Three-step synthesis of α-methylene-γ-lactones through formation and oxidation of substituted cyclobutanones
Трехступенчатый синтез α-метилен-γ-лактонов посредством образования и окисления замещенных циклобутанонов
1975-01-01
SCID: 54.1/p5mavzgy
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cyclobutanone oxidationformation and oxidationsubstituted cyclobutanonesthree-step synthesisα-methylene-γ-lactones
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Abstract (AI)
S. M. Ali and S. M. Roberts, J. Chem. Soc., Chem. Commun., 1975, 887 DOI: 10.1039/C39750000887
Key Findings
1
A three-step synthetic route to α-methylene-γ-lactones is demonstrated via formation and oxidation of substituted cyclobutanones.
2
Substituted cyclobutanones serve as key intermediates whose oxidation yields α-methylene-γ-lactone products.
3
The method provides a concise sequence (three steps) for constructing α-methylene-γ-lactone scaffolds from cyclobutanone derivatives.
Research Object
Substituted cyclobutanones as intermediates in a three-step synthesis of α-methylene-γ-lactones
Research Subject
Formation and oxidation transformations of substituted cyclobutanones enabling synthesis of α-methylene-γ-lactones
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1975-01-01
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