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Mass spectrometeric study of thiocarbamoyl-substituted 2-aminothiazoles and 2-iminothiazolines. 2. N-thiazolyl- and N-thiazolinylidene-N′-peracetyl glycosylthioureas

✍ Scribed by Ya. V. Rashkes; Yu. M. Mil'grom; R. F. Ambartsumova


Publisher
Springer US
Year
1989
Tongue
English
Weight
348 KB
Volume
25
Category
Article
ISSN
0009-3122

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Mass spectrometric study of thiocarbamoy
✍ Ya. V. Rashkes; Yu. M. Mil'grom; R. F. Ambartsumova 📂 Article 📅 1989 🏛 Springer US 🌐 English ⚖ 492 KB

s, 5-H). Mass spectrum, m/z: 167 (M +, 21), 132 (M + -CI, i00), 105 (46), 79 (ii), 69 (14). Compound VIII, PMR spectrum: 4.58 ppm (s, CH2CI). Mass spectrum, m/z: 201 (M +, 20), 170 (15), 166 (M + -CI i00), 105 (50), 79 (16), 69 (14). Compound VI, PMR spectrum: 2.22 ppm (s, CH3); mass spectrum, m/z:

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Positive-ion liquid secondary ionization mass spectrometry in combination with 3-nitrobenzyl alcohol as the liquid matrix was used to investigate the mass spectral features of a set of 21 N10-substituted derivatives of 2-chlorophenoxazine. The N-10 substitution included propyl, butyl and acetyl grou