1998
DOI: 10.1016/s0040-4020(98)00172-0
|View full text |Cite
|
Sign up to set email alerts
|

A new synthesis of 3-aryl substituted oxindoles

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

1998
1998
2015
2015

Publication Types

Select...
3
2
1

Relationship

0
6

Authors

Journals

citations
Cited by 13 publications
(1 citation statement)
references
References 28 publications
0
1
0
Order By: Relevance
“…The most commonly employed methods for the synthesis of this motif are the addition of aryl nucleophiles to isatins (Grignard reagents and boronic acids), inter- and intramolecular Friedel−Crafts hydroxyalkylations, oxidative hydroxylation of 3-aryloxindoles, and S N Ar reactions of 2-fluoronitroarenes on dioxolanone templates . Asymmetric variants of many of these approaches are known. ,,, …”
mentioning
confidence: 99%
“…The most commonly employed methods for the synthesis of this motif are the addition of aryl nucleophiles to isatins (Grignard reagents and boronic acids), inter- and intramolecular Friedel−Crafts hydroxyalkylations, oxidative hydroxylation of 3-aryloxindoles, and S N Ar reactions of 2-fluoronitroarenes on dioxolanone templates . Asymmetric variants of many of these approaches are known. ,,, …”
mentioning
confidence: 99%