Does the electron ionization induced fragmentation of partly saturated stereoisomeric pyrrolo- and isoindoloquinazolinones show stereospecificity?
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference12 articles.
1. Stereospecific fragmentations in the mass spectra of stereoisomeric isoindoloquinazolines
2. Saturated Heterocycles, Part 257. Preparation and Structure of Partially Saturated Isoindolo[1,2-b]- and -[2,1-a]quinazolinones
3. Preparation and structure of pyrrolo- and isoindoloquinazolinones
4. Selective non-nucleoside HIV-1 reverse transcriptase inhibitors. New 2,3-dihydrothiazolo[2,3-a]isoindol-5(9bH)-ones and related compounds with anti-HIV-1 activity
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1. Pyrroloquinolines, imidazoquinolines, and pyrroloquinazolines with a bridgehead nitrogen;Advances in Heterocyclic Chemistry;2019
2. Pyrrolo[1,2-a]quinazolines: synthesis and biological properties;Arkivoc;2014-07-11
3. A Novel Approach for the Synthesis of N-Arylpyrroles;Synlett;2009-11-18
4. Electron ionization mass spectra of naphthoxazine, naphthpyrrolo-oxazinone and naphthoxazinobenzoxazine derivatives;Arkivoc;2008-08-17
5. Electron ionization mass spectra of aryl- and benzyl-substituted 2,3-dihydroimidazo[1,2-a]pyrimidine-5,7(1H,6H)-diones;Rapid Communications in Mass Spectrometry;2007
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