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141.
142.
Madeleine A. Dallaston Christian J. Bettencourt Dr. Sharon Chow Joshua Gebhardt Jordan Spangler Dr. Martin R. Johnston Craig Wall Dr. Jason S. Brusnahan Prof. Craig M. Williams 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(41):9614-9618
Common oxidants used in chemical synthesis, including newly developed perruthenates, were evaluated in the context of understanding (and better appreciating) the sensitiveness and associated potential hazards of these reagents. Analysis using sealed cell differential scanning calorimetry (scDSC) facilitated Yoshida correlations, which were compared to impact sensitiveness and electrostatic discharge experiments (ESD), that enabled sensitiveness ranking. Methyltriphenylphoshonium perruthenate (MTP3, 8 ), isoamyltriphenylphosphonium perruthenate (ATP3, 7 ) and tetraphenylphosphonium perruthenate (TP3, 9 ) were found to be the most sensitive followed by 2-iodoxybenzoic acid (IBX, 2 ) and benzoyl peroxide (BPO, 10 ), whereas the most benign were observed to be Oxone ( 12 ), manganese dioxide (MnO2, 13 ), and N-bromosuccinimide (NBS, 17 ). 相似文献
143.
Molecular dynamics simulations of binary mixtures of benzene, 1,3,5-trifluorobenzene and hexafluorobenzene with dimethylimidazolium hexafluorophosphate were carried out to examine their macroscopic and microscopic properties. The energies and volumes of mixing of these mixtures correlate well with observed microscopic properties including coordination number about the aromatic compound. The local ordering of the ions about an aromatic molecule was found to depend on the quadrupole moment of the aromatic species and to remain qualitatively the same on varying the mole fraction of the aromatic species. Interaction energies showed the most significant interactions to be between the aromatic molecule and the ions located about its equator. These findings have implications for the practical use of ionic liquids as solvents for chemical processes. 相似文献
144.
Jonathan T. Reeves Zhulin Tan Bruce Z. Lu Chris H. Senanayake 《Journal of heterocyclic chemistry》2013,50(3):680-683
Various 2‐formylazoles underwent CuI/sparteine‐catalyzed annulation with 1‐substituted‐4‐iodo‐5‐aminopyrazoles to produce four new heterocyclic ring systems. The reaction was demonstrated for 2‐formylpyrroles, 2‐formylindoles, 2‐formylimidazole, and 3‐methyl‐5‐formylpyrazole. 3‐Substitution of the iodopyrazole was tolerated. 相似文献
145.
Rachael Fay Prof. Dr. Jason P. Holland 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(15):4893-4897
Photochemistry provides a wide range of alternative reagents that hold potential for use in bimolecular functionalisation of proteins. Here, we report the synthesis and characterisation of metal ion binding chelates derivatised with disubstituted tetrazoles for the photoradiochemical labelling of monoclonal antibodies (mAbs). The photophysical properties of tetrazoles featuring extended aromatic systems and auxochromic substituents to tune excitation toward longer wavelengths (365 and 395 nm) were studied. Two photoactivatable chelates based on desferrioxamine B (DFO) and the aza-macrocycle NODAGA were functionalised with a tetrazole and developed for protein labelling with 89Zr, 64Cu and 68Ga radionuclides. DFO-tetrazole ( 1 ) was assessed by direct conjugation to formulated trastuzumab and subsequent radiolabelling with 89Zr. Radiochemical studies and cellular-based binding assays demonstrated that the radiotracer remained stable in vitro retained high immunoreactivity. Positron emission tomography (PET) imaging and biodistribution studies were used to measure the tumour specific uptake and pharmacokinetic profile in mice bearing SK-OV-3 xenografts. Experiments demonstrate that tetrazole-based photochemistry is a viable approach for the light-induced synthesis of PET radiotracers. 相似文献
146.
The use of phase transfer catalysis, PTC, for nucleophillic substitution reactions is well documented.1,2 Included among these reactions is the preparation of both alkyl3 and aryl4 thiocyanates. However, PTC reactions at an acyl carbon are much less common. Brándstróm5 has reported the preparation of acyl azides and Weber6 has used PTC to prepare benzoyl cyanide. Recently Illi7 has used PTC to acylate sterically crowded phenols. 相似文献
147.
A phase transfer catalyst has been used to prepare the title compound and other highly chlorinated compounds from phenylpropanone and carbon tetrachloride. 相似文献
148.
149.
Jan Bouwe van den Berg Jason D. Mireles James Christian Reinhardt 《Journal of Nonlinear Science》2016,26(4):1055-1095
We develop techniques for computing the (un)stable manifold at a hyperbolic equilibrium of an analytic vector field. Our approach is based on the so-called parametrization method for invariant manifolds. A feature of this approach is that it leads to a posteriori analysis of truncation errors which, when combined with careful management of round off errors, yields a mathematically rigorous enclosure of the manifold. The main novelty of the present work is that, by conjugating the dynamics on the manifold to a polynomial rather than a linear vector field, the computer-assisted analysis is successful even in the case when the eigenvalues fail to satisfy non-resonance conditions. This generically occurs in parametrized families of vector fields. As an example, we use the method as a crucial ingredient in a computational existence proof of a connecting orbit in an amplitude equation related to a pattern formation model that features eigenvalue resonances. 相似文献
150.
Christian A. Malapit Donald R. Caldwell Irungu K. Luvaga Dr. Jonathan T. Reeves Dr. Ivan Volchkov Dr. Nina C. Gonnella Dr. Zhengxu S. Han Dr. Carl A. Busacca Prof. Dr. Amy R. Howell Dr. Chris H. Senanayake 《Angewandte Chemie (International ed. in English)》2017,56(24):6999-7002
β-Ketonitriles bearing a quaternary carbon at the 2-position were prepared through Rh-catalyzed addition of aryl boronic acids to 2,2-disubstituted malononitriles. In contrast to the previously described transnitrilative cyanation of aryl boronic acids with dialkylmalononitriles, the present reaction avoids retro-Thorpe collapse of the intermediate addition product through the use of a milder base. The reaction was amenable to a variety of aryl boronic acids and disubstituted malononitriles, providing a diverse array of β-ketonitriles. The products could be further derivatized to valuable chiral α,α-disubstituted-β-aminonitriles through addition reactions to the corresponding N-tert-butanesulfinyl imines. 相似文献