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An Efficient Synthesis of Highly Functionalized and Electron-Deficient 1,3-Dienes from Cyclobutene Derivatives
Asian Journal of Chemistry,
Vol. 22 No. 1 (2010): Vol 22 Issue 1, 2010
Abstract
Cyclobutene derivatives undergo electrocyclic ring-opening reactions
in boiling toluene to produce highly electron-deficient 1,3-dienes. These
cyclobutenes prepare from the reaction of 2-thenoyltrifluoroacetone in
presence of triphenyl phosphine at room temperature, via intramolecular
Wittig reaction.
in boiling toluene to produce highly electron-deficient 1,3-dienes. These
cyclobutenes prepare from the reaction of 2-thenoyltrifluoroacetone in
presence of triphenyl phosphine at room temperature, via intramolecular
Wittig reaction.
Keywords
2-Thenoyltrifluoroacetone
Cyclobutene derivatives
Electrocyclic ring opening
Electron-deficient 1
3-dienes.
BAHARFAR*, R., VAHDAT, S., & BAGHBANIAN, S. (2024). An Efficient Synthesis of Highly Functionalized and Electron-Deficient 1,3-Dienes from Cyclobutene Derivatives. Asian Journal of Chemistry, 22(1), 435–438. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/16700
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