Isolation and structures of euonymine and neoeuonymine,alkaloids from Euonymus Sieboldiana blume

Two new alkaloids, euonymine 5 and neoeuonymine 14 were isolated from Euonymus Sieboldiana Blume. The structures of euonymine and neoeuonymine were established to be 5 and 14, respectively, by chemical and spectral means: the structural features of euonymine 5 are that it is a polyhydroxyl sesquiterpene of eudesman type (euonyminol) which is esterified with evoninic acid 3 and six moles of acetic acid. Neoeuonymine 14 was converted to euonymine 5. Direct conversion of evonine 1 to euonymine 5 was also achieved.     

Raman spectroscopic study of hydrophobic hydration of organic molecules in aqueous solution

Raman spectra of several organic molecules which form hydrate clathrates have been measured in aqueous solution, and the hydration structure around those molecules has been investigated from the analysis of Raman linewidth data.     

A stereochemical investigation of 2-methyl- and 2,5-dimethyl-3-phenyl-1,3-oxazolidines using NMR

The stereochemical properties of two 2-methyl-3-phenyl-1,3-oxazolidines and two of its 5-methyl substituted and four of its 2,5-dimethyl substituted derivatives have been investigated by pmr and cmr methods. The compounds of 2,5-dimethyl-3-phenyl-1,3-oxazolidines exist in isomeric cis and trans forms at the two methyl groups on the heterocyclic ring.     

The stereochemistry of 4-methyl-6-phenyl-5,6,7,8-tetrahydro-4H-1,3,2,6-dioxathiazocine 2-oxides using NMR

Two isomeric 4-methyl-6-phenyl-5,6,7,8-tetrahydro-4H-1,3,2,6-dioxathiazocine 2-oxides were prepared, and their pmr and cmr spectra were examined. From the aromatic solvent shielding values and the magnitudes of the γ shifts, the title compounds are found to exist in the trans and cis forms in solution.     

Copper(II) chloride as a new,efficient additive suppressing racemization in peptide synthesis by the carbodiimide method

Copper(II) chloride was found to be an extremely efficient additive suppressing racemization in the carbodiimide mediated couplings.     

Extraction—spectrophotometric determination of cadmium with diphenylcarbazone in the presence of 1,10-phenanthroline

The addition of 1,10-phenanthroline improves both the extraction and the spectrophotometric sensitivity of the determination of cadmium with diphenylcarbazone. Slope analysis suggests the formation of a 1:2:2 extracted species. The molar absorptivity is 9.4 × 10⁴ l cm^-1 mol^-1 at 536 nm and extraction is maximal at pH 8.2–9.8. Extraction is rapid and absorbances remain constant at room temperature for 48 h. Various divalent metal ions interfere.     

Mass spectral fragmentations of 6-aryl-5,6,7,8-tetrahydro-4H-1,3,2,6-dioxathiazocine 2-Oxides

The mass spectral fragmentation of 4-, 5-, and 4,8-disubstituted derivatives of 6-aryl-5,6,7,8-tetrahydro-4H-1,3,2,6-dioxathiazocine 2-oxides is reported.     

Controlled synthesis of glycopolymers with pendant D-glucosamine residues by living cationic polymerization

D -glucosamine-containing glycopolymers with well-controlled structure were synthesized by living cationic polymerization. To this end, D -glucosamine-containing vinyl ether (VE) of the type [CH₂()CH(OCH₂CH₂OR)] was prepared, where R denotes a 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimide-β-D -glucopyranoside, i.e., the hydroxyl and amino groups in D -glucosamine residues are protected by acetyl and phthaloyl groups, respectively. It was found that (1) the efficient living cationic polymerization of VE monomer is achieved by a combination of ethylaluminum dichloride (EtAlCl₂) with an adduct of trifluoroacetic acid (TFA) and isobutyl VE (IBVE) [CH₃CH(OiBu)OCOCF₃] (i.e., TFA/EtAlCl₂ initiating system); and (2) the polymerization in toluene at the elevated temperature (0°C) is most suitable to proceed the homogeneous polymerization over the whole conversion range. The molecular weight distribution of the resulting polymers was very narrow ($ {\bar M}_w/{\bar M}_n \sim 1.1 $). Quantitative deprotection of the resulting precursor polymers was successfully achieved with hydrazine monohydrate to afford the corresponding water-soluble polymers with pendant D -glucosamine residues. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 751–757, 1997