35849-02-6Relevant academic research and scientific papers
Silicon and silicon oxide surface modification using thiamine-catalyzed benzoin condensations
Hoop, Kelly A.,Kennedy, David C.,Mishki, Trevor,Lopinski, Gregory P.,Pezacki, John Paul
experimental part, p. 262 - 270 (2012/04/23)
The benzoin condensation that involves the umpolung coupling of two aldehyde groups has been applied to the formation of functionalized silicon and silicon oxide surfaces using thiamine and other N-heterocyclic carbene (NHC) catalysis in water. This bioorthogonal conjugation of an aldehyde to a modified silicon or silicon oxide surface has been monitored and characterized using X-ray photoelectron spectroscopy and IR spectroscopy. NHC catalysis was found to be efficient in water mediating full conversion of the aldehyde functionalized silicon oxide surfaces at the interface.
2-Aroylindoles and 2-aroylbenzofurans with N-hydroxyacrylamide substructures as a novel series of rationally designed histone deacetylase inhibitors
Mahboobi, Siavosh,Sellmer, Andreas,H?cher, Heymo,Garhammer, Christian,Pongratz, Herwig,Maier, Thomas,Ciossek, Thomas,Beckers, Thomas
, p. 4405 - 4418 (2008/02/13)
Histone deacetylase (HDAC) inhibitors are considered to be drugs for targeted cancer therapy and second-generation HDIs are currently being tested in clinical trials. Here, we report on the synthesis and biological evaluation of a novel HDAC inhibitor sca
Novel ampiphilic derivatives of alpha-c-phenyl-n-tert-butyl nitrone
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Page/Page column 6; sheet 3, (2008/06/13)
Novel compounds, derivatives of α-C-phenylN-tert-butyl nitrone, a method for production and use thereof for the preparation of medicaments for the prevention or treatment of diseases related to oxidative stress.
ALUMINA AS AN VERSATILE CATALYST FOR THE SELECTIVE ACETALIZATION OF ALDEHYDES
Kamitori, Yasuhiro,Hojo, Masaru,Masuda, Ryoichi,Yoshida, Tatsushi
, p. 4767 - 4770 (2007/10/02)
Alumina was found to be an effective and convenient catalyst for acetalization of aldehydes to the corresponding 1,3-dioxoranes and 1,3-dioxanes.It can be used for selective protection of only formyl group of ketoaldehydes.
