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4-Aminoindoles as 1,4-bisnucleophiles for diversity-oriented synthesis of tricyclic indoles bearing 3,4-fused seven-membered rings

Abstract : A straightforward access to tricyclic indoles bearing 3,4-fused seven-membered rings has been established by using 4-aminoindoles as 1,4-bisnucleophiles in three-component reactions. 1H-Azepino[4,3,2-cd]indoles, 4,6-dihydro-1H-azepino[4,3,2-cd]indoles and 1,3,4,6-tetrahydro-5H-azepino[4,3,2-cd]indol-5-ones could thus be synthesized in one pot in moderate to good yields. Beyond opening access to 3,4-fused tricyclic indoles, the use of easily accessible 4-aminoindoles as C,N-1,4-bisnucleophiles also provides a new platform to be used in a diversity-oriented synthesis strategy, fully displaying its benefits of maximizing molecular complexity and reaction diversity.
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https://hal-udl.archives-ouvertes.fr/hal-02193173
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Submitted on : Tuesday, July 7, 2020 - 4:24:27 PM
Last modification on : Thursday, July 9, 2020 - 3:37:17 AM

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Shaomin Chen, Palanisamy Ravichandiran, Ahmed El-Harairy, Yves Queneau, Minghao Li, et al.. 4-Aminoindoles as 1,4-bisnucleophiles for diversity-oriented synthesis of tricyclic indoles bearing 3,4-fused seven-membered rings. Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2019, 17 (24), pp.5982-5989. ⟨10.1039/C9OB01045A⟩. ⟨hal-02193173⟩

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