Strategies Employing Transition‐Metal Free Conditions for C−C Bond Formation in Indoles

Abstract Indole motifs are omnipresent in nature and can be found in many natural products as well as pharmaceuticals. It is for this reason synthetic transformations of indole have become a topic of interest for the organic and medicinal chemist community for decades. In this review, we have emphasized the functionalization of indoles via transition‐metal‐free approaches. This review touches on many aspects in different sub‐sections, which gives a proposition of the tactics employed for the functionalization of indoles and an overview of the road ahead.

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Journal
ChemistrySelect
Published
2024-09-01
DOI
https://doi.org/10.1002/slct.202403280
Citations
1
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.16
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article

Strategies Employing Transition‐Metal Free Conditions for C−C Bond Formation in Indoles

Balaji M. Ghodake, Sayantan Paul, Asish K. Bhattacharya
1 citations
ChemistrySelect
Asymmetric Hydrogenation and Catalysis
0.16
article

Strategies Employing Transition‐Metal Free Conditions for C−C Bond Formation in Indoles

Balaji M. Ghodake, Sayantan Paul, Asish K. Bhattacharya
article en
1 citations

Abstract

Abstract Indole motifs are omnipresent in nature and can be found in many natural products as well as pharmaceuticals. It is for this reason synthetic transformations of indole have become a topic of interest for the organic and medicinal chemist community for decades. In this review, we have emphasized the functionalization of indoles via transition‐metal‐free approaches. This review touches on many aspects in different sub‐sections, which gives a proposition of the tactics employed for the functionalization of indoles and an overview of the road ahead.

ChemistrySelectVol. 9(36)
National Chemical Laboratory (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 58%
Asymmetric Hydrogenation and Catalysis
0.16
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