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31.
Dr. Zhoulong Fan Katherine L. Bay Dr. Xiangyang Chen Zhe Zhuang Han Seul Park Dr. Kap-Sun Yeung Prof. Dr. K. N. Houk Prof. Dr. Jin-Quan Yu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(12):4800-4807
A simple and efficient nitrile-directed meta-C−H olefination, acetoxylation, and iodination of biaryl compounds is reported. Compared to the previous approach of installing a complex U-shaped template to achieve a molecular U-turn and assemble the large-sized cyclophane transition state for the remote C−H activation, a synthetically useful phenyl nitrile functional group could also direct remote meta-C−H activation. This reaction provides a useful method for the modification of biaryl compounds because the nitrile group can be readily converted to amines, acids, amides, or other heterocycles. Notably, the remote meta-selectivity of biphenylnitriles could not be expected from previous results with a macrocyclophane nitrile template. DFT computational studies show that a ligand-containing Pd–Ag heterodimeric transition state (TS) favors the desired remote meta-selectivity. Control experiments demonstrate the directing effect of the nitrile group and exclude the possibility of non-directed meta-C−H activation. Substituted 2-pyridone ligands were found to be key in assisting the cleavage of the meta-C−H bond in the concerted metalation–deprotonation (CMD) process. 相似文献
32.
[structure: see text] Thioxo peptide analogues of the alpha-helical peptide GCN4-p1 were synthesized and evaluated for helicity and oligomeric state. Sedimentation equilibrium and CD measurements indicate that the thioxo peptides fold into parallel alpha-helical coiled coil structures essentially identical to the native structure. This work marks the first incorporation of a thioamide linkage into the backbone of an alpha-helix and demonstrates that a thioamide linkage is compatible with positions within the helix as well as near the C-terminus. 相似文献
33.
34.
Saad Alshehri John Burgess Katherine A. Darcey Marttand S. Patel 《Transition Metal Chemistry》1994,19(1):119-122
Summary Solubilities of tris(ethylmaltolato)iron(III) (ethylmaltol = 3-hydroxy-2-ethyl-4-pyrone) were measured in MeOH-H2O, t-BuOH-H2O and diol-H2O mixtures, and in several primary alcohols. Solvation of the ethylmaltol ligand and of two 4-pyridinone analogues has been investigated through solubility measurements in MeOH- H2O and in t-BuOH-H2O mixtures, and in a series of primary alcohols. The solvation characteristics of these compounds are compared with those of the parent maltol, its iron(III) complex and a number of other nonelectrolytes. 相似文献
35.
Crabtree KN Hostetler KJ Munsch TE Neuhaus P Lahti PM Sander W Poole JS 《The Journal of organic chemistry》2008,73(9):3441-3451
The photochemistry of azidopyridine 1-oxides was studied using an array of glass and matrix isolation techniques. As with room temperature, the photochemistry of 4-azidopyridine 1-oxide is dominated by triplet nitrene chemistry. However, in the case of the 3-azide, matrix photolysis indicates the formation of diazabicyclo[4.1.0]hepta-2,4,6-triene N-oxide and diazacycloheptatetraene N-oxide intermediates as well as triplet nitrene. 相似文献
36.
Campbell CD Duguet N Gallagher KA Thomson JE Lindsay AG O'Donoghue AC Smith AD 《Chemical communications (Cambridge, England)》2008,(30):3528-3530
Cascade reaction sequences incorporating N-heterocyclic carbene-based organocatalysis have been developed that allow the direct preparation of a range of (+/-)-4-phenoxycarbonylazlactones in good isolated yields (66-84%) from the corresponding N-p-anisoyl amino acids. 相似文献
37.
Bond length and the electron density at the bond critical point: X--X, Z--Z, and C--Z bonds (X = Li-F, Z = Na-Cl) 总被引:1,自引:0,他引:1
Castillo N Robertson KN Choi SC Boyd RJ Knop O 《Journal of computational chemistry》2008,29(3):367-379
The aim was to investigate the relationship between the bond length and the electron density at the bond critical point in homonuclear X--X and Z--Z and heteronuclear C--Z bonds (X = Li-F, Z = Na-Cl). The d,rho(c) pairs were obtained from 472 target bonds in DFT-optimized (B3LYP/6-311+G(d,p)) small molecular species. These species were selected arbitrarily but with a view to maximize the range widths WR for each atom combination. It was found that (i) with one clear exception, the d(A - A) means (A = X or Z) correlate linearly with the bond lengths d(A(2)) of the respective diatomic molecules; (ii) the d(A - A) means correlate parabolically with n, the formal number of valence electrons in the atoms of the bond; and (iii) with increasing sample size N the ratio WR(rho(c))/WR(d) appears to converge toward a representation f [WR(rho(c))/WR(d)](N-->infinity) characteristic of A. Detailed analysis of the d,rho(c) relationship has shown that by and large simple power regression accounts best for the DFT data. The regression coefficients of d = arho(c) (-b) and rho(c) = alphad(-beta) (b, beta > 0) vary with n in a seemingly irregular manner but one that is consistent with simple chemical notions. The d(A(2)) can be approximated in terms of multilinear MO electron occupancies. 相似文献
38.
Wu X Seo MS Davis KM Lee YM Chen J Cho KB Pushkar YN Nam W 《Journal of the American Chemical Society》2011,133(50):20088-20091
A mononuclear non-heme manganese(IV)-oxo complex has been synthesized and characterized using various spectroscopic methods. The Mn(IV)-oxo complex shows high reactivity in oxidation reactions, such as C-H bond activation, oxidations of olefins, alcohols, sulfides, and aromatic compounds, and N-dealkylation. In C-H bond activation, the Mn(IV)-oxo complex can activate C-H bonds as strong as those in cyclohexane. It is proposed that C-H bond activation by the non-heme Mn(IV)-oxo complex does not occur via an oxygen-rebound mechanism. The electrophilic character of the non-heme Mn(IV)-oxo complex is demonstrated by a large negative ρ value of -4.4 in the oxidation of para-substituted thioanisoles. 相似文献
39.
Olson IA Bacon WA Baez Sosa YY Delaney KM Forte SA Guglielmo MA Hill AN Kiesow KH Langenbacher RE Xun Y Young RO Bowyer WJ 《The journal of physical chemistry. A》2011,115(40):11001-11007
We describe three new strategies for determining heterogeneous reaction rates using photomicroscopy to measure the rate of retreat of metal surfaces: (i) spheres in a stirred solution, (ii) microscopic powder in an unstirred solution, and (iii) spheres on a rotating shaft. The strategies are applied to indium-mediated allylation (IMA), which is a powerful tool for synthetic chemists because of its stereoselectivity, broad applicability, and high yields. The rate-limiting step of IMA, reaction of allyl halides at indium metal surfaces, is shown to be fast, with a minimum value of the heterogeneous rate constant of 1 × 10(-2) cm/s, an order of magnitude faster than the previously determined minimum value. The strategies described here can be applied to any reaction in which the surface is retreating or advancing, thereby broadening the applicability of photomicroscopy to measuring heterogeneous reaction kinetics. 相似文献
40.
Erling Haskjold WencheMarie Olsen Rolf Bjerkens Katherine Kravik 《Photochemistry and photobiology》1993,57(4):663-666
Abstract— The right eyes of 40 rats were exposed to a signal erythemogenic dose fo ultraviolet B irradiation (UVB) at 297nm. The irradiation was directed perpenddicualr to the center of the cornea. The left eyes served as controls. The animals were randomly assigned into 10 groups. The labelling index (LI) after pluse labeling the tritiated thymidine and the mitotic rate (MR) after Colcemid administration were registered in the corneal epithelium at predetermined intervals up to 96 h after the irradiation. A mathematical method was used to corealted corresponding corneal areas from the different animals. In the central the LI was considerably reduced up to 36h after the irradiation. The LI increased toward the peripheral cornea and reached normal values at the limbal area. The MR was also reduced up to 36h. However, this reduction was over the entire epithelium. The block in cell proliferation was followed by increased proliferation. 相似文献