98575-68-9Relevant articles and documents
Discovery of Novel N-(4-Hydroxybenzyl)valine Hemoglobin Adducts in Human Blood
Degner, Amanda,Carlsson, Henrik,Karlsson, Isabella,Eriksson, Johan,Pujari, Suresh S.,Tretyakova, Natalia Y.,T?rnqvist, Margareta
, p. 1305 - 1314 (2018/12/11)
Humans are exposed to a wide range of electrophilic compounds present in our diet and environment or formed endogenously as part of normal physiological processes. These electrophiles can modify nucleophilic sites of proteins and DNA to form covalent addu
Supramolecular gelator of gemini type structure and preparation method of supramolecular gelator
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Paragraph 0023; 0024, (2017/02/24)
The invention discloses supramolecular gelator of a gemini type structure and a preparation method of the supramolecular gelator. The preparation method of the supramolecular gelator comprises the following steps that 1, chiral amino acid and aromatic formaldehyde generate an imine reaction and are subjected to reaction to obtain a chiral amino acid arene derivative; 2, the chiral amino acid arene derivative obtained in the step1 and aliphatic long-chain diamine are subjected to amide condensation to obtain the supramolecular gelator of the gemini type structure. The gelator can be prepared into supramolecular gel with multiple metal ions, has the significant responsiveness to outside stimuli such as mechanical stress, pH and temperature and can be applied to the fields of sensors, slow releasing, adsorption and the like.
Resolution of racemic N-benzyl α-amino acids by liquid-liquid extraction: A practical method using a lipophilic chiral cobalt(III) salen complex and mechanistic studies
Dzygiel, Pawel,Reeve, Toby B.,Piarulli, Umberto,Krupicka, Martin,Tvaroska, Igor,Gennari, Cesare
supporting information; experimental part, p. 1253 - 1264 (2009/04/07)
The efficient resolution of racemic N-benzyl α-amino acids (N-Bn-AA) has been achieved by a liquid-liquid extraction process using the lipophilic chiral salen-cobalt(III) complex [CoIII(3)(OAc)]. As a result of the resolution by extraction, one enantiomer (S) of the N-benzyl α-amino acid predominated in the aqueous phase, while the other enantiomer (R) was driven into the organic phase by complexation to cobalt. The complexed amino acid (R) was then quantitatively released by a reductive (CoIII→Co II) counter-extraction with aqueous sodium dithionite or L-ascorbic acid in methanol. The reductive cleavage allowed to recover the [Co II(3)] complex in good yield, which could be easily re-oxidized to [CoIII(3)(OAc)] with air/AcOH and reused with essentially no loss of reactivity and selectivity. Investigation on the nitrogen substitution indicates that the presence of a single benzyl group on the amino acid nitrogen is important to obtain high enantioselectivity in the extraction process. The kinetic vs. thermodynamic nature of the resolution process was also investigated with an enantiomeric exchange experiment, which shows that the liquid-liquid extraction with [CoIII(3)-(OAc)] is an equilibrium process operating under thermodynamic control. In the absence of a suitable crystal structure of the [CoIII(3)(N-Bn-AA)] complexes, computational and spectroscopic studies were used to investigate how the N-benzyl α-amino acids are accommodated in the "binding pocket" of the chiral cobalt complex. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
