Amphidinols are intriguing amphiphilic architectures exhibiting a variety of biological actions, including antifungal, hemolytic, cytotoxic and ichthyotoxic activities. These properties derive from the disturbance of the arrangement of the lipid bilayer of the targeted cells. The third member of the family, amphidinol 3 was discovered in 1996 and is, to date, the only amphidinol whose stereochemistry is fully established. The synthesis of the C15-C30 polyol domain, as well as the preparation of the C31-C40 trans-configured tetraydropyran will be discussed throughout this work.(SC - Sciences) -- UCL, 201
Amphidinolides A-V represent a family of cytotoxic marine natural products with diverse structural f...
Model compounds (11 and 12) for the C1–C10 tetrahydropyran fragment of amphidinol 2 were prepared fr...
Eureka! The first conquest of the exceptionally potent cytotoxic agent amphidinolide H, which exhibi...
Amphidinol 3 (AM3) is a polyketide-derived natural product, produced by the marine dinoflagellate Am...
Les amphidinols sont une nouvelle classe de molécules naturelles de type polycétide dont l’amphidino...
A convergent synthesis of the C31-C52 bis-tetrahydropyran core of the natural product amphidinol 3 i...
Amphidinols are a new class of polyketide extracted from dinoflagellates and exhib promising biolog...
The amphidinols (AMs) are a series of polyhydroxylated polyene compounds isolated from the dinoflage...
Amphidinol 1, a bioactive compound, was isolated from a dinoflagellate in 1991. The compound (AM1) s...
This PhD thesis was performed in the laboratory of Professor Markó, at the Chemistry Department of t...
Sharpless asymmetric dihydroxylation and Nozaki-Hiyama-Kishi's Cr(II)-mediated coupling between an &...
Stereoselective synthesis of the C43–C67 part of amphidinol 3 (AM3) and its C51-epimer was achieved ...
The total syntheses of amphidinolide B<sub>1</sub> and the proposed structure of amphidinolide B<sub...
Stereoselective synthesis of the (8S, 9S, 11R, 16S)-C<SUB>1</SUB>C<SUB>18</SUB> segment 1 of amphid...
Les amphidinols sont une nouvelle classe de molécules naturelles de type polycétide dont l amphidino...
Amphidinolides A-V represent a family of cytotoxic marine natural products with diverse structural f...
Model compounds (11 and 12) for the C1–C10 tetrahydropyran fragment of amphidinol 2 were prepared fr...
Eureka! The first conquest of the exceptionally potent cytotoxic agent amphidinolide H, which exhibi...
Amphidinol 3 (AM3) is a polyketide-derived natural product, produced by the marine dinoflagellate Am...
Les amphidinols sont une nouvelle classe de molécules naturelles de type polycétide dont l’amphidino...
A convergent synthesis of the C31-C52 bis-tetrahydropyran core of the natural product amphidinol 3 i...
Amphidinols are a new class of polyketide extracted from dinoflagellates and exhib promising biolog...
The amphidinols (AMs) are a series of polyhydroxylated polyene compounds isolated from the dinoflage...
Amphidinol 1, a bioactive compound, was isolated from a dinoflagellate in 1991. The compound (AM1) s...
This PhD thesis was performed in the laboratory of Professor Markó, at the Chemistry Department of t...
Sharpless asymmetric dihydroxylation and Nozaki-Hiyama-Kishi's Cr(II)-mediated coupling between an &...
Stereoselective synthesis of the C43–C67 part of amphidinol 3 (AM3) and its C51-epimer was achieved ...
The total syntheses of amphidinolide B<sub>1</sub> and the proposed structure of amphidinolide B<sub...
Stereoselective synthesis of the (8S, 9S, 11R, 16S)-C<SUB>1</SUB>C<SUB>18</SUB> segment 1 of amphid...
Les amphidinols sont une nouvelle classe de molécules naturelles de type polycétide dont l amphidino...
Amphidinolides A-V represent a family of cytotoxic marine natural products with diverse structural f...
Model compounds (11 and 12) for the C1–C10 tetrahydropyran fragment of amphidinol 2 were prepared fr...
Eureka! The first conquest of the exceptionally potent cytotoxic agent amphidinolide H, which exhibi...