ChemInform Abstract: Broensted‐Acid‐Mediated Divergent Reactions of Betti Bases with Indoles: An Approach to Chromeno[2,3‐b]indoles Through Intramolecular Dehydrogenative C2‐Alkoxylation of Indole

ChemInform Abstract: Broensted‐Acid‐Mediated Divergent Reactions of Betti Bases with Indoles: An Approach to Chromeno[2,3‐b]indoles Through Intramolecular Dehydrogenative C2‐Alkoxylation of Indole

Under Broensted acid catalysis, naphthol‐based Betti bases either couple with indoles or undergo a new type of C—C bond cleavage giving diarylmethanes (not shown).

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Veröffentlicht in:ChemInform 2016-11, Vol.47 (48), p.no-no
Hauptverfasser: Deb, Mohit L., Pegu, Choitanya Dev, Deka, Bhaskar, Dutta, Prantu, Kotmale, Amol S., Baruah, Pranjal K.
Format: Artikel
Sprache:eng
Schlagworte:
pyran derivatives
ring closure reactions, annulation reactions
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Zusammenfassung:Under Broensted acid catalysis, naphthol‐based Betti bases either couple with indoles or undergo a new type of C—C bond cleavage giving diarylmethanes (not shown).
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201648155