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71.
An acyl iminium ion-initiated tandem cyclization gave an unexpected dienone product, a seco-azasteroid (2). The factors governing the formation of 2 were investigated in an attempt to optimize its formation. The reaction was applied to a more elaborate system, resulting in the synthesis of the full steroid skeleton of 13-azaandrosta-1,4-diene-3,17-dione (3), which contains the unusual substitution of a chlorine atom for the axial 19-methyl. 相似文献
72.
Approximate formulas for the transverse-relaxation rate constant and resonance frequency have been derived for nuclear spins subject to two-site chemical exchange. The new results are more accurate than previous approximations when chemical exchange does not approach the fast-exchange limit or when site populations are not highly asymmetric. Results are derived from an effective average evolution operator that contains contributions from both exact eigenvalues of the Bloch-McConnell equations. These expressions are useful for interpretation of chemical exchange processes in NMR spectroscopy. 相似文献
73.
Dragana TadicJoannes T.M Linders Judith L Flippen-Anderson Arthur E JacobsonKenner C Rice 《Tetrahedron》2003,59(25):4603-4614
Two of the 12 possible oxide-bridged phenylmorphans, were synthesized, rac-(3R,6aS,11aS)-2-methyl-1,3,4,5,6,11a-hexahydro-2H-3,6a-methanobenzofuro[2,3-c]azocine-10-ol (7) (the ortho-c compound), and rac-(3R,6aS,11aS)-2-methyl-1,3,4,5,6,11a-hexahydro-2H-3,6a-methanobenzofuro[2,3-c]azocine-8-ol (8) (the para-c compound). Single-crystal X-ray diffraction studies indicated that the dihedral angle between the least squares planes through the phenyl ring and the atoms C1, C11a, C12, and C3 in the piperidine ring in both 7·CHCl3 and 8·HBr was 6.9°. The C12-C6a-C6b-C10a torsion angle was found to be 139.3° for both compounds. The angular relationship between the phenolic ring and the piperidine ring in phenylmorphans that interact with specific opioid receptors as agonists or antagonists is of considerable theoretical interest. 相似文献
74.
New quaternary intermetallic phases REMGa(3)Ge (1) (RE = Y, Sm, Tb, Gd, Er, Tm; M = Ni, Co) and RE(3)Ni(3)Ga(8)Ge(3) (2) (RE = Sm, Gd) were obtained from exploratory reactions involving rare-earth elements (RE), transition metal (M), Ge, and excess liquid Ga the reactive solvent. The crystal structures were solved with single-crystal X-ray and electron diffraction. The crystals of 1 and 2 are tetragonal. Single-crystal X-ray data: YNiGa(3)Ge, a = 4.1748(10) A, c = 23.710(8) A, V = 413.24(2) A(3), I4/mmm, Z = 4; Gd(3)Ni(3)Ga(8)Ge(3), a = 4.1809(18) A, c = 17.035(11) A, V = 297.8(3) A(3), P4/mmm, Z = 1. Both compounds feature square nets of Ga atoms. The distribution of Ga and Ge atoms in the REMGa(3)Ge was determined with neutron diffraction. The neutron experiments revealed that in 1 the Ge atoms are specifically located at the 4e crystallographic site, while Ga atoms are at 4d and 8g. The crystal structures of these compounds are related and could be derived from the consecutive stacking of disordered [MGa](2) puckered layers, monatomic RE-Ge planes and [MGa(4)Ge(2)] slabs. Complex superstructures with modulations occurring in the ab-plane and believed to be associated with the square nets of Ga atoms were found by electron diffraction. The magnetic measurements show antiferromagnetic ordering of the moments located on the RE atoms at low temperature, and Curie-Weiss behavior at higher temperatures with the values of mu(eff) close to those expected for RE(3+) free ions. 相似文献
75.
The preparation of some new cationic aryldiazo complexes of platinum of formula trans-[Pt(N2Ar)(PEt3)2L]+, where N2Ar = N2C6H4F-m or -p and L = NH3, Py, Et3P or EtNC, is described. Protonation of these complexes gives the corresponding aryldiimide complexes trans-[Pt(NHNAr)(PEt3)2L]+, and reduction of the protonated complexes with molecular hydrogen in the presence of a catalyst gives the arylhydrazine complexes trans-[Pt(NH2NHAr)(PEt3)2L]+. Some of the spectroscopic properties of these new complexes are reported and discussed. 相似文献
76.
An alternative to traditional hydrocarbon bioremediation is to pump air through unsaturated soils to create aerobic conditions
and induce biodegradation. This study examines the effects of moisture and nutrient augmentation on biodegradation of petroleum
hydrocarbons in aerated soils. Findings indicate that forced aeration, coupled with additions of nutrients and moisture, stimulate
hydrocarbon-degrading microorganisms and present a feasible approach to bioremediation management. 相似文献
77.
78.
Varieties of spiral wave behavior: An experimentalist's approach to the theory of excitable media 总被引:1,自引:0,他引:1
Winfree AT 《Chaos (Woodbury, N.Y.)》1991,1(3):303-334
Spiral waves in diverse excitable media exhibit strikingly variegated behavior. Mechanistic interpretations of excitability in laboratory systems are commonly tested by comparing the wavelength, period, and meander patterns of the model's spiral waves with laboratory observations, but models seem seldom to be rejected by such tests. The reason may be that almost any excitable medium behaves in many respects like almost any other, if its parameters are properly adjusted within a reasonable range. What generalizations can be made about "excitable media" in the absence of more specifications? It would be useful to distinguish such generic features from idiosyncrasies of specific models. The range of behavioral flexibility of the FitzHugh-Nagumo excitable medium is explored by varying two of its parameters and comparing the results with other excitable media to suggest a generic pattern of parameter dependence. The results exhibit the remarkable diversity of rotor behavior in a single model and provide a database for quantitative testing of mathematical generalizations. 相似文献
79.
80.
Keith C. C. Bancroft Laila H. Morcos Guindi Arthur F. Temple 《Journal of heterocyclic chemistry》1978,15(8):1521-1523
Several 2,1,3-benzothiadiazin-4(3H) one 2,2-dioxides were synthesized as possible sweetening agents by reacting sulfamoyl chloride with various anthranilic acid derivatives. The isolation of 1-methyl-4-methoxy-2,1,3-benzothiadiazine 2,2-dioxide and preparation of 3,4-dihydro-2,1,3-benzothiadiazine 2,2-dioxide is also reported. 相似文献