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April 18, 2026Organics1 citationsOpen Access

Revised Formal Total Synthesis of Dehydro-δ-Viniferin and Anigopreissin A

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ASAlessandro SantarsiereMVMarianna VolgareLCLucia Chiummiento

Key Points

  • The goal is to refine the total synthesis process of two important benzofurans using environmentally friendly techniques.
  • Developed new synthetic routes to stilbene dimers.
  • Optimized Sonogashira coupling in water.
  • Conducted a Suzuki-like reaction in dimethyl carbonate without transition metals.
  • Achieved synthesis of benzofuran core under milder reaction conditions.
  • Demonstrated environmentally friendly methodologies in the synthesis process.

Abstract

This work presents a revised total synthesis of two pharmacologically relevant benzofurans using newly developed environmentally friendly methodologies. In particular, we focused on establishing improved synthetic routes to stilbene dimers under milder and more sustainable reaction conditions. During our investigations, we optimized an efficient Sonogashira coupling carried out in water, which, followed by a Suzuki-like reaction conducted in dimethyl carbonate (DMC) in the absence of any transition metals, served as the key step for the synthesis of the benzofuran core.

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Cite This Study

Santarsiere et al. (2026) studied this question.

synapsesocial.com/papers/69e3216540886becb65409d1https://doi.org/10.3390/org7020017
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Total Synthesis of the Oligostilbenes Anigopreissin A and Fuliginosin A2026
  2. 2Stereochemical Revision and First Total Synthesis of Renifolin D2026
  3. 3Enantioselective Total Synthesis of (+)-Propolisbenzofuran B2024
  4. 4Green approaches in the synthesis and reactivity of benzofuran derivatives: a comprehensive review2026
  5. 5Enantioselective Total Synthesis of (+)‐Propolisbenzofuran B<sup>†</sup>2024