A concise total synthesis of the neoclerodane diterpene salvinorin A from 3-furaldehyde is reported using two highly diastereoselective intramolecular Diels–Alder reactions (IMDA) as the key transformations
The natural neoclerodane salvinorin A exhibits a great affinity for kappa opioid receptors. Several ...
La salvinorine A est un néoclérodane naturel possédant une forte affinité pour les récepteurs opioïd...
The enantiomerically pure cis-1,2-dihydrocatechol 6, which is readily obtained via the whole-cell bi...
Diterpenes are a structural class of molecules that are derived from four isoprene subunits and are ...
Herein, we report our progress toward the total synthesis of salvadione-A, a structurally complex tr...
Transformations that selectively modify the furan ring present in a variety of naturals products wou...
This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and fl...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
Transformations that selectively modify the furan ring present in a variety of naturals products wou...
Salvinorin A 1, a psychoactive neoclerodane diterpenoid from the Mexican sage S. divinorum, has gain...
Diels-Alder (D-A) reaction is undoubtedly the most powerful [4 + 2] cycloaddition reaction in organi...
Salvinorin A 1, a psychoactive neoclerodane diterpenoid from the Mexican sage S. divinorum, has gain...
Salvinorin A is the active compound in the plant Salvia divinorum, commonly known as salvia. It is ...
A new synthetic route to (-)-neocosmosin A was devised by elaboration, of intramolecular Diels- Alde...
A total synthesis of the caribenol A (1), a novel natural product with an intriguing tetracyclic fra...
The natural neoclerodane salvinorin A exhibits a great affinity for kappa opioid receptors. Several ...
La salvinorine A est un néoclérodane naturel possédant une forte affinité pour les récepteurs opioïd...
The enantiomerically pure cis-1,2-dihydrocatechol 6, which is readily obtained via the whole-cell bi...
Diterpenes are a structural class of molecules that are derived from four isoprene subunits and are ...
Herein, we report our progress toward the total synthesis of salvadione-A, a structurally complex tr...
Transformations that selectively modify the furan ring present in a variety of naturals products wou...
This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and fl...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
Transformations that selectively modify the furan ring present in a variety of naturals products wou...
Salvinorin A 1, a psychoactive neoclerodane diterpenoid from the Mexican sage S. divinorum, has gain...
Diels-Alder (D-A) reaction is undoubtedly the most powerful [4 + 2] cycloaddition reaction in organi...
Salvinorin A 1, a psychoactive neoclerodane diterpenoid from the Mexican sage S. divinorum, has gain...
Salvinorin A is the active compound in the plant Salvia divinorum, commonly known as salvia. It is ...
A new synthetic route to (-)-neocosmosin A was devised by elaboration, of intramolecular Diels- Alde...
A total synthesis of the caribenol A (1), a novel natural product with an intriguing tetracyclic fra...
The natural neoclerodane salvinorin A exhibits a great affinity for kappa opioid receptors. Several ...
La salvinorine A est un néoclérodane naturel possédant une forte affinité pour les récepteurs opioïd...
The enantiomerically pure cis-1,2-dihydrocatechol 6, which is readily obtained via the whole-cell bi...
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