The electronic absorption spectra of n-diazirine, N115-diazirine, d1-diazirine, and d2-diazirine
β Scribed by Lawrence C. Robertson; James A. Merritt
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- English
- Weight
- 719 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0022-2852
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Time-of-Γight secondary ion mass spectrometry (ToF-SIMS) and x-ray photoelectron spectroscopy (XPS) are used to characterize a newly synthesized glycosylated photoactivatable reagent designed for surface glycoengineering. The glycoaryldiazirine reagent diazirine-3-yl)phenyl ] -4-(-3-thio(-1-Dgalacto
## ABSTRACI Three diazirines 2-axi-2-deoxy-o-urabino-hexitol (41, its l-deoxy analogue (S), and 3-axi-3,6-dideoxy-r\_-xylo-hexitol (9) were synthesised and their products of photolysis analysed by TLC. Diazirine 4 gave exclusively 2deoxy-o-arubirw-hexose (121, 5 gave predominantly 1,2-dideoxy-D-er