The enantioselective synthesis of a number of simplified analogues of the cytotoxic natural product eleutherobin is reported. © 2009 Elsevier Ltd. All rights reserved
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcod...
An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step...
A short enantioselective synthesis of (+)-eleutherin, (+)-allo-eleutherin and the formal synthesis o...
The enantioselective synthesis of a simplified eleutherobin analogue by ring closing metathesis (RCM...
Eleutherobin (1.1) has previously been shown to be comparable with paclitaxel, a multi-million dolla...
Eleutherobin is a cytotoxic agent with microtubule stabilizing properties. A formal total synthesis...
Eleutherobin and dictyostatin are antimitotic compounds which exert their cytotoxic activity by a ta...
A practical synthesis of fully functionalized 'C' ring equivalent of cytotoxic marine natural produc...
The synthesis of a number of novel simplified eleutheside analogs with potent tubulin-assembling and...
This thesis describes synthetic studies towards the tricyclic terpene framework of the cytotoxic nat...
This thesis describes synthetic studies towards the tricyclic terpene framework of the cytotoxic nat...
Asymmetric oxyallylation reactions and ring-closing metathesis have been used to synthesize compound...
A short and efficient RCM route is reported for the construction of the key nine-membered B ring of ...
A seven‐step synthesis of the first tricyclic intermediate in Danishefsky's total synthesis of eleut...
The synthesis of a number of novel, simplified, C-7 substituted eleutheside analogues with potent tu...
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcod...
An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step...
A short enantioselective synthesis of (+)-eleutherin, (+)-allo-eleutherin and the formal synthesis o...
The enantioselective synthesis of a simplified eleutherobin analogue by ring closing metathesis (RCM...
Eleutherobin (1.1) has previously been shown to be comparable with paclitaxel, a multi-million dolla...
Eleutherobin is a cytotoxic agent with microtubule stabilizing properties. A formal total synthesis...
Eleutherobin and dictyostatin are antimitotic compounds which exert their cytotoxic activity by a ta...
A practical synthesis of fully functionalized 'C' ring equivalent of cytotoxic marine natural produc...
The synthesis of a number of novel simplified eleutheside analogs with potent tubulin-assembling and...
This thesis describes synthetic studies towards the tricyclic terpene framework of the cytotoxic nat...
This thesis describes synthetic studies towards the tricyclic terpene framework of the cytotoxic nat...
Asymmetric oxyallylation reactions and ring-closing metathesis have been used to synthesize compound...
A short and efficient RCM route is reported for the construction of the key nine-membered B ring of ...
A seven‐step synthesis of the first tricyclic intermediate in Danishefsky's total synthesis of eleut...
The synthesis of a number of novel, simplified, C-7 substituted eleutheside analogues with potent tu...
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcod...
An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step...
A short enantioselective synthesis of (+)-eleutherin, (+)-allo-eleutherin and the formal synthesis o...
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