tempo and azobis(isobutyronitrile)

tempo has been researched along with azobis(isobutyronitrile)* in 1 studies

Other Studies

1 other study(ies) available for tempo and azobis(isobutyronitrile)

Article	Year
Copper-catalyzed cyanation of disulfides by azobisisobutyronitrile leading to thiocyanates. Chemical communications (Cambridge, England), 2014, Oct-18, Volume: 50, Issue:81 The copper-catalyzed cyanation of disulfides by azobisisobutyronitrile (AIBN) was developed, leading to thiocyanates in moderate to good yields. This procedure tolerates a series of functional groups, such as chloro, nitro, methyl and methoxycarbonyl in the phenyl ring of disulfides. Notably, it enables the use of two ArS units in (ArS)2. CuI was found to be essential for the in situ formation of cyanide anions. Topics: Anions; Catalysis; Copper; Cyanides; Cyclic N-Oxides; Disulfides; Gas Chromatography-Mass Spectrometry; Nitriles; Thiocyanates	2014

Article

Year

Copper-catalyzed cyanation of disulfides by azobisisobutyronitrile leading to thiocyanates.

Chemical communications (Cambridge, England), 2014, Oct-18, Volume: 50, Issue:81

The copper-catalyzed cyanation of disulfides by azobisisobutyronitrile (AIBN) was developed, leading to thiocyanates in moderate to good yields. This procedure tolerates a series of functional groups, such as chloro, nitro, methyl and methoxycarbonyl in the phenyl ring of disulfides. Notably, it enables the use of two ArS units in (ArS)2. CuI was found to be essential for the in situ formation of cyanide anions.

Topics: Anions; Catalysis; Copper; Cyanides; Cyclic N-Oxides; Disulfides; Gas Chromatography-Mass Spectrometry; Nitriles; Thiocyanates

2014