Efficient Synthesis of Unsymmetrical 7,7′-Biindolizines

Six new unsymmetrical 7,7′-biindolizines were synthesized through an efficient metal-free [2+2+1] cycloaddition of ethyl 3-benzoyl-7-(pyridin-4-yl)indolizine-1-carboxylate with two equivalents of dimethyl acetylenedicarboxylate in methanol. The transformation involves one C≡C triple bond cleavage and provides access to previously unexplored unsymmetrical functionalized 7,7′-biindolizines.

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Publication Details

Journal
Molbank
Published
2025-10-15
DOI
https://doi.org/10.3390/m2074
Citations
1
Primary Topic
Synthesis and Reactivity of Heterocycles
Type
article
Field-Weighted Citation Impact
0.94
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article

Efficient Synthesis of Unsymmetrical 7,7′-Biindolizines

Roxana Ciorteanu, Ramona Danac, Ionel I. Mangalagiu, Ioana Radu et al.
1 citations
Molbank
Synthesis and Reactivity of Heterocycles
0.94
article

Efficient Synthesis of Unsymmetrical 7,7′-Biindolizines

Roxana Ciorteanu, Ramona Danac, Ionel I. Mangalagiu, Ioana Radu, Catalina Ionica Ciobanu, Andreea Danila
article en
1 citations

Abstract

Six new unsymmetrical 7,7′-biindolizines were synthesized through an efficient metal-free [2+2+1] cycloaddition of ethyl 3-benzoyl-7-(pyridin-4-yl)indolizine-1-carboxylate with two equivalents of dimethyl acetylenedicarboxylate in methanol. The transformation involves one C≡C triple bond cleavage and provides access to previously unexplored unsymmetrical functionalized 7,7′-biindolizines.

MolbankVol. 2025(4)
Alexandru Ioan Cuza University (RO)
Openalex Percentile: Top 20%
Synthesis and Reactivity of Heterocycles
0.94
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