34661-16-0Relevant academic research and scientific papers
Triorganotin(IV) complexes with o-substituted arylhydroxamates: Synthesis, spectroscopic characterization, X-ray structures and in vitro cytotoxic activities
Khan, Naqeebullah,Farina, Yang,Mun, Lo Kong,Rajab, Nor Fadilah,Awang, Normah
, p. 26 - 33 (2014/05/20)
Six new triorganotin(IV) complexes with six different RN-2-X- benzohydroxamic acid ligands having general formula R′C(O)N(RN)OH (R′ = alkyl/aryl; RN = alkyl/aryl or H), (X = -I, -NO2, -OCH3, -Br and R = -CH3, -C6/sub
Benzaldehyde lyase-catalyzed direct amidation of aldehydes with nitroso compounds
Ayhan, Peruze,Demir, Ayhan S.
supporting information; experimental part, p. 624 - 629 (2011/04/24)
Benzaldehyde lyase from the Pseudomonas fluorescens catalyzes the reaction of aromatic aldehydes with nitroso compounds and furnishes N-arylhydroxamic acids in high yields. Aromatic aldehydes and benzoins are converted into enamine-carbanion-like intermediates prior to their reaction with nitroso compounds. The kinetic resolution of rac-2-hydroxy-1,2-diphenylethanones furnished (S)-benzoins and arylhydroxamic acids with high enantioselectivities and conversions.
Acylation of Amines and Alcohols by Anodic Oxidation of N-Phenyl-hydroxamic Acids
Masui, Masaichiro,Ueshima, Takahiro,Yamazaki, Tomoko,Ozaki, Shigeko
, p. 2130 - 2133 (2007/10/02)
The electrochemical acylation of amines and alcohols is described.The yield of products from the electrochemical reaction is markedly improved by the use of N-phenyl derivatives of hydroxamic acids in place of the N-hydrogen counterparts.Keywords - anodic oxidation; acylation of amine and alcohol; N-phenylhydroxamic acid; acetonitrile; glassy-carbon electrode
