Transamination of\nZwitterionic\nQuinones with Polyamines:\nThe Carbon Bridge Matters

The\none-pot transamination reactions on a zwitterionic benzoquinonemonoimine\nyield either a quinoxaline derivative or bis-zwitterionic macrocycles,\ndepending on the number of carbon atoms bridging primary polyamines.\nThese latter products, featuring two confined donor cavities, are\nthe result of a [2 + 2] condensation without the need for template\neffect or high dilution conditions.

Publication Details

Journal
Figshare
Published
2024-12-31
DOI
https://doi.org/10.1021/acs.joc.4c02100.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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Transamination of\nZwitterionic\nQuinones with Polyamines:\nThe Carbon Bridge Matters

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Mycorrhizal Fungi and Plant Interactions
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Transamination of\nZwitterionic\nQuinones with Polyamines:\nThe Carbon Bridge Matters

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Abstract

The\none-pot transamination reactions on a zwitterionic benzoquinonemonoimine\nyield either a quinoxaline derivative or bis-zwitterionic macrocycles,\ndepending on the number of carbon atoms bridging primary polyamines.\nThese latter products, featuring two confined donor cavities, are\nthe result of a [2 + 2] condensation without the need for template\neffect or high dilution conditions.

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Mycorrhizal Fungi and Plant Interactions
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Transamination of\nZwitterionic\nQuinones with Polyamines:\nThe Carbon Bridge Matters · Figshare (2024) | TGRS Research Map | TGRS