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. Issue 48 (10th November 2016)

Record Type:: Journal Article
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. Issue 48 (10th November 2016)
Main 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.
Authors:: Deb, Mohit L.
Pegu, Choitanya Dev
Deka, Bhaskar
Dutta, Prantu
Kotmale, Amol S.
Baruah, Pranjal K.
Abstract:: Abstract: 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).
Is Part Of:: ChemInform. Volume 47:Issue 48(2016)
Journal:: ChemInform
Issue:: Volume 47:Issue 48(2016)
Issue Display:: Volume 47, Issue 48 (2016)
Year:: 2016
Volume:: 47
Issue:: 48
Issue Sort Value:: 2016-0047-0048-0000
Page Start:: no
Page End:: no
Publication Date:: 2016-11-10
Subjects:: pyran derivatives -- ring closure reactions, annulation reactions
Chemistry -- Abstracts -- Periodicals
540.5
Journal URLs:: http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1002/chin.201648155 ↗
Languages:: English
ISSNs:: 0931-7597
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 1818.xml