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141.
142.
Richard Ian Cooper David John Watkin Howard D. Flack 《Acta Crystallographica. Section C, Structural Chemistry》2016,72(4):261-267
A study of post‐refinement absolute structure determination using previously published data was carried out using the CRYSTALS software package. We show that absolute structure determination may be carried out optimally using the analyses available in CRYSTALS, and that it is not necessary to have the separate procedures absolute structure determination and no interest in absolute structure as proposed by Flack [Chimia (2014), 68 , 26–30]. 相似文献
143.
144.
We use ending laminations for Weil–Petersson geodesics to establish that bounded geometry is equivalent to bounded combinatorics
for Weil–Petersson geodesic segments, rays, and lines. Further, a more general notion of non-annular bounded combinatorics, which allows arbitrarily large Dehn-twisting, corresponds to an equivalent condition for Weil–Petersson geodesics. As an
application, we show theWeil–Petersson geodesic flow has compact invariant subsets with arbitrarily large topological entropy. 相似文献
145.
Alfonso Gracia-Saz Kirill Charles Howard Mackenzie 《Letters in Mathematical Physics》2009,90(1-3):175-200
We calculate the group of dualization operations for triple vector bundles, showing that it has order 96 and not 72 as given in Mackenzie’s original treatment. The group is a nonsplit extension of S 4 by the Klein group. Dualization operations are interpreted as functors on appropriate categories and are said to be equal if they are naturally isomorphic. The method set out here will be applied in a subsequent paper to the case of n-fold vector bundles. 相似文献
146.
147.
Dr. Kim Søholm Halskov Dr. Howard S. Roth Prof. Dr. Jonathan A. Ellman 《Angewandte Chemie (International ed. in English)》2017,56(31):9183-9187
The first syntheses of privileged [5,6]-bicyclic heterocycles, with ring-junction nitrogen atoms, by transition metal catalyzed C−H functionalization of C-alkenyl azoles is disclosed. Several reactions are applied to alkenyl imidazoles, pyrazoles, and triazoles to provide products with nitrogen incorporated at different sites. Alkyne and diazoketone coupling partners give azolopyridines with various substitution patterns. In addition, 1,4,2-dioxazolone coupling partners yield azolopyrimidines. Furthermore, the mechanisms for the reactions are discussed and the utility of the developed approach is demonstrated by iterative application of C−H functionalization for the rapid synthesis of a patented drug candidate. 相似文献
148.
We prove that, for 3g–3+n>1 and (g,n)(1,2), the group of Weil–Petersson isometries of the Teichmüller space T
g,n
coincides with the extended mapping class group. 相似文献
149.
Saxon E Luchansky SJ Hang HC Yu C Lee SC Bertozzi CR 《Journal of the American Chemical Society》2002,124(50):14893-14902
The structure of sialic acid on living cells can be modulated by metabolism of unnatural biosynthetic precursors. Here we investigate the conversion of a panel of azide-functionalized mannosamine and glucosamine derivatives into cell-surface sialosides. A key tool in this study is the Staudinger ligation, a highly selective reaction between modified triarylphosphines and azides that produces an amide-linked product. A preliminary study of the mechanism of this reaction, and refined conditions for its in vivo execution, are reported. The reaction provided a means to label the glycoconjugate-bound azidosugars with biochemical probes. Finally, we demonstrate that the cell-surface Staudinger ligation is compatible with hydrazone formation from metabolically introduced ketones. These two strategies provide a means to selectively modify cell-surface glycans with exogenous probes. 相似文献
150.