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1972•Australian Journal of ChemistryRequires access

Chemistry of the Podocarpaceae. XXXVIII. Reduced ring-c transformations of 12-Methoxypodocarpa-8,11,13-trien- 19-ol

RC Cambie, AW Missen

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Abstract

Birch-type reductions of 12-methoxypodocarpa-8,11,13-trien-19-01 (2) have been investigated and the products have been converted into the 13-oxo derivatives (7) and (30) which have potential use as chiral intermediates for synthesis. The C14 ketone (9) which is also of potential value, has been prepared from the reduced derivative, methyl 12-oxopodocarp-13-en-19-oate (21).

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What this paper is about

Birch-type reductions of 12-methoxypodocarpa-8,11,13-trien-19-01 (2) have been investigated and the products have been converted into the 13-oxo derivatives (7) and (30) which have potential use as chiral intermediates for synthesis. The C14 ketone (9) which is also of potential value, has been prepared from the reduced derivative, methyl 12-oxopodocarp-13-en-19-oate (21).

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Available abstract

Birch-type reductions of 12-methoxypodocarpa-8,11,13-trien-19-01 (2) have been investigated and the products have been converted into the 13-oxo derivatives (7) and (30) which have potential use as chiral intermediates for synthesis. The C14 ketone (9) which is also of potential value, has been prepared from the reduced derivative, methyl 12-oxopodocarp-13-en-19-oate (21).

Key concepts: Biocatalysis, Chemistry, Green chemistry, Ring (chemistry), Ketone, Podocarpaceae, Reaction mechanism, Supramolecular chemistry

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Chemistry of the Podocarpaceae. XXXVIII. Reduced ring-c transformations of 12-Methoxypodocarpa-8,11,13-trien- 19-ol — Research Paper | ScholarLens