CYCLOADDITION-REARRANGEMENT OF CYCLOHEXADIENOL ETHERS. A VERSATILE AND SELECTIVE SYNTHESIS OF CYCLOPENTENOID SYSTEMS

DOI: 10.1016/S0040-4039(00)85042-X

Source and publish data:

Tetrahedron Letters p. 4701 - 4704 (1986)

Update date:2022-09-26

Topics:

Authors:

Goldsmith, David J.

Soria, Jose J.

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Article abstract of DOI:10.1016/S0040-4039(00)85042-X

1,4-Cyclohexadienol ethers prepared by the Birch reduction of alkyl aryl ethers react at ambient pressure and moderate temperatures with p-bromobenzenesulfonyl azide to yield cyclopentenecarboximidates.The cycloaddition-rearrangement is highly specific fo

Full text of DOI:10.1016/S0040-4039(00)85042-X

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