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Open AccessJournal ArticleDOI

A new approach for the synthesis of bisindoles through AgOTf as catalyst

TLDR
The simplicity and easy operational methodology using a small amount of commercially available AgOTf, one of the lowest catalytic charge used in this process to date, makes this procedure an alternative approach for this interesting and appealing reaction.
Abstract
A novel approach for the catalyzed formation of bisindolylmethane derivatives (BIMs) is described. This methodology is the unique example where AgOTf has been successfully used for the activation of aldehydes, giving easy access to a broad range of bisindolyl derivatives with excellent results. Moreover, the simplicity and easy operational methodology using a small amount of commercially available AgOTf (1–3 mol %), one of the lowest catalytic charge used in this process to date, makes this procedure an alternative approach for this interesting and appealing reaction.

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Citations
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Journal ArticleDOI

Transition Metal-Catalyzed CH Activation of Indoles

TL;DR: Recent advances and strategies for transition metal-catalyzed CH activation of indoles and a versatile tool box for the preparation of structurally diverse indoles are discussed.
Journal ArticleDOI

Expedient Access to Unsymmetrical Diarylindolylmethanes through Palladium-Catalyzed Domino Electrophilic Cyclization-Extended Conjugate Addition Approach.

TL;DR: A palladium-catalyzed domino process to access unsymmetrical diarylindolylmethanes has been developed through the annulation of o-alkynylanilines followed by 1,6-conjugate addition with p-quinone methides (p-QMs) under relatively mild conditions.
Journal ArticleDOI

Synthesis of bis(indolyl)methanes using ammonium niobium oxalate (ANO) as an efficient and recyclable catalyst

TL;DR: A green and efficient procedure was developed for the synthesis of bis(indolyl)methanes using ammonium niobium oxalate (ANO) NH4[NbO(C2O4)2(H2O)x]·nH 2O as the catalyst and water or glycerol as the solvent.
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Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel–Crafts alkylation

TL;DR: A series of custom-designed, high yield, isoskeletal tetranuclear Zn/4f coordination clusters showing high efficiency as catalysts with low catalytic loadings in Friedel-Crafts alkylation are described for the first time.
Journal ArticleDOI

The natural and synthetic indole weaponry against bacteria

TL;DR: A brief account of indole based antibacterial small molecules which have been either synthesized in the laboratory or isolated from natural sources and provide intriguing potential leads in the antibiotic drug discovery research are presented.
References
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Journal ArticleDOI

Marine indole alkaloids: potential new drug leads for the control of depression and anxiety

TL;DR: Information is provided on current and potential pharmaceuticals including small molecule natural indole alkaloids to their biological properties, structure-activity relationship studies, and especially their potential for the treatment of neurological disorders, including depression.
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Catalytic Functionalization of Indoles in a New Dimension

TL;DR: This Review emphasizes the achievements in the selective catalytic functionalization of indoles (C-C bond-forming processes) over the last four years.
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Bis- and Trisindolylmethanes (BIMs and TIMs)†

TL;DR: The main purpose of this review is to provide a comprehensive summary of the various synthetic strategies to synthesize BIMs and TIMs.
Journal ArticleDOI

Structure, Bioactivity and Synthesis of Natural Products with Hexahydropyrrolo[2,3‐b]indole

TL;DR: This review summarizes the structures, biological activities, and synthetic routes for natural compounds containing HPI, emphasizing the different strategies for assembling this motif.
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