81683-76-3Relevant articles and documents
REGIOSELECTIVITY OF REACTIONS OF 2-FUROYL-N-ARYL NITRILE IMINE WITH SOME DIPOLAROPHILES
Shawali, Ahmad Sami,Hassaneen, Hamdi Mahmoud,Shetta, Abdel-Fattah,Osman, Abdou,Abdel-Galil, Fathi
, p. 57 - 66 (2007/10/02)
The regioselectivity of the cycloadditions of nitrile imines (1a-d), derived from 2-furoylhydrazidoyl chlorides (3a-d), to the C=C and C=S double bonds of the enol tautomer of acetylacetone and the resonance stabilized thiocyanate anion respectively was investigated.The results indicate that the reactions studied are dipole-LUMO controlled and that the larger orbital coefficient in the LUMO of 7 is on the carbon atom.