CYCLOADDITION-REARRANGEMENT OF CYCLOHEXADIENOL ETHERS. A VERSATILE AND SELECTIVE SYNTHESIS OF CYCLOPENTENOID SYSTEMS
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
Goldsmith, David J.,Soria, Jose J.
p. 4701 - 4704
(2007/10/02)
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