Competitive Intramolecular Cycloaddition and Tandem Cycloaddition/-Sigmatropic Rearrangement Sequence of Allenyl 3-Vinyl-2-cyclohexenyl Ethers: Evidence for Switching of the Reaction Pathway by the Substituent Effects

DOI: 10.1021/ja00196a041

Source and publish data:

Journal of the American Chemical Society p. 5312 - 5320 (1989)

Update date:2022-08-05

Topics: Substituent Effects

Authors:

Hayakawa, Kenji

Aso, Kazuyoshi

Shiro, Motoo

Kanematsu, Ken

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Article abstract of DOI:10.1021/ja00196a041

The base-catalyzed intramolecular cycloaddition reactions (t-BuOK, t-BuOH, 83 deg C) of variously substituted propargyl 3-vinyl-2-cyclohexenyl ethers have been investigated.The reaction proceeded smoothly via the initial isomerization to the corresponding

Full text of DOI:10.1021/ja00196a041

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