 DOI: 10.1134/S1070428011060042

Authors

Kolchina E.F. ¹ , Shekleina N.V. ¹ , Shelkovnikov V.V. ¹

Affiliations

1	Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, pr. Akademika Lavrent’eva 9, Novosibirsk, 630090, Russia

Reactions of 2,6-diisopropylaniline and its 4-bromo and 4-thiocyanato derivatives with methyl iodide in dimethylformamide in the presence of potassium carbonate gave exclusively the corresponding N,N-dimethyl-substituted products. Heating of 2,6-diisopropylaniline and 2,6-diisopropyl-4-thiocyanatoaniline with methyl iodide without a solvent afforded only N-methyl derivatives.

Kolchina E.F. , Shekleina N.V. , Shelkovnikov V.V.
Synthesis and photoinitiating properties of N-substituted 2,6-diisopropylanilines
Russian Journal of Organic Chemistry. 2011. V.47. N6. P.855-861. DOI: 10.1134/S1070428011060042 WOS Scopus РИНЦ

Колчина Е.Ф. , Васильева Н.В. , Шелковников В.В.
Синтез и фотоинициирующие свойства n-производных 2,6-диизопропиланилина
Журнал органической химии (RUSS J ORG CHEM+). 2011. Т.47. №6. С.7-8. РИНЦ

Published print:	Jun 1, 2011
Published online:	Jul 8, 2011

Web of science	WOS:000292562900004
Scopus	2-s2.0-80051510912
Elibrary	18058345
OpenAlex	W2072977838