نتایج جستجو برای: staudinger

تعداد نتایج: 421  

2016
C. Schröder G. Klingelhöfer R. V. Morris A. S. Yen F. Renz T. G. Graff

MISSION (ARM): QUANTATIVE IRON MINERALOGY AND OXIDATION STATES. C. Schröder, G. Klingelhöfer, R. V. Morris, A. S. Yen, F. Renz, and T. G. Graff, Biological and Environmental Sciences, University of Stirling, Stirling FK9 4LA, Scotland, UK, [email protected], Institute of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-University, Staudinger Weg 9, 55128 Mainz, Germ...

Journal: :Organic & biomolecular chemistry 2016
Nicola Piens Sven De Craene Jorick Franceus Karen Mollet Kristof Van Hecke Tom Desmet Matthias D'hooghe

cis-3-Acetoxy-4-(3-aryloxiran-2-yl)azetidin-2-ones were prepared through a Staudinger [2+2]-cyclocondensation between acetoxyketene and the appropriate epoxyimines in a highly diastereoselective way. Subsequent potassium carbonate-mediated acetate hydrolysis, followed by intramolecular ring closure through epoxide ring opening, afforded stereodefined 3-aryl-4-hydroxy-2-oxa-6-azabicyclo[3.2.0]he...

2005
G. Klingelhöfer D. S. Rodionov R. V. Morris C. Schröder P. A. de Souza D. W. Ming A. S. Yen B. Bernhardt F. Renz I. Fleischer T. Wdowiak S. W. Squyres

FROM JAROSITE AT MERIDIANI PLANUM TO GOETHITE AT GUSEV CRATER. G. Klingelhöfer, D.S. Rodionov , R.V. Morris, C. Schröder, P.A. de Souza, D.W. Ming, A.S. Yen, B. Bernhardt, F. Renz, I. Fleischer, T. Wdowiak, S.W. Squyres, and the Athena Science Team. Institut für Anorganische und Analytische Chemie, Johannes Gutenberg-Universität, Staudinger Weg 9, D-55128 Mainz, Germany, [email protected]...

Journal: :ACS Catalysis 2021

The traditional Staudinger/aza-Wittig reaction represents one of the most powerful tools for imine formation. However, this multistep procedure, sacrificial phosphine has to be used, resulting in difficulties purification process and waste disposal at same time. Here, we report a redox-neutral azide–alcohol imination methodology enabled by base-metal nickel PN3 pincer catalyst. one-step, waste-...

2013
Diego Carnaroglio Katia Martina Giovanni Palmisano Andrea Penoni Claudia Domini Giancarlo Cravotto

A fast and efficient protocol for the synthesis of N,N'-disubstituted urea derivatives from alkyl halides and primary or secondary amines has been developed. The synthetic pathway combines nucleophilic substitutions and a Staudinger-aza-Wittig reaction in the presence of polymer-bound diphenylphosphine under 14 bar of CO2 pressure and has been performed in a one-pot two-step process. The protoc...

2007
John Nesselroade Peter Molenaar

For more than two decades, the Center for Lifespan Psychology has promoted a perspective on behavioral development that seeks to integrate age periods, domains of functioning, timescales, and levels of analysis. In part through these efforts, lifespan psychology has evolved into a distinct conceptual approach within developmental psychology (e.g., Baltes, 1987; Baltes, Lindenberger, & Staudinge...

Journal: :Organic & biomolecular chemistry 2004
Takamitsu Hosoya Toshiyuki Hiramatsu Takaaki Ikemoto Masayuki Nakanishi Hiroshi Aoyama Ayako Hosoya Tomoya Iwata Kei Maruyama Makoto Endo Masaaki Suzuki

A novel method for radioisotope-free photoaffinity labeling was developed, in which a bifunctional ligand is connected to a target protein by activation of a photoreactive group, such as an aromatic azido or 3-trifluoromethyl-3H-diazirin-3-yl group, and identification of the ligated product is achieved by anchoring of a detectable tag through the Staudinger-Bertozzi reaction with an alkyl azido...

Journal: :Organic & biomolecular chemistry 2008
William P Heal Sasala R Wickramasinghe Robin J Leatherbarrow Edward W Tate

N-Myristoyl transferase-mediated labelling using a substrate modified with an azide or alkyne tag is described as an efficient and site-selective method for the introduction of a bioorthogonal tag at the N-terminus of a recombinant protein. The procedure may be performed in vitro, or in a single over-expression/tagging step in vivo in bacteria; tagged proteins may then be captured using Staudin...

Journal: :iranian journal of science and technology (sciences) 2014
a. jarrahpour

thionyl chloride (or oxalyl chloride) has been used as an efficient and cheap acid activator for one-pot synthesis of β-lactams in good to excellent yields by reaction between imines and acids in the presence of triethylamine at room temperature.

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