Reaction of 1-Trimethylsilyl-3-chloro-1-propyne with α-Nitroacetophenone
…, NV Gritsai, VD Buikliskii, ED Mel'nikova
Index: Yurchenko; Dybova; Gritsai; Buikliskii; Mel'nikova Russian Journal of Organic Chemistry, 2002 , vol. 38, # 2 p. 292 - 294
Full Text: HTML
Citation Number: 1
Abstract
Unlike b-diketones the a-nitroacetophenone failed to react with compound I under the same conditions. The reaction of 1-trimethylsilyl-3-chloro-1-propyne with a-nitroacetophenone in the presence of equimolar amounts of KI and sodium ethylate afforded only 1-trimethylsilyl-3- iodo-1-propyne (III) that as the compound I did not enter further into C-alkylation reaction.
Related Articles:
Synthetic studies on the ingenane diterpenes. Construction of a tetracyclic 8-isoingenane model
[Rigby, James H.; Cuisiat, Stephane V. Journal of Organic Chemistry, 1993 , vol. 58, # 23 p. 6286 - 6291]
New Synthetic Applications of (Bromozinco)-acetonitrile (BrZnCH2CN)
[Orsini, F. Synthesis, 1985 , # 5 p. 500 - 503]