Electronic absorption and fluorescence study of ionization and intramolecular hydrogen-bonding in the α, β-o-hydroxynaphthoic acids
✍ Scribed by Stephen G. Schulman; Peter J. Kovi
- Book ID
- 108304859
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 876 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0003-2670
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The strength of the intramolecular hydrogen bonds of the methyl mono-and di-0-methyl-#Lo-xylopyranosides, methyl mono-and di-O-benzyl-/3-o-xylopyranosides, benzyl di-0-benzyl-/3-o-xylopyranosides, and mono-and di-Oacetyl-J?-o-xylopyranosides was measured in terms of the frequency of the hydroxyl str
Various derivatization methods have been tested for their usefulness in determining the position of double bonds in a,band b,g-unsaturated isoprenoid acids by gas chromatography/electron ionization mass spectrometry. Stereospecific oxidation with osmium tetroxide followed by trimethylsilylation gave