Metathesis to the rescue: Although counterintuitive at first sight, application of ring-closing metathesis (RCM) to a cyclization precursor containing 10 double bonds has led to the selective and high-yielding formation of the macrocyclic core of iejimalide B, a potent cytotoxic agent of marine origin. In contrast, a macrolactonization approach failed to afford this intricate target
New synthetic strategies directed toward the novel cyclopeptides solomonamides have been explored ut...
Macrocyclic compounds are central to the development of new drugs, but preparing them can be challen...
The stereoselective total synthesis of cytotoxic marine macrolide callyspongiolide has been reported...
Metathesis to the rescue: Although counterintuitive at first sight, application of ring-closing meta...
The macrocyclic core of the cytotoxic marine natural product callyspongiolide (1) was forged by ring...
A concise and convergent total synthesis of the highly cytotoxic marine natural products iejimalide ...
Iriomoteolides are novel macrolides possessing either a unique 15-membered or a 20-membered macrocyc...
Even though the macrolides of the iejimalide family are of marine origin, whereas those of the archa...
A concise synthesis of the putative structure assigned to the highly cytotoxic marine macrolide mand...
Limitations of models in total synthesis are illustrated by a study towards the potent cytotoxic mac...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
A stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A has been performed...
The increasing resistance to antibiotics is becoming a major threat to public health. An increasing ...
A stereocontrolled total synthesis of the microfilament-destabilizing cytotoxic macrolide (−)-reidis...
The first total synthesis of the potent antibiotic disciformycin B (2) is described, which is except...
New synthetic strategies directed toward the novel cyclopeptides solomonamides have been explored ut...
Macrocyclic compounds are central to the development of new drugs, but preparing them can be challen...
The stereoselective total synthesis of cytotoxic marine macrolide callyspongiolide has been reported...
Metathesis to the rescue: Although counterintuitive at first sight, application of ring-closing meta...
The macrocyclic core of the cytotoxic marine natural product callyspongiolide (1) was forged by ring...
A concise and convergent total synthesis of the highly cytotoxic marine natural products iejimalide ...
Iriomoteolides are novel macrolides possessing either a unique 15-membered or a 20-membered macrocyc...
Even though the macrolides of the iejimalide family are of marine origin, whereas those of the archa...
A concise synthesis of the putative structure assigned to the highly cytotoxic marine macrolide mand...
Limitations of models in total synthesis are illustrated by a study towards the potent cytotoxic mac...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
A stereoselective synthesis of the cytotoxic 14-membered macrolide aspergillide A has been performed...
The increasing resistance to antibiotics is becoming a major threat to public health. An increasing ...
A stereocontrolled total synthesis of the microfilament-destabilizing cytotoxic macrolide (−)-reidis...
The first total synthesis of the potent antibiotic disciformycin B (2) is described, which is except...
New synthetic strategies directed toward the novel cyclopeptides solomonamides have been explored ut...
Macrocyclic compounds are central to the development of new drugs, but preparing them can be challen...
The stereoselective total synthesis of cytotoxic marine macrolide callyspongiolide has been reported...