71189-74-7Relevant articles and documents
Cyanosilylation of prochiral ketones catalyzed by lanthanide complexes
Mei, Luo,Zhu, Ma Huai
, p. 2615 - 2623 (2005)
A new series of silylene-bridged rare-earth complexes involving fluorenyl are shown to be the very efficient Lewis acid catalysts, giving some cyano trimethylsilyl ethers of ketones in >99% yields. Copyright Taylor & Francis, Inc.
Enantioselective cyanosilylation of ketones with amino acid/BINAP/ ruthenium(II)-lithium phenoxide catalyst systems
Uemura, Masato,Kurono, Nobuhito,Sakai, Yusuke,Ohkuma, Takeshi
supporting information; experimental part, p. 2023 - 2030 (2012/10/23)
Enantioselective reactions of simple ketones, α,α- and β,β-dialkoxy ketones, and α-alkoxy ketones with trimethylsilyl cyanide catalyzed by the bimetallic systems of amino acid/BINAP/ruthenium(II) complexes and lithium phenoxide have been studied [BINAP=2,
Construction of tetrasubstituted carbon by an organocatalyst: Cyanation reaction of ketones and ketimines catalyzed by a nucleophilic N-heterocyclic carbene
Fukuda, Yoshimasa,Kondo, Kazuhiro,Aoyama, Toyohiko
, p. 2649 - 2652 (2008/02/04)
A method for cyanation reaction of ketones and ketimines having lower reactivity than aldehydes and aldimines with TMSCN in the presence of N-heterocyclic carbene prepared from 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride and potassium tert-butoxide
