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June 4, 2026The Journal of Organic Chemistry0 citations

Synthesis of Spirobenzo[ b thiophene-2(3 H ),1′-cyclopropan]-3-ones via Phosphine-Mediated 2 + 1 Cyclization and their Synthetic Transformations

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MXMin XiangSZShen-Xin ZhuGWGuang‐Wei Wang

Key Points

  • The aim is to develop a method for synthesizing spiro[benzo[b]thiophene-2(3H),1′-cyclopropan]-3-ones and study their synthetic transformations.
  • Phosphine-mediated [2 + 1] cyclization to form spiro compounds.
  • Subsequent derivatizations to create fused dihydrofuran or furanone scaffolds.
  • Conducted under mild conditions with a wide variety of substrates.
  • Efficient synthesis of spiro[benzo[b]thiophene-2(3H),1′-cyclopropan]-3-ones achieved through phosphine mediation.
  • Derivatization processes successfully yield valuable fused scaffolds.
  • Broad substrate scope demonstrates the versatility of the synthetic method.

Abstract

),1'-cyclopropan]-3-ones. Subsequent derivatizations underscore its practical value in constructing fused dihydrofuran- or furanone-containing scaffolds. Both the cyclization and the downstream transformations proceed under mild conditions and tolerate a broad substrate scope.

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Cite This Study

Xiang et al. (2026) studied this question.

synapsesocial.com/papers/6a211763d499ed480b17036dhttps://doi.org/10.1021/acs.joc.6c00223
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