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.
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pyran derivatives
ring closure reactions, annulation reactions
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container_issue 48
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container_title ChemInform
container_volume 47
creator Deb, Mohit L.
Pegu, Choitanya Dev
Deka, Bhaskar
Dutta, Prantu
Kotmale, Amol S.
Baruah, Pranjal K.
description 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).
doi_str_mv 10.1002/chin.201648155
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subjects pyran derivatives
ring closure reactions, annulation reactions
title 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
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