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Communication | Regular issue | Vol 23, No. 1, 1985, pp.41-44
Published online, 1st January, 1970
DOI: 10.3987/R-1985-01-0041
Stereoselective Formation of a Cyclopentanoid with Three Contiguous Substituents via Inrtamolecular Cycloaddition

Seiichi Takano,* Shigeki Satoh, and Kunio Ogasawara

*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan


A stereoselective formation of a cyclopentanoid with three contiguous substituents has been demonstrated by using a linear aldehyde and Meldrum’s acid via an intramolecular cycloaddition.