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Stereochemistry studies

Adamantane can be used to construct peptidic scaffolding and synthesis of artificial proteins. It has been introduced into different types of synthetic peptidic macrocycles, which are useful tools in peptide chemistry and stereochemistry studies and have many other applications as well. Introduction of amino acid-functionalized adamantane to the DNA nanostmctures might lead to construction of DNA-adamantane-amino acid nanostmctures with desirable stiffness and integrity. Diamondoids can be employed to constmct molecular rods, cages, and containers and also for utilization in different methods of self-assembly. In fact, through the development of self-assembly approaches and utilization of diamondoids in these processes, it would be possible to design and constmct novel nanostmctures for effective and specific carriers for each dmg. [Pg.249]

Previous work has shown that the electronic characteristics of the benzene substituent in triarylphosphine chlororhodium complexes have a marked influence on the rate of olefin hydrogenation catalyzed by these compounds. Thus, in the hydrogenation of cyclohexene using L3RhCl the rate decreased as L = tri-p-methoxyphenylphosphine > triphenylphosphine > tri-p-fluorophenylphosphine (14). In the hydrogenation of 1-hexene with catalysts prepared by treating dicyclooctene rhodium chloride with 2.2-2.5 equivalents of substituted triarylphosphines, the substituent effect on the rate was p-methoxy > p-methyl >> p-chloro (15). No mention could be found of any product stereochemistry studies using this type of catalyst. [Pg.125]

A variety of 10-aryl <03EJ02098> and IO-CF3 <03JOC9763> derivatives of dihydroartemisinin and 9-substituted derivatives of artemisinin <03JMC4244> have been synthesised and their reactions and stereochemistry studied. [Pg.423]

Acetylenic derivatives of 2,5-dimethyl-1-phenylphos-phorinane 1-oxide and 1-sulphide have been synthesized and their stereochemistry studied (B.M. Butin et at., Izv. Akad. Nauk Kaz. SSR, Khim., 1977, 49). [Pg.115]

If you rotate the molecule 180° you will have the same apparent stereochemistry. Study this drawing until you can see for yourself that it is true, and if you have a modeling kit to be able to construct this molecule then the symmetry will be very apparent. [Pg.67]

Methyl and simple alkyl radicals are essentially planar with sp2 hybridization and the single electron in a p orbital, in contrast to the analogous silyl radicals which are pyramidal with approximately sp3 hybridization for all the valence orbitals three bonding and one singly occupied. The evidence is for this comes from ESR and stereochemistry studies. [Pg.128]

Although the stereochemistry studies discussed above were not completely definitive, the doubt cast on the author s original suggestion of syn hydroxypalladation required further... [Pg.483]

Organometallics Studied Using Mass Spectrometry Peptides and Proteins Studied Using Mass Spectrometry SIFT Applications in Mass David Smith and Patrik Spectrometry Stereochemistry Studied Using Mass Spectrometry... [Pg.43]

See also Field Ionization Kinetics in Mass Spectrometry Fragmentation in Mass Spectrometry Ion Dissociation Kinetics, Mass Spectrometry Ion Structures in Mass Spectrometry Ionization Theory Isotopic Labelling in Mass Spectrometry Metastable Ions MS-MS and MS" Sector Mass Spectrometers Statistical Theory of Mass Spectra Stereochemistry Studied Using Mass Spectrometry. [Pg.548]

See also Fragmentation in Mass Spectrometry Hydrogen Bonding and other Physicochemical Interactions Studied By IR and Raman Spectroscopy Ion Collision Theory Ion Energetics in Mass Spectrometry Ion Molecule Reactions in Mass Spectrometry Metastable Ions Negative Ion Mass Spectrometry, Methods Neutralization-Reionization in Mass Spectrometry Proton Affinities Sector Mass Spectrometers Stereochemistry Studied Using Mass Spectrometry. [Pg.999]

See also Biochemical Applications of Mass Spectrometry Chromatography-MS, Methods Cosmo-chemical Applications Using Mass Spectrometry Food Science, Applications of Mass Spectrometry Fragmentation in Mass Spectrometry Isotope Ratio Studies Using Mass Spectrometry Labelling Studies in Biochemistry Using NMR Medical Science Applications of IR MS-MS and MS" Metastable Ions Sector Mass Spectrometers Stereochemistry Studied Using Mass Spectrometry. [Pg.1095]


See other pages where Stereochemistry studies is mentioned: [Pg.223]    [Pg.95]    [Pg.58]    [Pg.250]    [Pg.29]    [Pg.1327]    [Pg.354]    [Pg.54]    [Pg.481]    [Pg.23]    [Pg.801]    [Pg.1045]    [Pg.1045]    [Pg.1046]    [Pg.1047]    [Pg.1048]    [Pg.1049]    [Pg.1050]    [Pg.1051]    [Pg.1052]    [Pg.1053]    [Pg.1054]    [Pg.1055]    [Pg.1056]    [Pg.1057]    [Pg.1201]    [Pg.1230]   


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