135064-81-2Relevant articles and documents
Highly stereoselective synthesis of 2-aminobenzylidene derivatives by a convergent 3-component approach
Xu, Zian,Ge, Jingying,Wang, Tianchi,Luo, Ting,Liu, Hongwei,Yu, Xinhong
, p. 2913 - 2917 (2014)
An one-pot stereoselective synthesis of 2-aminobenzylidene derivatives from readily available 5-nitro/cyano-activated 2-halobenzaldehydes (2-chloro-5-nitrobenzaldehyde, 2-bromo-5-nitrobenzaldehyde, 2-fluoro-5-nitrobenzaldehyde, 5-cyano-2-fluorobenzaldehyd
Stereochemical aspects of the "tert-amino effect". Controlled cycloreversion of pyrroloquinoline derivatives and enantioselective introduction of two new optically active centers
Kelderman, E.,Noorlander-Bunt, H. G.,Eerden, J. van,Verboom, W.,Reinhoudt, D. N.
, p. 115 - 123 (2007/10/02)
Conversion of 2-vinyl-N,N-dialkylanilines 2,3(a-o) to pyrroloquinolines 4-13(a-o) occurs via an irreversible suprafacial 1,5 hydrogen shift to a dipolar intermediate which subsequently cyclizes.In refluxing acetonitrile in the presence of zinc chlo