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Updated: Feb 12, 2026
![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)
The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Anionic Annulation of 3-Cyanophthalides with Allene Carboxylates: A Carbon-Conserved Synthesis of Naphtho[
Supriti Jana1, Dipakranjan Mal1
1Department of Chemistry , Indian Institute of Technology Kharagpur , 721302 , India.
Abstract:
The reaction of 3-cyanophthalides with allene carboxylates in the presence of tBuOLi results in a tandem annulation furnishing naphtho[ b]furanones in good yields with no loss of carbon. The carbon economy is explained by a tandem process, in which the initially expelled cyanide induces the second annulation.
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