Limitations of models in total synthesis are illustrated by a study towards the potent cytotoxic macrolide iejimalide B. Although the Yamaguchi protocol allowed for the esterification of elaborate segments, attempted macrolactonization of the seco acid met with failure (see scheme, Boc= tert-butyloxycarbonyl). The assembly of the seco acid involves some of the most advanced applications of the Julia olefination known to date
After the discovery of erythromycin and other natural compounds, including oleandomycin, spiramycin,...
The brasilinolides are an architecturally complex family of 32-membered macrolides, characterised by...
Out of the blue: The marine macrolide spirastrellolide A is a potent and selective inhibitor of prot...
Limitations of models in total synthesis are illustrated by a study towards the potent cytotoxic mac...
Metathesis to the rescue: Although counterintuitive at first sight, application of ring-closing meta...
A concise and convergent total synthesis of the highly cytotoxic marine natural products iejimalide ...
The spirastrellolides are a novel family of structurally unprecedented marine macrolides which show ...
Even though the macrolides of the iejimalide family are of marine origin, whereas those of the archa...
A formal total synthesis of the cytotoxic macrolide amphidinolide E is reported. The strategic steps...
Many natural products, including antibiotics, are structurally complex and contain a wide variety of...
The macrolide class of antibiotics has been widely used to treat bacterial infections for over 65 ye...
A concise total synthesis of spirastrellolide A methyl ester (1a, R<sup>1</sup>=Me) as the parent co...
A hypothetical Mannich macrocyclization in the biosynthesis of chejuenolides A–C served as the basis...
The brasilinolides are an architecturally complex family of 32-membered macrolides, characterised by...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
After the discovery of erythromycin and other natural compounds, including oleandomycin, spiramycin,...
The brasilinolides are an architecturally complex family of 32-membered macrolides, characterised by...
Out of the blue: The marine macrolide spirastrellolide A is a potent and selective inhibitor of prot...
Limitations of models in total synthesis are illustrated by a study towards the potent cytotoxic mac...
Metathesis to the rescue: Although counterintuitive at first sight, application of ring-closing meta...
A concise and convergent total synthesis of the highly cytotoxic marine natural products iejimalide ...
The spirastrellolides are a novel family of structurally unprecedented marine macrolides which show ...
Even though the macrolides of the iejimalide family are of marine origin, whereas those of the archa...
A formal total synthesis of the cytotoxic macrolide amphidinolide E is reported. The strategic steps...
Many natural products, including antibiotics, are structurally complex and contain a wide variety of...
The macrolide class of antibiotics has been widely used to treat bacterial infections for over 65 ye...
A concise total synthesis of spirastrellolide A methyl ester (1a, R<sup>1</sup>=Me) as the parent co...
A hypothetical Mannich macrocyclization in the biosynthesis of chejuenolides A–C served as the basis...
The brasilinolides are an architecturally complex family of 32-membered macrolides, characterised by...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
After the discovery of erythromycin and other natural compounds, including oleandomycin, spiramycin,...
The brasilinolides are an architecturally complex family of 32-membered macrolides, characterised by...
Out of the blue: The marine macrolide spirastrellolide A is a potent and selective inhibitor of prot...