124525-62-8Relevant articles and documents
Direct Intermolecular C-H Functionalization Triggered by 1,5-Hydride Shift: Access to N-Arylprolinamides via Ugi-Type Reaction
Zhen, Le,Wang, Jiankun,Xu, Qing-Long,Sun, Hongbin,Wen, Xiaoan,Wang, Guangji
supporting information, p. 1566 - 1569 (2017/04/13)
A novel Ugi-type reaction triggered by 1,5-hydride shift has been established, giving access to N-arylprolinamides and related compounds in high atom economy and good yields. This is an example of a two starting material-three component reaction. The benz
Efficient cyclization of tertiary amines and alkenes promoted by KOt-Bu-DMF
Chen, Yan-Yan,Zhang, Xue-Jing,Yuan, Hui-Min,Wei, Wen-Tao,Yan, Ming
supporting information, p. 10974 - 10976 (2013/11/19)
Nitrogen heterocycles could be prepared in good yields via intramolecular cyclization of tertiary amines and alkenes promoted by KOt-Bu-DMF. This journal is The Royal Society of Chemistry 2013.
The "tert-amino effect" in heterocyclic chemistry: synthesis of tetra- and pentacyclic compounds
Nijhuis, W. H. N.,Leus, G. R. B.,Egberink, R. J. M.,Verboom, W.,Reinhoudt, D. N.
, p. 172 - 178 (2007/10/02)
A new and covenient route for the synthesis of several heterotetra- and pentacyclic compounds is presented.Heating the 2-vinyl-N,N-dialkylanilines 3a-h, synthesized from the aldehydes 2a-f,h or the acetophenone 2g and malonitrile or ethyl cyanoacetate, in
