Synthetic Studies Towards the ent-Labdane Diterpenoids: Rearrangement of ent-Halimanes
For the first time ent-labdanes have been synthetised starting from ent-halimic acid, following a route that is the reverse of the biosynthetic one leading to the former compounds.
Main Authors: | Julio G. Urones, David DÃÂez, Pilar Basabe, Marta Corrales, Felix A. Hernández, MarÃÂa J. Sexmero, Isidro S. Marcos |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2006-10-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/11/10/792/ |
Similar Items
-
Synthesis of an ent-Halimanolide from ent-Halimic Acid
by: Julio G. Urones, et al.
Published: (2008-05-01) -
Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part I.
by: Karen Catalán MarÃÂn, et al.
Published: (2007-03-01) -
Halimanes and cancer: ent-halimic acid as a starting material for the synthesis of antitumor drugs
by: Alejandro M. Roncero, et al.
Published: (2023-08-01) -
Synthesis of Two New Hemisynthetic Diterpenylhydroquinones from Natural Ent-Labdanes
by: Mauricio Cuellar Fritis, et al.
Published: (2009-06-01) -
A New ent-Clerodane Diterpene from Hymenaea courbaril var. altissima
by: Nogueira Raquel T., et al.
Published: (2002-01-01)