Y. Kayaki, T. Koda, T. Ikariya
Mar 4, 2004
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Journal
The Journal of organic chemistry
Abstract
The triphenyl phosphite-palladium complex was found to effect catalytic substitution reactions of allylic alcohols via a direct C-O bond cleavage. The dehydrative etherification proceeded efficiently without any cocatalysts and bases to give allylic ethers in good to excellent yields.