Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2024 Aug 13;9(34):36023-36042.
doi: 10.1021/acsomega.4c02848. eCollection 2024 Aug 27.

Visible-Light-Induced Dearomative Annulation of Indoles toward Stereoselective Formation of Fused- and Spiro Indolines

Affiliations
Review

Visible-Light-Induced Dearomative Annulation of Indoles toward Stereoselective Formation of Fused- and Spiro Indolines

Suven Das. ACS Omega. .

Abstract

Dearomatization approaches are attractive for their abilities to transform simple, planar arenes into complex, three-dimensional architectures. In particular, visible-light driven dearomatization strategies are significant because of their mild, green, and sustainable nature, enabling the fabrication of new chemical bonds via an electron transfer or energy transfer process. Indole compounds, being potentially bioactive and readily accessible, can be employed efficiently as building blocks for constructing diverse annulated frameworks under photocatalysis. Highly stereoselective radical cascade reactions of appropriate indole systems can provide complex cyclic scaffolds bearing multiple stereocenters. In fact, the past few years have witnessed the renaissance of dearomative cycloadditions of indoles via visible-light-induced photocatalysis. The present review highlights recent advances (2019-mid 2024) in visible-light-driven dearomative annulation of indoles leading to formation of polycyclic indolines, including angularly fused and spiro indolines. Most of the reactions described in this review are simple, providing quick access to the desired products. Additionally, characteristic reaction mechanisms are offered to provide an understand of how indole scaffolds show distinctive reactivity under photocatalytic conditions.

PubMed Disclaimer

Conflict of interest statement

The author declares no competing financial interest.

Figures

Figure 1
Figure 1
Representative examples of natural products containing an indoline skeleton.
Figure 2
Figure 2
Visible-light-induced formation of fused, angularly fused, and spiro-indolines from indole derivatives.
Scheme 1
Scheme 1. Visible-Light-Driven Reaction between Tryptamines and Alkynyl Sulfones to Afford Pyrroloindoline Scaffolds in the Presence of Ir-Photocatalyst
Scheme 2
Scheme 2. Light-Induced Assembly of Electron-Deficient Indoles and Glycines toward Lactam-Fused Indolines in the Presence of an Organic Photocatalyst
Scheme 3
Scheme 3. Visible-Light Photocatalyzed Intermolecular Α-Aminomethyl/Carboxylative Dearomatization of Indoles with CO2 and Radical Precursors
Scheme 4
Scheme 4. Photocatalytic Synthesis of Prenylated Indolines from α-Silylamines and Indoles
Scheme 5
Scheme 5. Rapid Access to Pyrroloindolines from N-Propargylindoles and Acyl Chlorides under Photocatalysis
Scheme 6
Scheme 6. Tunable Photocatalytic C-H Functionalization and Dearomative Annulation Involving Indole-Tethered Ketones
Scheme 7
Scheme 7. Visible-Light-Promoted Palladium-Catalysis of N-(2-Bromobenzoyl)indoles and Alkenes to Access Fused Indolines
Scheme 8
Scheme 8. Photocatalytic Dearomative Arylcarboxylation of Indoles for Accessing Indoline-3-Carboxylic Acid Derivatives
Scheme 9
Scheme 9. Direct Photoinduced Reductive Heck Cyclization of Indoles to Obtain Indolino-Isoindolones
Scheme 10
Scheme 10. Dearomative Photoredox Radical–Polar Crossover Reaction of Pyridine-Tethered Indoles toward Fused Indoline Motifs
Scheme 11
Scheme 11. Visible-Light-Assisted Dearomatization of N-(o-Haloarylformyl)indoles in an EDA Complex of Thiophenol for Accessing Indoline Derivatives
Scheme 12
Scheme 12. Metallophotoredox Dearomatization of Indoles for Facile Entry to Indolo[2,3-c]isoquinolin-5-ones
Scheme 13
Scheme 13. Intermolecular Aza-Paternò–Büchi Reaction of Indoles and N-Sulfonylimines Leading to Azetidine-Fused Pentacyclic Indolines
Scheme 14
Scheme 14. Photocatalyst-Free Paternò–Büchi Reaction of Indoles and Aromatic Ketones for Affording Oxeto[2,3-b]indoles
Scheme 15
Scheme 15. Visible-Light Excited Ag3PO4 (NPs) Assisted Synthesis of Benzofuroindolines
Scheme 16
Scheme 16. Photoredox Asymmetric Dearomatization of Indole Derivatives with N-Hydroxycarbamates Promoted by Ir/CPA Dual Catalysis
Scheme 17
Scheme 17. Imidazoacridine-Based Photosensitizer (ACR-IMAC) for [2 + 2] Photocycloaddition of Indoles and Olefins Resulting in Cyclobutane-Fused Indolines
Scheme 18
Scheme 18. [2π + 2σ]-Photocycloaddition Reaction of Indoles with Bicyclo[1,1,0]butanes Affording Bicyclo[2,1,1]hexanes
Scheme 19
Scheme 19. CrIII-Photocatalyzed Dearomative [3 + 2] Cycloaddition between Indoles and Vinyldiazo Compounds to Afford Cyclopentene Fused Indolines
Scheme 20
Scheme 20. Gd(III)-Photocatalysis Enabled a Dearomative [2 + 2] Cycloaddition/Ring Expansion Sequence with Indoles toward Cyclopenta[b]indolines
Scheme 21
Scheme 21. Ir-Photoredox Catalyzed Stereoselective Synthesis of Hexahydrocarbazoles from Tryptophans and Acrylamides
Scheme 22
Scheme 22. Synthesis of Cyclobutane-Fused Indolines via Photocatalytic Divergent Dearomatization of Indoles
Scheme 23
Scheme 23. Visible-Light-Induced Intramolecular Dearomatization of Indole Derivatives to Access Cyclobutane-Fused Angular Tetracyclic Indolines
Scheme 24
Scheme 24. [2 + 2] Photocyclization of 3-(Hexa-4,5-dienyl)indoles Sensitized by 3,4-Dimethoxy Acetophenone to Form Methylenecyclobutane Fused Angular Tetracyclic Indolines
Scheme 25
Scheme 25. Intramolecular [2 + 2] Photocycloaddition of Indole Derivatives toward Indoline Embedded Cyclobutane-Fused Pyrrolidinones Using Ir(dFppy)3 or Organic Photosensitizer
Scheme 26
Scheme 26. Photoredox-Catalyzed [2 + 2] Cycloaddition of Enaminone Tethered Indoles to Furnish Cyclohepta[b]indoles
Scheme 27
Scheme 27. Photocatalytic Cyclization of Indole-Alkyne Compounds with NaHSO3 Leading to Indoline Fused Sulfonyl Polycycles
Scheme 28
Scheme 28. Photochemical Transformation of Allene Tethered Indoles into Tetracyclic Cyclobutane-Fused Indoline Scaffolds Using an Aromatic Ketone Photosensitizer
Scheme 29
Scheme 29. Visible-Light-Promoted Dearomative Cyclization of Olefin-Tethered Indoles Process to Prepare Cyclobutane Fused Polycyclic Indolines
Scheme 30
Scheme 30. Dearomative [2 + 2] Cycloaddition of Indole-Tethered Alkynes with an Ir-Based Photosensitizer for the Synthesis of Cyclobutene-Fused Indolizidines
Scheme 31
Scheme 31. Photocatalytic [2 + 2] Cycloaddition of Aliphatic Amine Bearing Indoles toward Strained Indolines
Scheme 32
Scheme 32. Photocatalytic Dearomative [2 + 2] Cycloaddition of Indole-Tethered O-Methyl Oximes to Achieve Indoline-Fused Azetidines
Scheme 33
Scheme 33. Visible-Light-Mediated [5 + 2]/[2 + 2] Cycloaddition Involving Indole-Tethered VCPs toward Cycloheptane/Cyclobutane-Fused Indolines
Scheme 34
Scheme 34. Visible-Light-Driven Double Dearomative Cycloaddition of Arene-Tethered Indoles for the Construction of Bridged Cyclic Indolines
Scheme 35
Scheme 35. Light-Induced Dearomative Spirocyclization of Indoles toward Spiroazetidine/Spiroindane Indolines
Scheme 36
Scheme 36. Photoredox-Catalyzed Reaction of Indole-Substituted Bromodifluoroacetamide and Phosphine Oxide toward Synthesis of Spiroindolines
Scheme 37
Scheme 37. Light-Promoted Catalyst-Free Dearomative Spirocyclization of Indole-Tethered Ynones and Thiols to Access Sulfur-Containing Spirocyclic Indolines
Scheme 38
Scheme 38. Visible-Light-Mediated Spirocyclization of Indole Ynones with Diselenides to Obtain 3-Selenospiroindolines
Scheme 39
Scheme 39. Photocatalytic Intermolecular Dearomative Cyclization of Indole-Derived Bromides with Alkynes Affording Spiroindolines
Scheme 40
Scheme 40. Visible-Light-Initiated Dearomative Oxamination Reaction of Anilide-Tethered Indoles toward Spiroindolines
Scheme 41
Scheme 41. Red-Light-Induced Cascade Trifluoromethylation and Dearomatization of Indole Derivatives with Umemoto’s Reagent to Access 3,3′-Spirocyclic Indolines
Scheme 42
Scheme 42. Photocatalytic Radical Insertion Reaction of 3-(2-Isocyanobenzyl)-Indoles and Bromodifluoroacetates to Offer Spiro[indole-3,3′-quinoline] Derivatives
Scheme 43
Scheme 43. Visible-Light-Induced Spirocyclization of 3-(2-Isocyanobenzyl)-Indoles with Diselenides, Affording Selenyl Spiro[indole-3,3′-quinoline] Derivatives
Scheme 44
Scheme 44. Synthesis of Spiropiperidino Indolines via Blue LED Driven Cyclopropanation of Tryptamine Derivatives

Similar articles

References

    1. Umer S. M.; Solangi M.; Khan K. M.; Saleem R. S. Z. Indole-Containing Natural Products 2019–2022: Isolations, Reappraisals, Syntheses, and Biological Activities. Molecules 2022, 27, 7586.10.3390/molecules27217586. - DOI - PMC - PubMed
    1. Duan S.-F.; Song L.; Guo H.-Y.; Deng H.; Huang X.; Shen Q.-K.; Quan Z.-S.; Yin X.-M. Research Status of Indole-Modified Natural Products. RSC Med. Chem. 2023, 14, 2535–2563. 10.1039/D3MD00560G. - DOI - PMC - PubMed
    1. Mathada B. S.; Yernale N. G.; Barsha J. N. The Multi-Pharmacological Targeted Role of Indole and its Derivatives: A review. ChemistrySelect 2023, 8, e20220418110.1002/slct.202204181. - DOI
    1. Kaushik N. K.; Kaushik N.; Attri P.; Kumar N.; Kim C. H.; Verma A. K.; Choi E. H. Biomedical Importance of Indoles. Molecules 2013, 18, 6620–6662. 10.3390/molecules18066620. - DOI - PMC - PubMed
    1. Kim T.; Ha M. W.; Kim J. Recent Advances in Divergent Synthetic Strategies for Indole-Based Natural Product Libraries. Molecules 2022, 27, 2171.10.3390/molecules27072171. - DOI - PMC - PubMed

LinkOut - more resources