A versatile two-step, one-pot reaction to access N-substituted-2H-indazol-2-amine derivatives has been elaborated. A diverse set of analogues was obtained by a sequential hydrazone formation and reductive cyclization in moderate to good yields from readily available starting materials. The strategy tolerates a broad range of substitutions pattern and functional groups allowing further derivatizations. 相似文献
In the presence of LiBr, a palladium/copper combination catalyzes dehydrogenative amidobrominations of acrylates with NH‐sulfoximines, leading to N‐vinylated products by dual NH/CH coupling, followed by oxidative enamide bromination. Mechanistically, the domino process is proposed to involve palladium(II) species as key intermediates. First synthetic applications of the products have been demonstrated. 相似文献
Merging J?rgensen's and MacMillan's organocatalytic aldehyde chlorinations enables the synthesis of chiral vinylcyclopropanes and (-)-cis-aerangis lactone via terpene-derived 1,2-epoxides. 相似文献
Fluorescent building blocks : Tetracarboxyamides with a central fluorescent diaminoterephthalate unit were prepared from succinyl succinates following a combinatorial‐like strategy. The 2,5‐diaminoterephthalates (see scheme; PG=protecting group) possess four points of diversification and are introduced as new scaffolds for combinatorial chemistry.
We calculate radiative corrections to the flavor-changing neutral current process K→π?+??, both for charged and neutral kaon decays. While the soft-photon approximation is shown to work well for the muon channels, we discuss the necessity of further phase space cuts with electrons in the final state. It is also shown how to transfer our results to other decays such as η→γ?+?? or ω→π0?+??. 相似文献
A new, practical preparation of β,β-dichloroenones in three to four steps allows for a straightforward synthesis of 5-chloropyrazoles. Addition of various propargyl anions to commercially available 4-methyl-4-(trichloromethyl)cyclohexa-2,5-dien-1-one gives high yields of the corresponding propargyl alcohols. These are then transformed, in a single step, via two consecutive rearrangements, a Meyer–Schuster and a (sometimes spontaneous) von Auwers rearomatizing rearrangement, to deliver α,α-aryl-trichloromethylketones. After elimination of HCl, cyclization of the β,β-dichloroenones with various hydrazines delivers 5-chloropyrazoles. The four to five step sequence to 5-chloropyrazoles is very atom economical, expelling only water and two molecules of HCl from all the building blocks. 相似文献
The adsorption of Xe on a Ni(100) surface has been studied in UHV between 30 and 100 K using LEED, thermal desorption spectroscopy (TDS), work function (Δφ) measurements, and UV photoemission (UPS). At and below 80 K, Xe adsorbs readily with high initial sticking probability and via precursor state adsorption kinetics to form a partially ordered phase. This phase has a binding energy of ~5.2 kcal/mole as determined by isosteric heat measurements. The heat of adsorption is fairly constant up to medium coverages and then drops continuously as the coverage increases, indicating repulsive mutual interactions. The thermal desorption is first order with a preexponential factor of about 1012 s?1, indicative of completely mobile adsorption. Adsorbed Xe lowers the work function of the Ni surface by 376 mV at monolayer coverage. (This coverage is determined from LEED to be 5.65 × 1014 Xe molecules/cm-2.) For not too high coverages, θ, Δφ(θ) can be described by the Topping model, with the initial dipole moment μ0 = 0.29 D and the polarizability α being 3.5 × 10?24 cm3. In photoemission, the and orbitals show up as intense peaks at 5.56 and 6.83 eV below Ef which do not shift their position as the coverage varies. Multilayer adsorption (i.e. the filling of the second and third layers) can be seen by TDS. The binding energies of these α states can be estimated to range between 4.5 and 3.5 kcal/mole. The results are compared and contrasted with previous findings of Xe adsorption on other transition metal surfaces and are discussed with respect to the nature of the inert-gas-metal adsorptive bond. 相似文献
Résumé L'utilisation systématique de recuits, contrôlés par des examens radiocristallographiques à températures variables, a permis de faire disparaître les équilibres métastables qui se manifestent entre les hydroxydes de lithium et de sodium. Trois composés sont identifiés avec certitude: 2 LiOH · NaOH, LiOH · NaOH et LiOH · 2 NaOH. Le composé équimolaire est dimorphe, la variété haute température étant de symétrie cubique.
The systematic use of annealing operations controlled by radiocrystallographic examinations at various temperatures permits the elimination of metastable equilibria which occur between lithium and sodium hydroxydes. Three compounds have been characterized with certainty 2 LiOH · NaOH, LiOH · NaOH and LiOH · 2 NaOH. The equimolar compound presents in two crystalline forms: the high-temperature variety crystallizes in the cubic system.
Zusammenfassung Die systematische Anwendung von Prozessen der Wärmebehandlung, welche durch radiokristallographische Untersuchungen bei verschiedenen Temperaturen kontrolliert wurde, ermöglicht den Abbruch der zwischen dem Lithium- und Natriumhydroxid bestehenden metastabilen Gleichgewichte. Drei Verbindungen konnten mit Sicherheit charakterisiert werden: 2 LiOH · NaOH, LiOH · NaOH und LiOH · 2 NaOH. Die äquimolare Verbindung ist dimorph, wobei die bei höherer Temperatur stabile Art eine kubische Symmetrie besitzt.
Silanes are important compounds in industrial and synthetic chemistry. Here, we develop a general approach for the synthesis of disilanes as well as linear and cyclic oligosilanes via the reductive activation of readily available chlorosilanes. The efficient and selective generation of silyl anion intermediates, which are arduous to achieve by other means, allows for the synthesis of various novel oligosilanes by heterocoupling. In particular, this work presents a modular synthesis for a variety of functionalized cyclosilanes, which may give rise to materials with distinct properties from linear silanes but remain challenging synthetic targets. In comparison to the traditional Wurtz coupling, our method features milder conditions and improved chemoselectivity, broadening the functional groups that are compatible in oligosilane preparation. Computational studies support a mechanism whereby differential activation of sterically and electronically distinct chlorosilanes are achieved in an electrochemically driven radical-polar crossover mechanism. 相似文献