An efficient conjugate hydrocyanation of chalcones and related enones with TMSCN under solvent-and additive-free microwave conditions
H Iida, T Moromizato, H Hamana, K Matsumoto
Index: Iida, Hirokazu; Moromizato, Tatsuya; Hamana, Hiroshi; Matsumoto, Kiyoshi Tetrahedron Letters, 2007 , vol. 48, # 11 p. 2037 - 2039
Full Text: HTML
Citation Number: 26
Abstract
A first example of solvent-and additive-free 1, 4-addition reaction of α, β-unsaturated ketones such as chalcones, 3-nonen-2-one and benzalacetone with trimethylsilyl cyanide (TMSCN) is described. The addition of TMSCN to chalcones, 3-nonen-2-one, and benzalacetone under microwave irradiation in the absence of Lewis or Brønsted acids and solvents, yielded the corresponding β-cyanoketones in good to moderate yields, as quite rapidly as in 5min. ...
Related Articles:
[Lin, Shaoxia; Wei, Ying; Liang, Fushun Chemical Communications, 2012 , vol. 48, # 79 p. 9879 - 9881]
[Fateen, A.K.; Moustafa, A.H.; Kaddah, A.M.; Shams, N.A. Synthesis, 1980 , # 6 p. 457 - 460]