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Citation
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HERO ID
8309871
Reference Type
Journal Article
Title
Catalyst-controlled site-selective N-H and C3-arylation of carbazole via carbene transfer reactions
Author(s)
Bera, SS; Bahukhandi, SB; Empel, C; Koenigs, RM; ,
Year
2021
Is Peer Reviewed?
Yes
Journal
Chemical Communications
ISSN:
1359-7345
EISSN:
1364-548X
Publisher
ROYAL SOC CHEMISTRY
Location
CAMBRIDGE
Page Numbers
6193-6196
Language
English
PMID
34048520
DOI
10.1039/d1cc01863a
Web of Science Id
WOS:000655732400001
URL
http://xlink.rsc.org/?DOI=D1CC01863A
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Abstract
A site-selective direct arylation reaction of carbazole and other N-heterocycles with diazo-naphthalen-2(1H)-ones has been developed. While Au(i)-NHC catalysts lead to selective C3-arylation, palladium acetate allows for selective N-H arylation, displaying complete site-selectivity each. To show the applicability of these arylation reactions, one-pot, two-fold diarylation reactions of carbazole were demonstrated.
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