Structural elucidation of new ferulic acid-containing phenolic dimers and trimers isolated from maize bran

Four new phenolic dimers and trimers that contain ferulic acid moieties were isolated from the alkaline hydrolyzate of insoluble maize bran fiber and their structures were established by 1D/2D NMR and mass spectrometry. The biological role of one dimer remains unclear whereas the dimeric vanillin-ferulic acid-cross-product probably represents an oxidative degradation product from the corresponding diferulate. Both ferulic acid dehydrotrimers are able to cross-link polysaccharide chains. However, the 5-5/8-O-4(H₂O)-triferulic acid may be a cross-link in its identified structure whereas we assume that the identified 8-O-4/8-5(non-cyclic)-triferulic acid arose from a natural 8-O-4/8-5(cyclic)-triferulate analog during the saponification process.     

Measurements of someK-internal conversion coefficients near threshold

TheK-internal conversion coefficients have been measured by the XPG technique for a number of low energyγ-ray transitions whose energies do not exceed theK-binding energies by more than 4 keV. Using Si(Li) detectors in singles and coincidence arrangements, the following results were obtained: 63.1 keV El in¹⁶⁹Tm(α_K=1.02±0.15), 72.0 keV E1 in¹⁸⁷Re (0.75±0.05), 57.8 keV M1 in¹⁶²Ho (11.42±0.67), 56.6 keV M1 in¹⁶⁴Ho (12.04±0.70), and 67.1 keV M1 in¹⁷⁴Lu(10.25±0.58). The experimental results are compared with the theoretical calculations which include transition energies down to 1 keV above threshold.     

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KCd2[N(CN)2]5(H2O)4: an enmeshed honeycomb grid

The title compound, poly[potassium [diaquapenta‐μ₂‐dicyanamido‐dicadmium(II)] dihydrate], {K[Cd₂(C₂N₃)₅(H₂O)₂]·2H₂O}_n, contains two‐dimensional anionic sheets of {[Cd₂{N(CN)₂}(H₂O)₂]⁻}_n with a modified (6,3)‐net (layer group , No. 35). Two sets of equivalent sheets interpenetrate orthogonally to form a tetragonal enmeshed grid.     

Coulomb excitation studies of 160Dy, 162Dy and 164Dy

Coulomb excitation measurements with ¹⁶O and ⁴He projectiles have been performed on ¹⁶⁰Dy, ¹⁶²Dy, and ¹⁶⁴Dy. The ground-state rotational bands up through the 8⁺ member were observed in the ¹⁶O experiments. The measured excitation probabilities yield B(E2; I → I ?2) values which are generally in agreement with the rotational predictions except for the 6⁺ → 4⁺ values. In each nucleus, probabilities for exciting the 2⁺, 4⁺, and 6⁺ members of the γ-vibrational band were measured and compared with calculated results. The B (E2; 0⁺ → 2⁺γ) values were measured in experiments involving ⁴He ions. The K^π = 2^? octupole band was observed in each nucleus in addition to 1^? bands in ¹⁶⁰Dy and ¹⁶²Dy. Excitation probabilities were analyzed in an attempt to extract B(E3) values.     

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Total syntheses of (+/-)-beta-erythroidine and (+/-)-8-oxo-beta-erythroidine by an intramolecular Diels-Alder cycloaddition of a 2-amidoacrolein

[reaction: see text] The total syntheses of (+/-)-beta-erythroidine and (+/-)-8-oxo-beta-erythroidine are described. The tetracyclic ring system of the natural products was quickly assembled by a strategy that features a retrocycloaddition/cycloaddition reaction of an amidodioxin, an intramolecular Heck reaction, and a 6pi-electrocyclic ring closure of a dienoic acid.