Stereospecific fragmentations in the mass spectra of stereoisomeric isoindoloquinazolines
Author:
Affiliation:
1. Structural Chemistry Group, Department of Chemistry, University of Turku, FIN-20014, Turku, Finland
2. Institute of Pharmaceutical Chemistry, University of Szeged, Szeged, Hungary
Publisher
American Chemical Society (ACS)
Subject
Spectroscopy,Structural Biology
Link
https://pubs.acs.org/doi/pdf/10.1016/S1044-0305%2803%2900408-2
Reference14 articles.
1. Stájer G.; Szabó A. E.; Sohár P.; Szúnyog J.; Bernáth G. The First Preparation of a Heterotricycle, [1,3]Oxazino[2,3-a]Isoindole-2,6-Dione, by a Retro-Diels-Alder Method. Synthesis1998, 718–720.
2. Synthesis and Structure of Norbornane/ene-fused Thiouracils and Thiazino[3,2-a]pyrimidinones
3. Saturated Heterocycles, Part 257. Preparation and Structure of Partially Saturated Isoindolo[1,2-b]- and -[2,1-a]quinazolinones
4. Mandelbaum, A. Stereochemical Effects in the Retro-Diels-Alder Fragmentation. In Applications of Mass Spectrometry to Organic Stereochemistry; 1994; 299–324.
5. Stereospecific Retro-Diels-Alder fragmentation of stereoisomeric 3-methoxy- and 3,6-dialkoxytricyclo[6.2.2.02,7]dodeca-9-enes upon electron ionization
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1. Electron ionization mass spectra of naphthoxazine, naphthpyrrolo-oxazinone and naphthoxazinobenzoxazine derivatives;Arkivoc;2008-08-17
2. Mass spectra of tetrahydroisoquinoline-fused 1,3,2-O,N,P- and 1,2,3-O,S,N-heterocycles: influence of ring size and fusion, of present heteroatoms, substituent effects and of the stereochemistry on fragmentation;Rapid Communications in Mass Spectrometry;2008
3. Does the electron ionization induced fragmentation of partly saturated stereoisomeric pyrrolo- and isoindoloquinazolinones show stereospecificity?;Rapid Communications in Mass Spectrometry;2007
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