[reaction: see text]. The total synthesis of the potent immunosuppressant FR901483 is described. In a key step, the intermolecular Diels-Alder cycloaddition of an amidoacrolein with 2-(triisopropylsilyloxy)-1,3-butadiene produced the desired 3-cyclohexene-1-carboxaldehyde. This compound was subjected to basic followed by acidic conditions which effected two sequential aldol cyclizations to deliver the tricyclic ring system of the natural product, suitably functionalized for completion of the total synthesis. 相似文献
The double metallation of 6-bromo-3H-benzothiazol-2-one and 6-bromo-3H-benzoxazol-2-one with methyl magnesium bromide and alkyllithium bases is described. Alkylation with a variety of electrophiles occurs at the 6-position of the heterocycles in good yields. 相似文献
We investigate the instability of one-dimensional dangling-bond (DB) wires fabricated on the H-terminated C(001), Si(001), and Ge(001) surfaces by using density-functional theory calculations. The three DB wires are found to show drastically different couplings between charge, spin, and lattice degrees of freedom, resulting in an insulating ground state. The C DB wire has an antiferromagnetic spin coupling between unpaired DB electrons, caused by strong electron–electron interactions, whereas the Ge DB wire has a strong charge-lattice coupling, yielding a Peierls-like lattice distortion. For the Si DB wire, the antiferromagnetic spin ordering and the Peierls instability are highly competing with each other. The physical origin of such disparate features in the three DB wires can be traced to the different degree of localization of 2p, 3p, and 4p DB orbitals. 相似文献
Solvatochromic vibrational frequency shifts of a few different infrared (IR) probe molecules have been studied by carrying out quantum chemistry calculations for a number of their water clusters. We are particularly focused on the vibrational solvatochromic and electrochromic effects on the CO, CN, and CF stretch modes in carbon monoxide, acetone, 4-cyanopyridine, p-tolunitrile, fluorobenzene, and 3-fluoropyridine. Using multiple interaction site antenna model, we show that their solvatochromic vibrational frequency shifts can be successfully described by considering spatially nonuniform electrostatic potential generated by the surrounding water molecules. It turns out that the CO and CF stretch mode frequencies are approximately proportional to the solvent electric field projected onto the bond axes, whereas the vibrational frequencies of the nitrile stretch mode in 4-cyanopyridine and p-tolunitrile are not. Consequently, it is confirmed that the vibrational Stark tuning rates of the CO and CF stretching modes can be directly used to describe their solvatochromic frequency shifts in condensed phases. However, the nitrile stretch mode frequency shift induced by solvent electrostatic potential appears to be more complicated than its electrochromic phenomenon. To examine the validity of the distributed interaction site model for solvatochromic frequency shifts of these vibrational chromophores, we thus calculated the vibrational Stark tuning rates of the CO, CN, and CF stretch modes and found that they are in good agreement with the experimental results found in literatures. This confirms that a collection of properly chosen distributed interaction sites can be an excellent electric antenna sensing local electrostatics that affects on vibrational frequencies of IR probe modes. 相似文献
A new in situ radioactivity analysis method was developed to determine the fractional contributions of gamma-ray emitters in seawater and sediment from total measured counts. A semi-empirical formula to determine the fractional count contributions was derived using the variation characteristics of the gamma-ray attenuation rate and geometrical efficiency with the measurement points. The proposed method was employed to make in situ gamma-ray measurements using a CeBr3 detector for radioactivity analysis of seawater and sediment at a coastal area with a relatively high tidal range. The full energy peak efficiency of the detector at measurement site was obtained using the GEANT4 simulation code. The radioactivity concentration of 40K in seawater and sediment was determined using the proposed method and laboratory analysis with sampling. The MDA of the in situ measurement for 137Cs and 131I was also estimated assuming they were deposited on the sediment surface-layer. The validation of this method was demonstrated by comparing with the sampling analysis results.
Two new tellurites, NH4RbTe4O9·2H2O and NH4CsTe4O9·2H2O have been synthesized and characterized. The compounds were synthesized hydrothermally, in near quantitative yields, using the alkali metal halide, TeO2, and NH4OH as reagents. The iso-structural materials exhibit layered, two-dimensional structural topologies consisting of TeOx (x=3, 4, or 5) polyhedra separated by NH4+, H2O, Rb+ or Cs+ cations. Unique to these materials is the presence of TeO3, TeO4, and TeO5 polyhedra. Thermogravimetric and infrared spectroscopic data are also presented. Crystal data: NH4RbTe4O9·2H2O: Monoclinic I2/a (no. 15), a=18.917(3) Å, b=6.7002(11) Å, c=21.106(5) Å, β=101.813(2)°, V=2618.5(9) Å3, Z=8; NH4CsTe4O9·2H2O: Monoclinic I2/a (no. 15), a=18.9880(12) Å, b=6.7633(4) Å, c=21.476(2) Å, β=102.3460(10)°, V=2694.2(3) Å3, Z=8. 相似文献