ChemInform Abstract: Intermediates of Prostanoid Synthesis: Stereospecific Conversion of (+)‐5β‐Hydroxycyclopenten‐2‐yl‐1β‐acetic Acid γ‐Lactone into (+)‐1β‐Methoxycarbonylmethyl‐2β,3β‐(p‐nitrobenzylidene)‐dioxycyc# lopentan‐5‐one.

Freimanis, J.; Gerca, L.; Turovskis, I.; Liepiņš, Edvards; Lola, Daina; Mishnev, Anatoly; Bundule, M. F.; Bleidelis, J.

doi:10.1002/chin.198727111

ChemInform

1987

DOI: 10.1002/chin.198727111

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ChemInform Abstract: Intermediates of Prostanoid Synthesis: Stereospecific Conversion of (+)‐5β‐Hydroxycyclopenten‐2‐yl‐1β‐acetic Acid γ‐Lactone into (+)‐1β‐Methoxycarbonylmethyl‐2β,3β‐(p‐nitrobenzylidene)‐dioxycyc# lopentan‐5‐one.

J. Freimanis¹,

L. Gerca²,

I. Turovskis³

et al.

Abstract: The title compound (I) is converted stereospecifically to the diol (II).

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ChemInform Abstract: Intermediates of Prostanoid Synthesis: Stereospecific Conversion of (+)‐5β‐Hydroxycyclopenten‐2‐yl‐1β‐acetic Acid γ‐Lactone into (+)‐1β‐Methoxycarbonylmethyl‐2β,3β‐(p‐nitrobenzylidene)‐dioxycyc# lopentan‐5‐one.

Abstract: The title compound (I) is converted stereospecifically to the diol (II).

Cited by 0 publications

References 1 publication

No citations

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