Lanthanide-Catalyzed endo-Selective Hetero Diels-Alder Reactions of 4-Substituted Methyl (E)-2-Oxo-3-butenoates with Vinyl Ethers

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概要

• 論文の詳細を見る

• Methyl (E)-2-oxo-4-phenyl-, -4-methyl-, and -4-methoxy-3-butenoates as hetero 1,3-dienes undergo smooth hetero Diels-Alder reactions with vinyl ethers in the presence of a catalytic amount of lanthanide catalysts. The reactions are highly endo-selective producing 2,4-cis-3,4-dihydro-2H-pyrans in moderate to high yields, the configuration at 3-position depending on the stereochemistry of the starting vinyl ethers. Catalytic asymmetric version of this reaction was also examined by using chiral lanthanide catalysts, but enantioselectivity was not satisfactory.

• 九州大学の論文
• 1997-12-15

著者

• IMACHI Naoki

  Interdisciprinary Graduate School of Engineering Sciences, Kyushu University

• Imachi Naoki

  Interdisciprinary Graduate School Of Engineering Sciences Kyushu University

関連論文

• Lanthanide-Catalyzed endo-Selective Hetero Diels-Alder Reactions of 4-Substituted Methyl (E)-2-Oxo-3-butenoates with Vinyl Ethers

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