Lewis Acid Catalyzed Cycloaddition of Methyl 2,3-Butadienoate to Alkenes

DOI: 10.1021/jo01313a002

Source and publish data:

Journal of Organic Chemistry p. 5017 - 5020 (1980)

Update date:2022-08-02

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Authors:

Snider, Barry B.

Spindell, David K.

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Article abstract of DOI:10.1021/jo01313a002

Methyl 2,3-butadienoate (1) undergoes EtAlCl2-catalyzed stereospecific <2 + 2> cycloadditions with alkenes to give methyl cyclobutylideneacetates in good yield.The stereospecificity and ratios of E and Z isomers suggest a <_?2_s + View More

Full text of DOI:10.1021/jo01313a002

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