Mo-MediatedReductive Cyclization/Allylation of 2‑AlkynylNitroarenes with 1,3-Dienes: Synthesis of 3‑Allylindoles

3-Allylindoles constitute a key structural feature in many natural products and bioactive compounds. In this work, we developed a Mo-mediated reductive cyclization/allylation of 2-alkynyl nitroarenes with 1,3-dienes. Using Mo(CO)<sub>6</sub> as both the reductant and the catalyst, a broad range of functionalized 3-allylindoles were prepared in good to excellent yields from easily available 2-alkynylnitroarenes and 1,3-dienes as starting materials.

Publication Details

Journal
Figshare
Published
2025-03-28
DOI
https://doi.org/10.1021/acs.orglett.5c00624.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
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article

Mo-MediatedReductive Cyclization/Allylation of 2‑AlkynylNitroarenes with 1,3-Dienes: Synthesis of 3‑Allylindoles

Figshare
Mycorrhizal Fungi and Plant Interactions
article

Mo-MediatedReductive Cyclization/Allylation of 2‑AlkynylNitroarenes with 1,3-Dienes: Synthesis of 3‑Allylindoles

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Abstract

3-Allylindoles constitute a key structural feature in many natural products and bioactive compounds. In this work, we developed a Mo-mediated reductive cyclization/allylation of 2-alkynyl nitroarenes with 1,3-dienes. Using Mo(CO)<sub>6</sub> as both the reductant and the catalyst, a broad range of functionalized 3-allylindoles were prepared in good to excellent yields from easily available 2-alkynylnitroarenes and 1,3-dienes as starting materials.

Figshare
Openalex Percentile: Top 55%
Mycorrhizal Fungi and Plant Interactions
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Mo-MediatedReductive Cyclization/Allylation of 2‑AlkynylNitroarenes with 1,3-Dienes: Synthesis of 3‑Allylindoles · Figshare (2025) | TGRS Research Map | TGRS