Carbene induced rearrangement products from two furoquinolinone scaffolds
Author(s)
Lindahl, Karl-Fredrik
Carroll, Anthony
Quinn, Ronald J
Ripper, Justin A
Year published
2010
Metadata
Show full item recordAbstract
Novel double CH-insertion and rearrangement products (5, 6, and 7) were isolated from treatment of 1 or 2 with dimethyl diazomalonate (3) under dirhodiumtetrakis mediated carbenoid chemistry conditions. A new possible reaction pathway is suggested and discussed. Also other diazo compounds were tested.Novel double CH-insertion and rearrangement products (5, 6, and 7) were isolated from treatment of 1 or 2 with dimethyl diazomalonate (3) under dirhodiumtetrakis mediated carbenoid chemistry conditions. A new possible reaction pathway is suggested and discussed. Also other diazo compounds were tested.
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Journal Title
Journal of Heterocyclic Chemistry
Volume
47
Issue
4
Copyright Statement
Self-archiving of the author-manuscript version is not yet supported by this journal. Please refer to the journal link for access to the definitive, published version or contact the author[s] for more information.
Subject
Organic chemistry
Organic chemical synthesis