Stereospecific fragmentation processes in cycloalkane/cycloalkene-fused isomers of saturated pyrrolo[2,1-b][1,3]oxazin-6-one derivatives
Author:
Affiliation:
1. Department of Chemistry, University of Turku, FIN-20014, Turku, Finland
2. Institute of Pharmaceutical Chemistry, Albert Szent-Györgyi Medical University, Szeged, Hungary
Publisher
American Chemical Society (ACS)
Subject
Spectroscopy,Structural Biology
Link
https://pubs.acs.org/doi/pdf/10.1016/S1044-0305%2899%2900011-2
Reference7 articles.
1. Stereochemical Effects in the Electron Ionization Mass Spectra of Cycloalkane-(alkene)-fused 2,3-Dihydro-5H-thiazolo[3,2-a]pyrimidine-5-ones and 3,4-Dihydro-2H,6H-pyrimido[2,1-b]thiazin-6-ones
2. Stereochemical Effects in the Mass Spectra ofcis-andtrans-2-Aryl-4a,5,6,7,8,8a-hexahydroquinazolin-4(3H)-ones
3. Structures of pyrrolo-1,3-heterocycles prepared from 3-aroylpropionic acid and cyclic aminoalcohols: an NMR and X-ray diffraction study
4. Non-stereospecific hydrogen migrations accompanying Retro-Diels-Alder fragmentations in some adducts of cyclopentadiene and 1,3-cyclohexadiene under electron impact
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