2021
DOI: 10.6023/cjoc202007055
|View full text |Cite
|
Sign up to set email alerts
|

Access to Tetrasubstituted Tri(indolyl)methanes through Copper-Catalyzed Addition/Substitution Sequence

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2023
2023

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 8 publications
0
1
0
Order By: Relevance
“…Electrophilic substitution occurs readily on indole due to excessive π-electron delocalization. 8 Indole is reactive at four different positions including carbon atom 3, 9–13 nitrogen atom 1, the C2–C3 π-bond 14–17 and the C2–N sigma bond 18,19 (Fig. 2).…”
Section: Introductionmentioning
confidence: 99%
“…Electrophilic substitution occurs readily on indole due to excessive π-electron delocalization. 8 Indole is reactive at four different positions including carbon atom 3, 9–13 nitrogen atom 1, the C2–C3 π-bond 14–17 and the C2–N sigma bond 18,19 (Fig. 2).…”
Section: Introductionmentioning
confidence: 99%