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[structures: see text] The total syntheses of the amaryllidaceae alkaloids haemanthidine, pretazettine, and tazettine as optically pure enantiomers are reported. Using D-mannose as the starting material, the critical relative stereochemical relationships are established with an intramolecular nitrone-alkene cycloaddition reaction. The synthetic route leads successively to (-)-haemanthidine and then to (+)-pretazettine and (+)-tazettine, taking advantage of the well-established complex relationships among these three alkaloids. 相似文献
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[structure: see text] A new series of ligands with a novel phosphine-aminophosphine ligation design as depicted in structure 1 has been prepared on a ferrocenylethyl backbone. These BoPhoz ligands of structure 2 have afforded exceedingly high activity and enantioselectivity in the rhodium-catalyzed asymmetric hydrogenation of dehydro-alpha-amino acid derivatives, itaconic acids, and alpha-ketoesters. These air-stable ligands are readily prepared from cost-effective and non-pyrophoric intermediates. 相似文献
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H. Karami J. Carr N.C. Debenham D.A. Garbutt W.G. Jones D.M. Binnie J. Keyne P. Moissidis H.N. Sarma I. Siotis 《Nuclear Physics B》1979,154(3):503-518
Measurements are reported of the differential cross section for the reaction π?+p→ω+n from threshold to a final-state c.m. momentum . The previously reported fall in total cross section below about 100 MeV/c is again seen. The differential cross section remains close to isotropic over the entire range. A paralle experiment on the variation in the elastic differential cross section across the threshold shows evidence of this threshold. The elastic data cover a range of incident moments from 1010 to 1180 MeV/c in steps of 5 MeV/c. 相似文献
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Duygu İNCİ 《应用有机金属化学》2020,34(12):e6016
NOO-type tridentate Schiff base, N-salicylidene-2-aminobenzoic acid, (H2L), and its ternary Cu (II) complex containing H2L Schiff base and 4,7-dimethyl-1,10-phenanthroline (4,7-dmphen), [Cu(4,7-dmphen)(H2L)]27H2O, have been synthesized and characterized by CHN analysis, ESI-MS, FTIR, and single-crystal X-ray diffraction techniques. The interaction of alone H2L Schiff base ligand and ternary Cu (II) complex with biomacramolecules {calf thymus DNA (CT-DNA) and bovine serum albumin (BSA)} has been investigated by electronic absorption and fluorescence spectroscopy. The experimental results indicate that H2L Schiff base ligand and ternary Cu (II) complex bind to CT-DNA by means of a moderate intercalation mode. Furthermore, the fluorescence quenching mechanism between H2L Schiff base ligand and ternary Cu (II) complex with BSA possesses a static quenching process. Radical scavenging activity of H2L Schiff base ligand and ternary Cu (II) complex was measured in terms of EC50, using the DPPH and H2O2 methods. Biomacromolecule interactions and scavenging activity studies revealed that ternary Cu (II) complex yielded better results than H2L Schiff base ligand alone. 相似文献
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A. Ertoprak B. Cederwall C. Qi M. Doncel U. Jakobsson B. M. Nyakó G. Jaworski P. Davies G. de France I. Kuti D. R. Napoli R. Wadsworth S. S. Ghugre R. Raut B. Akkus H. Al Azri A. Algora G. de Angelis A. Atac T. Bäck A. Boso E. Clément D. M. Debenham Zs. Dombrádi S. Ertürk A. Gadea F. Ghazi Moradi A. Gottardo T. Hüyük E. Ideguchi H. Li C. Michelagnoli V. Modamio J. Nyberg M. Palacz C. M. Petrache F. Recchia M. Sandzelius M. Siciliano J. Timár J. J. Valiente-Dobón Z. G. Xiao 《The European Physical Journal A - Hadrons and Nuclei》2018,54(9):145
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Boaz NW Mackenzie EB Debenham SD Large SE Ponasik JA 《The Journal of organic chemistry》2005,70(5):1872-1880
A new class of bidentate ligands utilizing a phosphine-aminophosphine structure has been prepared on a ferrocenylethyl backbone in a straightforward and scalable fashion from acetylferrocene. The unique property of the alpha-ferrocenyl carbonium ion that allows the replacement of a variety of "leaving groups" with retention of configuration greatly facilitates the synthesis, and a number of ligands have been prepared by varying the nitrogen and phosphorus substituents on the aminophosphine. These readily prepared phosphinoferrocenylaminophosphines, known as BoPhoz ligands, show surprising hydrolytic and air stability, with no degradation after 3 years open to the air. The rhodium complexes of these ligands show exceedingly high enantioselectivities (generally >95% ee) and activities often in excess of 50,000 catalyst turnovers per hour for the asymmetric hydrogenation of a wide variety of dehydro-alpha-amino acid and itaconic acid derivatives. They also show high activity and good to excellent enantioselectivity for the hydrogenation of a number of alpha-ketoesters. 相似文献
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