Synthesis of some novel hydrazono acyclic nucleoside analogues

• Mohammad N. Soltani Rad,
• Ali Khalafi-Nezhad and
• Somayeh Behrouz

Beilstein J. Org. Chem. 2010, 6, No. 49, doi:10.3762/bjoc.6.49

• %). Moreover, N-benzyl adenine derivative 1o was obtained as the N(9)-isomer in 76% yield, while theophylline was mostly alkylated at N(7) to afford 1m (69%). All compounds were fully characterized and their structures confirmed by 1H and 13C NMR, elemental analysis, mass and IR spectroscopy. Although

Synthesis of bis(3-{[2-(allyloxy)ethoxy]methyl}-2,4,6-trimethylbenzoyl)(phenyl)phosphine oxide – a tailor-made photoinitiator for dental adhesives

• Norbert Moszner,
• Iris Lamparth,
• Jörg Angermann,
• Urs Karl Fischer,
• Frank Zeuner,
• Thorsten Bock,
• Robert Liska and
• Volker Rheinberger

Beilstein J. Org. Chem. 2010, 6, No. 26, doi:10.3762/bjoc.6.26

• )ethoxy]methyl}-2,4,6-trimethylbenzoyl)(phenyl)phosphine, which was oxidized to WBAPO. The structure of WBAPO was confirmed by 1H NMR, 13C NMR, 31P NMR, and IR spectroscopy, as well as elemental analysis. WBAPO, a yellow liquid, possesses improved solubility in polar solvents and shows UV–vis absorption

• chromatography, WBAPO was obtained as a yellow oil in 67% yield with a HPLC purity of 94–95%. The characterization of WBAPO was carried out by 1H NMR, 13C NMR, 31P NMR and IR spectroscopy, as well as by elemental analysis. The spectral data are in agreement with the expected structure. For example, the presence

A short synthesis of (±)-cherylline dimethyl ether

• Bhima Y. Kale,
• Ananta D. Shinde,
• Swapnil S. Sonar,
• Bapurao B. Shingate,
• Sanjeev Kumar,
• Samir Ghosh,
• Soodamani Venugopal and
• Murlidhar S. Shingare

Beilstein J. Org. Chem. 2009, 5, No. 80, doi:10.3762/bjoc.5.80

• group was confirmed by its IR spectroscopy in which the peak at 1715 cm−1 was observed. Radical azidonation of aldehyde 7 with iodine azide generated in situ by the reaction of sodium azide with ICl) at room temperature gave an acyl azide and subsequent Curtius rearrangement provided isocyanate 10 in

1-(4-Alkyloxybenzyl)-3-methyl-1H-imidazol-3-ium organic backbone: A versatile smectogenic moiety

• William Dobbs,
• Laurent Douce and
• Benoît Heinrich

Beilstein J. Org. Chem. 2009, 5, No. 62, doi:10.3762/bjoc.5.62

• (n > 10) according to the chain length. All imidazolium compounds (18–68, 110–610, 112–612, 114–614, 116–616) were purified by flash chromatography or crystallization. Their structural characterizations and their purities were established by 1H NMR, 13C NMR{1H}, FT-IR spectroscopy and elemental