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11.
12.
Dieter Wolke 《Monatshefte für Mathematik》1990,110(1):73-78
It is shown by analytical means that, if one assumes the Riemann hypothesis, the asymptotic formula $$\sum\limits_{n \leqslant x} {\omega (n) = x 1n1n } x + B - x\int_l^{x^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2}} } {\frac{{\{ t\} }}{{t^2 (1n x - 1n t)}}dt + O(x^{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-\nulldelimiterspace} 2} + \varepsilon } )} $$ holds. This improves a result ofB. Saffari, who got a weaker error term by using the Dirichlet “hyperbola method”. The above formula, in turn, implies the Riemann hypothesis. 相似文献
13.
γ-Lactone-cis-annulation to Δ2- and Δ3- Cholestene. From Δ2- and Δ3- cholestene the γ-lactones 11a , 11b , 12a , and 12b are synthesized through the dibromocarbene adducts 3 and 4 , the bromohydrines 5 and 6 , the oxapiropentanes 7 and 8 , and the cyclobutanones 9a , 9b and 10a , 10b , respectively. The 13C-NMR.-spectra of 1–8 and 11 as well as the ORD.-spectra of the cyclobutanones 9 and 10 are reported. 相似文献
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η5-C5H5V(NO)2CO is prepared in 40% yield by the photo-reaction between η5-C5H5V(CO)4 and [Co(NO)2Br]2.η5-C5H5V(NO)2CO reacts by an SN1 mechanism with various phosphines PZ3 to yield η5-C5-H5V(NO)2PZ3. The phosphine complexes are also obtained by photo-induced ligand interchange between η5-C5H5V(CO)3PZ3 and [Co(NO)2Br]2, or η5-C5H5V(CO)4 and Co(NO)2Br(PZ3). In all cases, the main cobalt species formed is Co(NO)(CO)3. While the one-bond vanadiumphosphorus coupling constants of most of the phosphine complexes are virtually the same (ca 410 Hz),the chemical shift values δ(51V) (?1328 to ?973 ppm rel. VOCl3) decrease in the order PF3 > CO > P(OR)3 > P(alkyl)3 > PPh3 > PPh(NEt2)2, reflecting the decreasing π-acceptor ability of the ligands. δ(51V) also decreases in the series of alkylphosphines PR3 (R = Me, Et, Prn, Bui, Pri, BUt) as the cone angle of PR3increases. 相似文献
17.
Perfluoroalkyl iodine compounds: preparations and properties of CF3IO, CF3IOF2, and CF3IO2. The trifluoromethyl iodine compounds CF3IO, CF3IOF2, and CF3IO2 are formed from the reactions of CF3I, CF3IF2 or CF3IF4 with ozone or silicon dioxide respectively. Their preparartions, properties, 19F-nmr spectra, and ir spectra are described. 相似文献
18.
On Ternary Chalcogenides. XXIV. The Structure of TlGaSe2 TlGaSe2 is monoclinic with a = 10.772(3), b = 10.771(5), c = 15.636(8) Å, ß = 100.6(3)°, Z = 16, space group Cc. The refinement yielded an R value of 0.082 for 1366 unique observed reflections (MoKα). The compound crystallizes with a layer structure with two anion layers perpendicular to c* in the unit cell. The structural motive of the layers are large corner-linked Ga4Se10- tetraeder consisting of four corner-linked GaSe4 tetrahedra. Two adjacent layers are turned relative to each other by 90°. They are kept together by Tl1+ ions, which are situated on straight lines parallel to the edges of the Ga4Se10 groups. They are surrounded by six selenium atoms forming trigonal-prismatic TlSe6 polyhedra. 42 screw-axes within the layers are the reason for a strongly pronounced pseudo tetragonal symmetry. Different possibilities of stacking cause a onedimensional disorder along the c* direction. The relations between the TlGaSe2 type and the TlSe type and also the high-pressure modifications of some compounds with the TlGaSe2 structure are discussed. 相似文献
19.
Enantioselective Synthesis of Allyl-, Propargyl-, and 4-En-2-ynyl-amines via 1,2-Addition of Organocerium Reagents to Chiral Aldehyde Imines (E)- and (Z)-Allyl-, propargyl-, and 4-en-2-ynyl-amines 5 and 14 , useful bifunctional building blocks and of pharmaceutical interest, are synthesized in high enantiomeric purity (e.e. ≥ 97%). Key step is the diastereoselective 1,2-addition (d.e. 86 to ≥ 98%) of organocerium reagents to chiral α,β-unsaturated aldehyde imines 3 or 8 to produce adduct amines 4 and 9 (Schemes 1 and 4, resp.). The propargylamine 9 is a substrate for Pd-catalyzed coupling with alkenyl halides to produce the enynylamine 11a and the thienyl-substituted alkynylamine 11b . The chiral auxiliary (S,S)- 2 is removed from 4 and 11 in 3 steps affording the title compounds 5 and 14 . Diastereoisomer enrichment of the hydrochloride of 6 by crystallization is possible. 相似文献
20.
The phenolic oxidation of 2',4-dihydroxy-4'-methoxy-β-methylchalcone using alkaline potassium ferricyanide gives an aurone rather than an isoflavone. This result is discussed in the context of current theories regarding the biosynthesis of flavonoid and isoflavonoid compounds. 相似文献