79506-64-2Relevant articles and documents
Dealkylative intercepted rearrangement reactions of sulfur ylides
Empel, Claire,Hock, Katharina J.,Koenigs, Rene M.
supporting information, p. 338 - 341 (2019/01/09)
Sulfur ylides are well-known to undergo sigmatropic rearrangement reaction. Herein, we describe a novel reactivity of sulfur ylides, which provides access to the product of a formal functional group metathesis upon dealkylative interception of the rearrangement process. Using a simple iron catalyst and in situ generated diazoalkanes this method provides access to α-mercaptoacetonitrile derivatives.
Acrylonitrile derivatives and pharmaceutical composition cpmprising the same
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Paragraph 0050-0055, (2017/08/02)
The present invention relates to acrylonitrile compounds and pharmaceutical compositions containing the same, and more particularly, to acrylonitrile compounds and pharmaceutical compositions containing the same, which suppress deformation such as oligome
Synthesis of arylthioacetamidoximes as potential antidepressants
Cervena,Hrubantova,Bartosova,Protiva
, p. 1188 - 1198 (2007/10/02)
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