Electron impact ionization mass spectrometry and intramolecular cyclization in 2-substituted pyrimidin-4(3H)-ones
Author:
Affiliation:
1. Department of Chemistry, University of Turku, Fin-20500, Turku, Finland
2. Department of Chemistry, University of Tartu, Tartu, Estonia
Publisher
American Chemical Society (ACS)
Subject
Spectroscopy,Structural Biology
Link
https://pubs.acs.org/doi/pdf/10.1016/1044-0305%2894%2985043-7
Reference22 articles.
1. Stereochemical studies. Part 103. Saturated heterocycles part 107. Preparation of 3-mono- and 2,3-di-substituted pyrimidin-4(3H)-ones in retro- Diels–Alder reactions. The correct 1,2-disubstituted structure of the compounds previously described as 2,3-disubstituted derivatives
2. Tautomerism and electron impact mass spectra of pyrimidin-4(3H)- and -4(1H)-ones
3. Sandler, S. R.; Karo, W. Organic Functional Group Preparations1972New York, LondonAcademic Press217217
4. Stájer, G.; Szabó, A. E.; Bernáth, G.; Sohár, P. Synthesis1987, 290.
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