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91.
P. Ackerbauer W. H. Breunlich M. Fuchs S. Fussy M. Jeitler P. Kammel B. Lauss J. Marton W. Prymas J. Werner J. Zmeskal K. Lou C. Petitjean P. Baumann H. Daniel F. J. Hartmann W. Schott T. von Egidy P. Wojciechowski D. Chatellard J. P. Egger E. Jeannet T. Case K. M. Crowe R. H. Sherman V. Markushin 《Hyperfine Interactions》1993,82(1-4):243-258
Complementary to the investigations of the most efficient dt cycle, also the other muon-induced fusion cycles in mixtures of hydrogen isotopes have been studied. The results of these dedicated experiments provide rich information about muon-induced few-body reactions and contribute significantly to a better overall understanding of CF. A summary of the recent progress will be presented. Special emphasis will be put on two characteristic examples, namely a new experimental approach to study the muonic cascade in H-D mixtures and the systematic study of hyperfine effects in muon-induced reactions. 相似文献
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Clayden J Turnbull R Helliwell M Pinto I 《Chemical communications (Cambridge, England)》2004,(21):2430-2431
Thiophene-3-carboxamides bearing allyl or benzyl substituents at nitrogen undergo dearomatising cyclisation on treatment with LDA. Rearrangements transform the dearomatised products into pyrrolinones, azepinones or partially saturated azepinothiophenes. 相似文献
97.
Reacting (−)-menthyl sulfinate with an atropisomeric but racemic aryllithium gives two atropdiastereoisomeric sulfoxides. Separation (by chromatography or crystallisation) and sulfoxide-lithium exchange of each diastereoisomer regenerates the aryllithium in enantiomerically pure form which can be quenched with a range of electrophiles with retention of stereochemical integrity. Overall the reaction sequence is a resolution but without the need for an acidic or basic substituent—a ‘traceless’ method. In certain instances, for example when the nucleophile is an ortholithiated peri-substituted 1-naphthamide, the diastereoisomeric sulfoxides may be interconverted thermally. This allows a dynamic resolution, under thermodynamic control, and hence in principle can give yields of the final products of greater than 50%. The utility of the method is demonstrated by the synthesis of a known atropisomeric phosphine ligand. 相似文献
98.
Martin Fuchs 《manuscripta mathematica》1985,54(1-2):107-119
We minimize the Dirichlet-integral in a class of vector-valued functions u:N defined by Dirichlet-boundary conditions and a side-condition of the form u()M with M bounded and open in N having smooth boundary M. If the boundary values are sufficiently regular we show that the minimizer can only have interior singularities, i.e. the solution is smooth in a neighborhood of . 相似文献
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Frampton MJ Akdas H Cowley AR Rogers JE Slagle JE Fleitz PA Drobizhev M Rebane A Anderson HL 《Organic letters》2005,7(24):5365-5368
[structure: see text] A vinylene-linked porphyrin dimer, with no substituents at the beta-positions, has been synthesized by CuI/CsF promoted Stille coupling. In the crystal structure of this dimer, the C(2)H(2) bridge is twisted by 45 degrees relative to the plane of the porphyrins. The absorption, emission spectra, and electrochemistry reveal substantial porphyrin-porphyrin pi-conjugation. The triplet excited-state absorption spectrum of this dimer makes it suitable for reverse saturable absorption at 710-900 nm. 相似文献