Add to ORKGAn anionic oxy-Cope/transannular Michael addition cascade converts a spirocyclic architecture-readily available by Diels-Alder cycloaddition-into the hydrophenalene carbon skeleton of the pseudopterosin aglycones. Oxidation of the resulting cyclohexenone ring to the phenol that is characteristic of the targets completes a short formal synthesis
A synthesis of a tricyclic intermediate for platencin from a simple aromatic precursor is described....
Cyclization of an aryl radical at the ipso position of a p-O-aryl-substituted acetamide or benzamide...
This thesis details the application of two synthetic methodologies, developed by the Donohoe group, ...
A synthetic approach to the Pseudopterosins, a family of marine natural products which display poten...
The stereocontrolled and efficient syntheses of the aglycones of the potent anti-inflammatory pseudo...
A short and practical route to the tricyclic core of an unnatural pseudopterosin diastereoisomer is ...
This thesis is concerned with the total synthesis of natural products isolated from the Caribbean se...
Covering up to 2015: The pseudopterosin natural products have been the focus of a substantial number...
The pseudopterosins are a family of diterpene marine natural products, which, by virtue of their int...
International audienceThe formal synthesis of (–)‐PHTX is described. Our approach was based on the a...
A substrate-controlled asymmetric Prins/Conia-ene cascade cyclization has been developed with In(OTf...
[formula: see text] Both in vivo and in vitro techniques have been developed to test putative interm...
Pseudopeptidic cages have been efficiently prepared by combining a dynamic covalent procedure with t...
International audience(Matrix presented) A short synthesis of the tricyclic skeleton of pleuromutili...
This thesis is concerned with the synthesis of natural products isolated from the Caribbean Sea whip...
A synthesis of a tricyclic intermediate for platencin from a simple aromatic precursor is described....
Cyclization of an aryl radical at the ipso position of a p-O-aryl-substituted acetamide or benzamide...
This thesis details the application of two synthetic methodologies, developed by the Donohoe group, ...
A synthetic approach to the Pseudopterosins, a family of marine natural products which display poten...
The stereocontrolled and efficient syntheses of the aglycones of the potent anti-inflammatory pseudo...
A short and practical route to the tricyclic core of an unnatural pseudopterosin diastereoisomer is ...
This thesis is concerned with the total synthesis of natural products isolated from the Caribbean se...
Covering up to 2015: The pseudopterosin natural products have been the focus of a substantial number...
The pseudopterosins are a family of diterpene marine natural products, which, by virtue of their int...
International audienceThe formal synthesis of (–)‐PHTX is described. Our approach was based on the a...
A substrate-controlled asymmetric Prins/Conia-ene cascade cyclization has been developed with In(OTf...
[formula: see text] Both in vivo and in vitro techniques have been developed to test putative interm...
Pseudopeptidic cages have been efficiently prepared by combining a dynamic covalent procedure with t...
International audience(Matrix presented) A short synthesis of the tricyclic skeleton of pleuromutili...
This thesis is concerned with the synthesis of natural products isolated from the Caribbean Sea whip...
A synthesis of a tricyclic intermediate for platencin from a simple aromatic precursor is described....
Cyclization of an aryl radical at the ipso position of a p-O-aryl-substituted acetamide or benzamide...
This thesis details the application of two synthetic methodologies, developed by the Donohoe group, ...