103205-23-8Relevant articles and documents
Zinc-mediated addition of bromoacetonitrile to carbonyl compounds under solvent-free conditions
Zhang, Yumei,Du, Xi,An, Bin
, p. 73 - 75 (2014)
Zinc mediated addition reaction of bromoacetonitrile with aryl aldehydes and ketones produces β-hydroxynitriles under solvent-free conditions. The valuable feature of the methodology are solvent-free and catalyst-free conditions and short reaction times (5 min).
Unexpected stereorecognition in nitrilase-catalyzed hydrolysis of β-hydroxy nitriles
Kamila, Sukanta,Zhu, Dunming,Biehl, Edward R.,Hua, Ling
, p. 4429 - 4431 (2007/10/03)
Biocatalytic enantioselective hydrolysis of β-hydroxy nitriles to corresponding (S)-enriched β-hydroxy carboxylic acids has been achieved for the first time by an isolated nitrilase bII6402 from Bradyrhizobium japonicum USDA110. This offers a new "green" approach to optically pure β-hydroxy nitriles and β-hydroxy carboxylic acids. The observed remote stereorecognition is surprising because this nitrilase shows no enantioselectivity for the hydrolysis of α-hydroxy nitriles such as mandelonitrile.