Javascript must be enabled to continue!
(+)-Podocarpic Acid as Chiral Template in the Synthesis of Aphidicolane, Stemodane and Stemarane Diterpenoids †
View through CrossRef
In this review the synthetic work in the field of aphidicolane, stemodane and stemarane diterpenoids, in which readily available (+)-podocarpic acid (4) was used as chiral template for the construction of their polycyclic structures, is described as it developed along the years. In the frame of this work (+)-podocarpic acid (4) was a very useful tool in a model study leading to the syntheses of tetracyclic ketones 7 and 8, models of key intermediates 5a and 6 in the syntheses of (+)-aphidicolin (1) and (+)-stemodin (2a), respectively. (+)-Podocarpic acid (4) was also converted into (+)-2-deoxystemodinone (2d), allowing confirmation of the stemodane diterpenoids absolute configuration, into (+)-aphidicol-15-ene (36) and into Stemodia chilensis tetracyclic diterpenoid (+)-19-acetoxystemodan-12-ol (2f), allowing confirmation of its structure. (+)-Podocarpic acid (4) was then extensively used in the work which led to the synthesis of (+)-stemar-13-ene (57) and (+)-18-deoxystemarin (3b). Finally, (+)-4 was converted into (+)-2-deoxyoryzalexin S (66), which made it possible to demonstrate that the structure of (+)-66 could not be attributed to a Chilean Calceolaria isolated diterpenoid to which this structure had been assigned.
Title: (+)-Podocarpic Acid as Chiral Template in the Synthesis of Aphidicolane, Stemodane and Stemarane Diterpenoids †
Description:
In this review the synthetic work in the field of aphidicolane, stemodane and stemarane diterpenoids, in which readily available (+)-podocarpic acid (4) was used as chiral template for the construction of their polycyclic structures, is described as it developed along the years.
In the frame of this work (+)-podocarpic acid (4) was a very useful tool in a model study leading to the syntheses of tetracyclic ketones 7 and 8, models of key intermediates 5a and 6 in the syntheses of (+)-aphidicolin (1) and (+)-stemodin (2a), respectively.
(+)-Podocarpic acid (4) was also converted into (+)-2-deoxystemodinone (2d), allowing confirmation of the stemodane diterpenoids absolute configuration, into (+)-aphidicol-15-ene (36) and into Stemodia chilensis tetracyclic diterpenoid (+)-19-acetoxystemodan-12-ol (2f), allowing confirmation of its structure.
(+)-Podocarpic acid (4) was then extensively used in the work which led to the synthesis of (+)-stemar-13-ene (57) and (+)-18-deoxystemarin (3b).
Finally, (+)-4 was converted into (+)-2-deoxyoryzalexin S (66), which made it possible to demonstrate that the structure of (+)-66 could not be attributed to a Chilean Calceolaria isolated diterpenoid to which this structure had been assigned.
Related Results
Stemarane Diterpenes and Diterpenoids
Stemarane Diterpenes and Diterpenoids
In this article the scientific activity carried out on stemarane diterpenes and diterpenoids, isolated over the world from various natural sources, was reviewed. The structure eluc...
Research Progress of Diterpenoids with Potential Antidiabetic Activity
Research Progress of Diterpenoids with Potential Antidiabetic Activity
Introduction:
Diabetes mellitus has become a global epidemic. Diterpenoids have complex
and variable structures and are widely distributed in nature. They play a crucial role in di...
Advances on broadband and resonant chiral metasurfaces
Advances on broadband and resonant chiral metasurfaces
Abstract
Chirality describes mirror symmetry breaking in geometric structures or certain physical quantities. The interaction between chiral structure and chiral ...
Chiral Ionic Liquids as Stationary Phases in Electrophoretic Separations
Chiral Ionic Liquids as Stationary Phases in Electrophoretic Separations
Ionic liquids (ILs) are exceptional solvents having melting points at or
below 100 0C. They are completely made up of ions, often consisting of an organic
cation and an inorganic o...
Design, synthesis and evaluation in enantioselective catalysis of diverse adjustable axially chiral biphenyl ligands and catalysts
Design, synthesis and evaluation in enantioselective catalysis of diverse adjustable axially chiral biphenyl ligands and catalysts
Chiral compounds widely occur in biomolecules, natural products and drugs, and acquisition of chirality in the chiral molecules highly depends on chiral inducers including chiral l...
Chiral liquid crystal-MOF composites for electrochemical recognition of enantiomers
Chiral liquid crystal-MOF composites for electrochemical recognition of enantiomers
Biological systems rely on the exclusive use of L-configured biomolecules for precise molecular recognition, whereas exposure to D-enantiomers can disrupt immune and metabolic proc...
Laminar and Turbulent Dynamos in Chiral Magnetohydrodynamics. I. Theory
Laminar and Turbulent Dynamos in Chiral Magnetohydrodynamics. I. Theory
Abstract
The magnetohydrodynamic (MHD) description of plasmas with relativistic particles necessarily includes an additional new field, the chiral chemical potential...
Chiral Ionic Liquids and Chromatography: Synergistic Effects in Enantioseparations
Chiral Ionic Liquids and Chromatography: Synergistic Effects in Enantioseparations
Chiral ionic liquids (CILs) are a subcategory of ionic liquids that possess a
chiral moiety. The need for chiral separations in several industries, including
pharmaceutical, food, ...

