An attractive intermediate in the total synthesis of eleutherobin has been synthesised. The key step of this synthesis is an intramolecular Diels-Alder reaction, which leads to intermediate possessing rings A and C of the eleutherobin skeleton
The intramolecular Diels-Alder reaction is widely recognized as a powerful and versatile method for ...
Eleutherobin and dictyostatin are antimitotic compounds which exert their cytotoxic activity by a ta...
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcod...
An attractive intermediate in the total synthesis of the eleutherobin core has been obtained. Both s...
Eleutherobin is a cytotoxic agent with microtubule stabilizing properties. A formal total synthesis...
This dissertation describes efforts towards synthesizing the BC ring system of eleutherobin, 1, a ma...
Asymmetric oxyallylation reactions and ring-closing metathesis have been used to synthesize compound...
The key step in a formal total synthesis of eleutherobin was an unprecedented kinetically controlled...
A short and efficient RCM route is reported for the construction of the key nine-membered B ring of ...
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...
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...
A practical synthesis of fully functionalized 'C' ring equivalent of cytotoxic marine natural produc...
The enantioselective synthesis of a number of simplified analogues of the cytotoxic natural product ...
The intramolecular Diels-Alder reaction is widely recognized as a powerful and versatile method for ...
Eleutherobin and dictyostatin are antimitotic compounds which exert their cytotoxic activity by a ta...
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcod...
An attractive intermediate in the total synthesis of the eleutherobin core has been obtained. Both s...
Eleutherobin is a cytotoxic agent with microtubule stabilizing properties. A formal total synthesis...
This dissertation describes efforts towards synthesizing the BC ring system of eleutherobin, 1, a ma...
Asymmetric oxyallylation reactions and ring-closing metathesis have been used to synthesize compound...
The key step in a formal total synthesis of eleutherobin was an unprecedented kinetically controlled...
A short and efficient RCM route is reported for the construction of the key nine-membered B ring of ...
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...
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...
A practical synthesis of fully functionalized 'C' ring equivalent of cytotoxic marine natural produc...
The enantioselective synthesis of a number of simplified analogues of the cytotoxic natural product ...
The intramolecular Diels-Alder reaction is widely recognized as a powerful and versatile method for ...
Eleutherobin and dictyostatin are antimitotic compounds which exert their cytotoxic activity by a ta...
An approach to the construction of A/B ring analogue of antitumour compounds eleutherobin and sarcod...
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