THE STEREOCHEMISTRY OF REDUCTIVE CARBOXYLATION PRODUCTS OF (1S, 8R)-1-METHYL-5, 6, 7, 8-TETRAHYDROINDAN-5-ONE

Motoo TORI; Masakazu SONO; Yoshinori ASAKAWA

doi:10.1248/cpb.37.534

著者情報

キーワード: (1S, 8R)-1-Methyl-5, 6, 7, 8-tetrahydroindan-5-one, 1, 5-dimethyl-perhydroindan-4-one, Birch reduction, reductive carboxylation

ジャーナルフリー

1989 年 37 巻 2 号 p. 534-535

DOI https://doi.org/10.1248/cpb.37.534

詳細

抄録

The title compound has been reductively carboxylated under the Birch reduction conditions. The resulting keto esters are assigned to cis and trans fused hydrindanones by transofrmations into 1, 5-dimethyl-4, 5, 6, 7, 8, 9-hexahydroindan-4-ones.

責任著者(Corresponding author)

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