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71.
Maren Bulmahn 《Nachrichten aus der Chemie》2008,56(4):443-444
72.
Hoffmann Holger Knizia Christian Kuhne Maren Panne Ulrich Schneider Rudolf J. 《Accreditation and quality assurance》2018,23(6):349-364
Accreditation and Quality Assurance - Estrone (E1), a metabolite of the estrogenic hormones 17β-estradiol (β-E2) and 17α-estradiol (α-E2), is itself a potent estrogen which can... 相似文献
73.
Active Intracellular Delivery of a Cas9/sgRNA Complex Using Ultrasound‐Propelled Nanomotors
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Malthe Hansen‐Bruhn Dr. Berta Esteban‐Fernández de Ávila Dr. Mara Beltrán‐Gastélum Prof. Jing Zhao Dr. Doris E. Ramírez‐Herrera Pavimol Angsantikul Prof. Kurt Vesterager Gothelf Prof. Liangfang Zhang Prof. Joseph Wang 《Angewandte Chemie (International ed. in English)》2018,57(10):2657-2661
Direct and rapid intracellular delivery of a functional Cas9/sgRNA complex using ultrasound‐powered nanomotors is reported. The Cas9/sgRNA complex is loaded onto the nanomotor surface through a reversible disulfide linkage. A 5 min ultrasound treatment enables the Cas9/sgRNA‐loaded nanomotors to directly penetrate through the plasma membrane of GFP‐expressing B16F10 cells. The Cas9/sgRNA is released inside the cells to achieve highly effective GFP gene knockout. The acoustic Cas9/sgRNA‐loaded nanomotors display more than 80 % GFP knockout within 2 h of cell incubation compared to 30 % knockout using static nanowires. More impressively, the nanomotors enable highly efficient knockout with just 0.6 nm of the Cas9/sgRNA complex. This nanomotor‐based intracellular delivery method thus offers an attractive route to overcome physiological barriers for intracellular delivery of functional proteins and RNAs, thus indicating considerable promise for highly efficient therapeutic applications. 相似文献
74.
Inside Cover: Active Intracellular Delivery of a Cas9/sgRNA Complex Using Ultrasound‐Propelled Nanomotors (Angew. Chem. Int. Ed. 10/2018)
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76.
Dr. Raheleh Pourkaveh Ass. Prof. Dr. Maren Podewitz Prof. Dr. Michael Schnürch 《European journal of organic chemistry》2023,26(8):e202201179
Herein we report, a rhodium-catalyzed Fujiwara-Moritani-type reaction of unactivated terminal alkenes and benzoic acid derivatives bearing electron donating residues under mild conditions. The acid functionality acts as a traceless directing group delivering products alkenylated in meta-position to the electron donating substituent in contrast to the usually obtained ortho- and para-substitution in Friedel-Crafts-type reactions. Remarkably, the new C−C bond is formed to the C2 of the terminal olefin, in contrast to similar reported transformations. Initially formed mixtures of exo- and endo-double bond isomers can be efficiently isomerized to the more stable endo-products. 相似文献
77.
Armando Berlanga-Vázquez Radu A. Talmazan Carlos A. Reyes-Mata Prof. Edmundo G. Percástegui Dr. Marcos Flores-Alamo Prof. Maren Podewitz Prof. Ivan Castillo 《欧洲无机化学杂志》2023,26(6):e202200596
Functionalization of the phenolic rim of p-tert-butylcalix[8]arene with phenanthroline to create a cavity leads to formation of two regioisomers. Substitution of positions 1 and 5 produces the known C2v-symmetric regioisomer 1,5-(2,9-dimethyl-1,10-phenanthroyl)-p-tert-butylcalix[8]arene ( L1,5 ), while substitution of positions 1 and 4 produces the Cs-symmetric regioisomer 1,4-(2,9-dimethyl-1,10-phenanthroyl)-p-tert-butylcalix[8]arene ( L1,4 ) described herein. [ Cu(L1,4)I ] was synthesized from L1,4 and CuI in good yield and characterized spectroscopically. To evaluate the effect of its cavity on catalysis, Ullmann-type C−S coupling was chosen as proof-of-concept. Selected aryl halides were used, and the results compared with the previously reported Cu(I)/ L1,5 system. Only highly activated aryl halides generate the C−S coupling product in moderate yields with the Cu(I)/ L1,4 system. To shed light on these observations, detailed computational investigations were carried out, revealing the influence of the calix[8]arene macrocyclic morphology on the accessible conformations. The L1,4 regioisomer undergoes a deformation that does not occur with L1,5 , resulting in an exposed catalytic center, presumably the cause of the low activity of the former system. The 1,4-connectivity was confirmed in the solid-state structure of the byproduct [ Cu(L1,4 − H) (CH3CN)2] that features Cu(I) coordinated inside a cleft defined by the macrocyclic framework. 相似文献
78.
79.
The COSY-TOF Collaboration S.?Jowzaee E.?Borodina H.?Clement E.?Doroshkevich R.?Dzhygadlo K.?Ehrhardt W.?Eyrich W.?Gast A.?Gillitzer D.?Grzonka F.?Hauenstein P.?Klaja L.?Kober K.?Kilian M.?Krapp M.?Mertens P.?Moskal J.?Ritman E.?RoderburgEmail author M.?R?der W.?Schroeder T.?Sefzick J.?Smyrski P.?Wintz P.?Wüstner 《The European Physical Journal A - Hadrons and Nuclei》2016,52(1):7
80.
In this study the temperature stability of several normal phase and RP columns was investigated using a water-only mobile phase. The temperature was adjusted to 120 degrees C for the bare silica stationary phases and to 185 degrees C for the metal oxide and carbon stationary phases. It could be shown that metal oxide stationary phases exhibited excellent thermal stability over the duration of the test period and are therefore suitable for high temperature LC applications. 相似文献