A synthesis of the C8–C29 fragment of amphidinolide N, a potent cytotoxic macrolide isolated from the marine dinoflagellate Amphidinium sp., has been achieved. The key features of the synthesis involve a convergent union of the C9–C15 and C16–C29 fragments by Steglich esterification and the construction of a pyran unit through a Tebbe methylenation/ring-closing metathesis sequence
An asymmetric synthesis of a diastereomer (2) of the structure (1) proposed for amphidinolide A, a c...
Exploration of an ambitious new strategy for the total synthesis of the cytotoxic marine natural pro...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...
Amphidinolide O (1) was isolated from the laboratory cultured Okinawan marine dinoflagelate amphidin...
Studies towards the total synthesis of the cytotoxic marine macrolide Amphidinolide B have been disc...
Les amphidinolides C et F sont des macrocycles isolés de dinoflagellés Amphidinium sp. vivant en sym...
b-Hydroxy aldehyde and alkyl ketone moieties were effectively synthesized as key intermediates of am...
International audienceAmphidinolides F, C, C2, and C3 are marine natural products isolated from dino...
A concise total synthesis of the cytotoxic marine natural product amphidinolide X (1) is described. ...
L'objectif général de mon travail de thèse a été de réaliser la synthèse des amphidinolides C2 et U,...
The dinoflagellates are marine organisms (phytoplancton) that have shown to be a major source of tox...
The amphidinolides are a family of structurally-related cytotoxic natural products which have shown ...
Abstract An asymmetric synthesis of a diastereomer (2) of the structure (1) proposed for amphidinoli...
The general objective of my thesis work was to achieve the synthesis of amphidinolides C2 and U, mar...
Nature is a pretty unselective “chemist” when it comes to making the highly cytotoxic amphidinolide ...
An asymmetric synthesis of a diastereomer (2) of the structure (1) proposed for amphidinolide A, a c...
Exploration of an ambitious new strategy for the total synthesis of the cytotoxic marine natural pro...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...
Amphidinolide O (1) was isolated from the laboratory cultured Okinawan marine dinoflagelate amphidin...
Studies towards the total synthesis of the cytotoxic marine macrolide Amphidinolide B have been disc...
Les amphidinolides C et F sont des macrocycles isolés de dinoflagellés Amphidinium sp. vivant en sym...
b-Hydroxy aldehyde and alkyl ketone moieties were effectively synthesized as key intermediates of am...
International audienceAmphidinolides F, C, C2, and C3 are marine natural products isolated from dino...
A concise total synthesis of the cytotoxic marine natural product amphidinolide X (1) is described. ...
L'objectif général de mon travail de thèse a été de réaliser la synthèse des amphidinolides C2 et U,...
The dinoflagellates are marine organisms (phytoplancton) that have shown to be a major source of tox...
The amphidinolides are a family of structurally-related cytotoxic natural products which have shown ...
Abstract An asymmetric synthesis of a diastereomer (2) of the structure (1) proposed for amphidinoli...
The general objective of my thesis work was to achieve the synthesis of amphidinolides C2 and U, mar...
Nature is a pretty unselective “chemist” when it comes to making the highly cytotoxic amphidinolide ...
An asymmetric synthesis of a diastereomer (2) of the structure (1) proposed for amphidinolide A, a c...
Exploration of an ambitious new strategy for the total synthesis of the cytotoxic marine natural pro...
International audienceA new and efficient convergent approach toward the synthesis of amphidinolide ...