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61.
Wolfgang Werner 《Fresenius' Journal of Analytical Chemistry》1987,328(6):500-501
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We consider a specific continuous-spin Gibbs distribution μt=0 for a double-well potential that allows for ferromagnetic ordering. We study the time-evolution of this initial measure under
independent diffusions.
For `high temperature' initial measures we prove that the time-evoved measure μt is Gibbsian for all t. For `low temperature' initial measures we prove that μt stays Gibbsian for small enough times t, but loses its Gibbsian character for large enough t. In contrast to the analogous situation for discrete-spin Gibbs measures, there is no recovery of the Gibbs property for
large t in the presence of a non-vanishing external magnetic field. All of our results hold for any dimension d≥2. This example suggests more generally that time-evolved continuous-spin models tend to be non-Gibbsian more easily than
their discrete-spin counterparts.
Research carried out at EURANDOM and supported by Deutsche Forschungsgemeinschaft 相似文献
66.
Werner Fudickar 《Tetrahedron》2006,62(46):10639-10646
The photooxygenation of homochiral cyclohexene ketals, which are easily available from 2-cyclohexenone and l-tartrates, affords hydroperoxides and after reduction the corresponding allylic alcohols in good yields and high regioselectivities. This can be rationalized by electronic repulsions in a perepoxide intermediate and provides evidence for unfavorable 1,3 diaxial interactions with a dioxolane oxygen atom. Only low stereoselectivities were observed, due to the flexibility of the cyclohexene ring. However, the diastereomers could be separated and after cleavage of the auxiliary, 4-hydroxy-2-cyclohexen-1-one was isolated in enantiomerically pure form, which can serve as a building block for natural product synthesis. 相似文献
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A palladium-catalyzed parallel synthesis of bis-hetero(aryl) ketones is described with two further synthetic steps allowing easy entry to 3,3-di(hetero)arylpropylamines. 相似文献
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Björn Wängler Carmen Beck Esther Schirrmacher Frank Rösch Michael Eisenhut 《Tetrahedron letters》2006,47(33):5985-5988
The synthesis of tris-allyl-DOTA starting from cyclen and its application in the preparation of DOTA-peptide conjugates is reported. Clinically important conjugates such as DOTA-Tyr3-octreotide (DOTA-TOC), DOTA-Tyr3-octreotate (DOTA-TATE) as well as a DOTA-RGD peptide were synthesized in high yields with Fmoc solid phase peptide synthesis. The final, extremely reliable de-allylation was achieved on solid phase by different methods identifying morpholine/Pd(0) as the most suitable one obtaining all DOTA peptide conjugates in high yields. All DOTA-peptides were purified by reversed phase HPLC and structural identity was proved using MALDI-TOF mass spectrometry. 相似文献
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