Copper-Catalyzed\nDearomative [3 + 2] Annulation of\nIndoles with 2‑Iodoacetic Acid

An efficient copper-catalyzed dearomative [3 + 2] annulation\nof\nindoles with 2-iodoacetic acid is developed. By employing Cu(OTf)<sub>2</sub>/2,2′-bis(2-oxazoline) as the catalyst and LPO as the\noxidant, a series of indoline-fused butyrolactones were synthesized\nin moderate to good yields. The reaction features mild conditions,\na broad substrate scope, and readily available starting materials.\nFurthermore, synthetic transformations of the products were conducted\nto demonstrate the practical utility of this reaction.

Publication Details

Journal
Figshare
Published
2024-11-04
DOI
https://doi.org/10.1021/acs.orglett.4c03213.s001
Primary Topic
Ego Development and Educational Practices
Type
article
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article

Copper-Catalyzed\nDearomative [3 + 2] Annulation of\nIndoles with 2‑Iodoacetic Acid

Figshare
Ego Development and Educational Practices
article

Copper-Catalyzed\nDearomative [3 + 2] Annulation of\nIndoles with 2‑Iodoacetic Acid

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Abstract

An efficient copper-catalyzed dearomative [3 + 2] annulation\nof\nindoles with 2-iodoacetic acid is developed. By employing Cu(OTf)<sub>2</sub>/2,2′-bis(2-oxazoline) as the catalyst and LPO as the\noxidant, a series of indoline-fused butyrolactones were synthesized\nin moderate to good yields. The reaction features mild conditions,\na broad substrate scope, and readily available starting materials.\nFurthermore, synthetic transformations of the products were conducted\nto demonstrate the practical utility of this reaction.

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Openalex Percentile: Top 46%
Ego Development and Educational Practices
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Copper-Catalyzed\nDearomative [3 + 2] Annulation of\nIndoles with 2‑Iodoacetic Acid · Figshare (2024) | TGRS Research Map | TGRS