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

A route for the degradation of the side chain of ent-labdane derivatives has beendevised, giving the useful synthon 2β,12-dihydroxy-13,14,15,16,17-pentanor-ent-labdane-8-one (8). The use of this compound in the preparation of terpenylquinone derivatives shallbe reported elsewhere. In addition we...

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Main Authors: María Cristina Chamy, Mauricio Cuellar Fritis, Héctor Carrasco Altamirano, Karen Catalán Marín, Luis Espinoza Catalán
Format: Article
Language:English
Published: MDPI AG 2007-12-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/12/12/2605/
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spelling doaj-54c42599402143d0a5048d2fb0b32aba2020-11-24T22:49:35ZengMDPI AGMolecules1420-30492007-12-0112122605262010.3390/12122605Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part IIMaría Cristina ChamyMauricio Cuellar FritisHéctor Carrasco AltamiranoKaren Catalán MarínLuis Espinoza CatalánA route for the degradation of the side chain of ent-labdane derivatives has beendevised, giving the useful synthon 2β,12-dihydroxy-13,14,15,16,17-pentanor-ent-labdane-8-one (8). The use of this compound in the preparation of terpenylquinone derivatives shallbe reported elsewhere. In addition we have synthesized the compound 2β,12-diacetoxy-8β,17-epoxy-13,14,15,16-tetranor-ent-labdane (10), which upon catalytic epoxide ringopening in alkaline or acid media gave rise in all cases to the formation of tricycliccompounds.http://www.mdpi.com/1420-3049/12/12/2605/Ent-labdanesselective degradationsunsaturated side chain.
collection DOAJ
language English
format Article
sources DOAJ
author María Cristina Chamy
Mauricio Cuellar Fritis
Héctor Carrasco Altamirano
Karen Catalán Marín
Luis Espinoza Catalán
spellingShingle María Cristina Chamy
Mauricio Cuellar Fritis
Héctor Carrasco Altamirano
Karen Catalán Marín
Luis Espinoza Catalán
Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
Molecules
Ent-labdanes
selective degradations
unsaturated side chain.
author_facet María Cristina Chamy
Mauricio Cuellar Fritis
Héctor Carrasco Altamirano
Karen Catalán Marín
Luis Espinoza Catalán
author_sort María Cristina Chamy
title Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
title_short Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
title_full Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
title_fullStr Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
title_full_unstemmed Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
title_sort oxidative degradations of the side chain of unsaturated ent-labdanes. part ii
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2007-12-01
description A route for the degradation of the side chain of ent-labdane derivatives has beendevised, giving the useful synthon 2β,12-dihydroxy-13,14,15,16,17-pentanor-ent-labdane-8-one (8). The use of this compound in the preparation of terpenylquinone derivatives shallbe reported elsewhere. In addition we have synthesized the compound 2β,12-diacetoxy-8β,17-epoxy-13,14,15,16-tetranor-ent-labdane (10), which upon catalytic epoxide ringopening in alkaline or acid media gave rise in all cases to the formation of tricycliccompounds.
topic Ent-labdanes
selective degradations
unsaturated side chain.
url http://www.mdpi.com/1420-3049/12/12/2605/
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