Enantioselective cyanosilylation of aldehydes catalyzed by novel camphor derived Schiff bases-titanium(IV) complexes
作者:Ewelina Błocka、Mariusz J. Bosiak、Mirosław Wełniak、Agnieszka Ludwiczak、Andrzej Wojtczak
DOI:10.1016/j.tetasy.2014.03.001
日期:2014.4
Five tridentate Schiff bases have been prepared from (1R,2S,3R,4S)-3-amino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol and salicylaldehydes. X-ray structure investigation revealed differences in their molecular conformation, and their titanium(IV) complexes have been studied with NMR techniques. Among them the complex with the Schiffbase obtained from 2-hydroxy-3-isopropylbenzaldehyde, is the most selective
A new (R)-hydroxynitrile lyase from Prunus mume: asymmetric synthesis of cyanohydrins
作者:Samik Nanda、Yasuo Kato、Yasuhisa Asano
DOI:10.1016/j.tet.2005.08.105
日期:2005.11
A new hydroxynitrile lyase (HNL) was isolated from the seed of Japanese apricot (Prunus mume). The enzyme has similar properties with HNL isolated from other Prunus species and is FAD containing enzyme. It accepts a large number of unnatural substrates (benzaldehyde and its variant) for the addition of HCN to produce the corresponding cyanohydrins in excellent optical and chemical yields. A new HPLC