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Molecules 2007, 12(3), 318-327; doi:10.3390/12030318

Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part I.

Departamento de Química, Universidad Técnica Federico Santa María, Av. España N° 1680, Valparaíso, Chile
Departamento de Ciencias Químicas, Universidad Andrés Bello, Campus Viña del Mar, Los Fresnos N° 52, Viña del Mar, Chile
Facultad de Farmacia, Universidad de Valparaíso, Av. Gran Bretaña N° 1093, Valparaíso, Chile
Author to whom correspondence should be addressed.
Received: 22 November 2006 / Revised: 19 January 2007 / Accepted: 24 January 2007 / Published: 6 March 2007
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A selective route for the degradation of the unsaturated side chain of ent-labdanes has been devised, giving two useful synthons: 2β-acetoxy-14,15,17-trinor-ent-labdane-8,13- dione (5) and 2β-acetoxy-14,15-dinor-ent-labd-8(17)-en-13-one (7), the use of which for the preparation of terpenylquinone derivatives shall be reported elsewhere. View Full-Text
Keywords: Ent-labdanes; selective degradations; unsaturated side chain Ent-labdanes; selective degradations; unsaturated side chain

Figure 1

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Catalán, L.E.; Altamirano, H.C.; Fritis, M.C.; Araya, C.G.; Marín, K.C. Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part I.. Molecules 2007, 12, 318-327.

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