نتایج جستجو برای: syntheses

تعداد نتایج: 11788  

Journal: :Inorganic chemistry 2008
Christopher R Graham Richard G Finke

The 88-year-old problem of developing a preferred, optimized synthesis of the prototype Wells-Dawson polyoxometalate, K6[alpha-P2W18O62].14H2O, is addressed herein. Specifically, six published syntheses of K6[alpha-P2W18O62].14H2O are listed and discussed, with emphasis given to the two most recent syntheses, Nadjo and co-workers' 2004 synthesis and a 1997 Inorganic Syntheses procedure by Droeg...

Journal: :Natural product reports 2003
John W Blunt Brent R Copp Robert A Keyzers Murray H G Munro Michèle R Prinsep

Covering: 2016. Previous review: Nat. Prod. Rep., 2017, 34, 235-294This review covers the literature published in 2016 for marine natural products (MNPs), with 757 citations (643 for the period January to December 2016) referring to compounds isolated from marine microorganisms and phytoplankton, green, brown and red algae, sponges, cnidarians, bryozoans, molluscs, tunicates, echinoderms, mangr...

1998
A. Goerdt

We present our numerical code to perform syntheses of galaxy spectra. Our modified linear simplex algorithm has the advantage that no initial solution is required, the non-negativity for the individual contributions is guaranteed, additional spectral components can be added and individual wavelength regions can be weighted. Synthesizing the observed galaxy spectra with isochrone spectra we dete...

Journal: :Pure and applied chemistry. Chimie pure et appliquee 2008
Wen-Hua Chiou Angèle Schoenfelder André Mann Iwao Ojima

Kainic acid, rigidified (S)-glutamic acid, is a well-known kainite receptor agonist for the excitatory transmission in the central nerve system. Our interest in highly selective kainite ligands, prompted us to design a series of new kainic homologues, "homokainoids", i.e., conformationally rigidified (S)-glutamic acids. For the syntheses of enantiopure novel homokainoids (pipecolinoglutamic aci...

Journal: :The Journal of biological chemistry 1990
H C Canter Cremers M Batley J W Redmond L Eydems M W Breedveld L P Zevehuizen E Pees C A Wijffelman B J Lugtenberg

Rhizobium leguminosarum bv. viciae Exo- mutant strains RBL5523,exo7::Tn5,RBL5523,exo8::Tn5 and RBL5523,exo52::Tn5 are affected in nodulation and in the syntheses of lipopolysaccharide, capsular polysaccharide, and exocellular polysaccharide. These mutants were complemented for nodulation and for the syntheses of these polysaccharides by plasmid pMP2603. The gene in which these mutants are defec...

Journal: :Molecules 2011
Christian Förster Maik Schubert Hans-Jürgen Pietzsch Jörg Steinbach

Two basic and simple synthetic routes for mono- and bis-maleimide bearing 1,4,7-triazacyclononane-N,N',N''-triacetic acid (NOTA) chelators as new bifunctional chelators are described. The syntheses are characterized by their simplicity and short reaction times, as well as practical purification methods and acceptable to very good chemical yields. The usefulness of these two synthetic pathways i...

Journal: :Tetrahedron 2010
David E White Ian C Stewart Brinton A Seashore-Ludlow Robert H Grubbs Brian M Stoltz

Described in this report is an enantioselective route toward the chamigrene natural product family. The key disconnections in our synthetic approach include sequential enantioselective decarboxylative allylation and ring-closing olefin metathesis to form the all-carbon quaternary stereocenter and spirocyclic core present in all members of this class of compounds. The generality of this strategy...

Journal: :Chemistry 2002
Marco Eissen Jürgen O Metzger

A simple quantitative approach to enable chemists to compare alternative chemical syntheses on the lab bench with respect to their resource usage and their potential environmental impact is proposed; this may be useful for the systematic design of more sustainable processes. We consider as metrics the mass index S(-1) and the environmental factor E to characterize quantitatively the reaction in...

Journal: :The Journal of organic chemistry 2014
Sunkyu Han Karen C Morrison Paul J Hergenrother Mohammad Movassaghi

A full account of our concise and enantioselective total syntheses of all known (-)-trigonoliimine alkaloids is described. Our retrobiosynthetic analysis of these natural products enabled identification of a single bistryptamine precursor as a precursor to all known trigonoliimines through a sequence of transformations involving asymmetric oxidation and reorganization. Our enantioselective synt...

2017
David A Russell Julien J Freudenreich Joe J Ciardiello Hannah F Sore David R Spring

We describe stereocontrolled semi-syntheses of deguelin and tephrosin, anti-cancer rotenoids isolated from Tephrosia vogelii. Firstly, we present a new two-step transformation of rotenone into rot-2'-enonic acid via a zinc-mediated ring opening of rotenone hydrobromide. Secondly, following conversion of rot-2'-enonic acid into deguelin, a chromium-mediated hydroxylation provides tephrosin as a ...

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