Publication | Closed Access
Synthesis and Biological Activity of α‐Methylene‐γ‐butyrolactones
644
Citations
143
References
1985
Year
Biological ActivityNucleophilic AttackDiversity Oriented SynthesisBioorganic ChemistryEngineeringBiochemistryNatural SciencesDiversity-oriented SynthesisOrganic ChemistryNatural ProductsUnusual 1,4‐FunctionalityChemistryHeterocycle ChemistryNatural Product SynthesisSynthetic ChemistryEnantioselective Synthesis
Abstract α‐Methylene‐γ‐butyrolactones [dihydro‐3‐methylene‐2(3 H )furanones] constitute an important group of natural products and possess wide‐ranging biological activities. Progress in the synthesis of the heterocycle and the classification of the synthetic methods are not only of practical interest, but also fundamentally important as a current example for the construction of an unusual 1,4‐functionality distance and an α‐substituted acrylic ester moiety which is susceptible to nucleophilic attack.
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