1115-37-3Relevant articles and documents
Straightforward synthesis of 1,2-dicyanoalkanes from nitroalkenes and silyl cyanide mediated by tetrabutylammonium fluoride
Kiyokawa, Kensuke,Nagata, Takaya,Hayakawa, Junpei,Minakata, Satoshi
supporting information, p. 1280 - 1285 (2015/02/19)
A straightforward synthesis of 1,2-dicyanoalkanes by reacting nitroalkenes with trimethylsilyl cyanide in the presence of tetrabutylammonium fluoride is described. The reaction proceeds through a tandem double Michael addition under mild conditions. Employing the hypervalent silicate generated from trimethylsilyl cyanide and tetrabutylammonium fluoride is essential for achieving this transformation. Mechanistic studies suggest that a small amount of water included in the reaction media plays a key role. This protocol is applicable to various types of substrates including electron-rich and electron-deficient aromatic nitroalkenes, and aliphatic nitroalkenes. Moreover, vinyl sulfones were found to be good alternatives, particularly for electron-deficient nitroalkenes. The broad substrate scope and functional group tolerance of the reaction makes this approach a practical method for the synthesis of valuable 1,2-dicyanoalkanes.
REDUCTION OF α - SUBSTITUTED SUCCINONITRILES WITH DIISOBUTYLALUMINIUM HYDRIDE: A FACILE METHOD FOR THE SYNTHESIS OF 3-SUBSTITUTED PYRROLES
Babler, James H.,Spina, Kenneth P.
, p. 1659 - 1660 (2007/10/02)
Treatment of four representative α-substituted succinonitriles (2) with diisobutylaluminium hydride, followed by hydrolysis of each reaction mixture with aqueous sodium dihydrogen phosphate, afford 3-substituted pyrroles (4) in approximately 50percent yie
