The synthesis of the C(18)-C(34) fragment of amphidinolide C has been achieved via two routes, culminating in both the shortest (11 steps) and highest yielding (26% overall yield) approaches to this segment. The highly convergent approach will facilitate the synthesis of analogues, including the C(18)-C(29) fragment of amphidinolide F. Synthetic highlights include the selective methylation of a diyne, and the highly efficient use of a second generation cobalt catalyst in the Mukaiyama oxidative cyclization to form the trans-THF ring
International audienceAmphidinolides F, C, C2, and C3 are marine natural products isolated from dino...
The general objective of my thesis work was to achieve the synthesis of amphidinolides C2 and U, mar...
The amphidinolides are macrolide natural products isolated from marine dinoflagellates of the genus ...
The synthesis of the C(18)-C(34) fragment of amphidinolide C has been achieved via two routes, culmi...
An allylic cis-epoxide prepared by Sharpless asymmetric epoxidation was transformed in 9 steps and 4...
A second generation catalyst for the Mukaiyama oxidative cyclization for the formation of trans-THF ...
Exploration of an ambitious new strategy for the total synthesis of the cytotoxic marine natural pro...
The amphidinolides are marine macrolides extracted from dinoflagellates of the genus Amphidinium. To...
The complete carbon framework of the macrocyclic marine natural product amphidinolide F has been pre...
Nature is a pretty unselective “chemist” when it comes to making the highly cytotoxic amphidinolide ...
The amphidinolides are a family of structurally-related cytotoxic natural products which have shown ...
Orchestrated yet nonconsonant: The challenge posed by the “umpoled” 1,4-dioxygenation pattern charac...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...
Amphidinolide natural products are a family of marine macrolides, isolated from Amphidinium dinoflag...
A formal total synthesis of the cytotoxic macrolide amphidinolide E is reported. The strategic steps...
International audienceAmphidinolides F, C, C2, and C3 are marine natural products isolated from dino...
The general objective of my thesis work was to achieve the synthesis of amphidinolides C2 and U, mar...
The amphidinolides are macrolide natural products isolated from marine dinoflagellates of the genus ...
The synthesis of the C(18)-C(34) fragment of amphidinolide C has been achieved via two routes, culmi...
An allylic cis-epoxide prepared by Sharpless asymmetric epoxidation was transformed in 9 steps and 4...
A second generation catalyst for the Mukaiyama oxidative cyclization for the formation of trans-THF ...
Exploration of an ambitious new strategy for the total synthesis of the cytotoxic marine natural pro...
The amphidinolides are marine macrolides extracted from dinoflagellates of the genus Amphidinium. To...
The complete carbon framework of the macrocyclic marine natural product amphidinolide F has been pre...
Nature is a pretty unselective “chemist” when it comes to making the highly cytotoxic amphidinolide ...
The amphidinolides are a family of structurally-related cytotoxic natural products which have shown ...
Orchestrated yet nonconsonant: The challenge posed by the “umpoled” 1,4-dioxygenation pattern charac...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...
Amphidinolide natural products are a family of marine macrolides, isolated from Amphidinium dinoflag...
A formal total synthesis of the cytotoxic macrolide amphidinolide E is reported. The strategic steps...
International audienceAmphidinolides F, C, C2, and C3 are marine natural products isolated from dino...
The general objective of my thesis work was to achieve the synthesis of amphidinolides C2 and U, mar...
The amphidinolides are macrolide natural products isolated from marine dinoflagellates of the genus ...