Formation of new 5,11b-bridged isoindolo
Identifieur interne : 001050 ( France/Analysis ); précédent : 001049; suivant : 001051Formation of new 5,11b-bridged isoindolo
Auteurs : Hucher [France] ; Dalch ; DecroixSource :
- Organic letters [ 1523-7052 ] ; 2000.
Abstract
[formula: see text] The tandem Pummerer/pi-aromatic cyclization of alpha-acyliminium ion, leading efficiently in "one pot" to thiopoxyareno-bridged isoindoloisoquinolinone incorporating the arylthio group, has been demonstrated for the first time. During this sequence the angular hydroxylated isoindoloisoquinolinone, resulting from the Pummerer-type cyclization, was also obtained.
PubMed: 10810707
Affiliations:
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- to stream Main, to step Exploration: 001849
- to stream France, to step Extraction: 001050
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pubmed:10810707Le document en format XML
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