2022
DOI: 10.1039/d1ra09233b
|View full text |Cite
|
Sign up to set email alerts
|

Recent advances in the synthesis of thienoindole analogs and their diverse applications

Abstract: Synthesis of thienoindoles via easy and atom economical approaches followed by their potent applications.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 74 publications
0
2
0
Order By: Relevance
“…112 Their efficacy lies in their ability to yield the desired products in one pot and one step, making them an easy and atom economical approach. 113 MCRs involve more than two reactants, which selectively react with each other to give the desired product. Various bioactive heterocyclic compounds and drug molecules have been developed using these environmentally benevolent reactions.…”
Section: Dalton Transactions Perspectivementioning
confidence: 99%
“…112 Their efficacy lies in their ability to yield the desired products in one pot and one step, making them an easy and atom economical approach. 113 MCRs involve more than two reactants, which selectively react with each other to give the desired product. Various bioactive heterocyclic compounds and drug molecules have been developed using these environmentally benevolent reactions.…”
Section: Dalton Transactions Perspectivementioning
confidence: 99%
“…In support of this, thienoindole ring systems, sulfur-containing analogs of selenophenoindoles, were widely used as the basis of biologically active compounds 15 and organic semiconductors. 16 However, in contrast to thienoindoles, the methods for the synthesis of selenophenoindoles are very limited in the literature. Thus, two approaches were recently suggested for the synthesis of selenopheno[2,3- b ]indoles, including the electrophilic cyclization of 3-(arylethynyl)indoles 1 with in situ generated SeCl 2 to form 2-aryl-substituted derivatives 2 17 (Scheme 1a) and IBr-promoted three-component reaction of indoles 3 with acetophenones or some hetaryl methyl ketones and selenium powder to form 3-(hetero)aryl-substituted derivatives 4 (Scheme 1b).…”
Section: Introductionmentioning
confidence: 99%