Synthesis of simplified analogues of eleutherobin via a Claisen rearrangement/RCM strategy
The enantioselective synthesis of a number of simplified analogues of the cytotoxic natural product eleutherobin is reported. © 2009 Elsevier Ltd. All rights reserved.
Κύριοι συγγραφείς: | Mak, S, Chiang, G, Davidson, J, Davies, J, Ayscough, A, Pain, G, Burton, J, Holmes, AB |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2009
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Synthesis and biological evaluation of eleutherobin analgoues
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The Claisen rearrangement approach to fused bicyclic medium-ring oxacycles.
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Synthesis of fused bicyclic medium-ring lactones via Claisen rearrangement
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Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
ανά: Anderson, E, κ.ά.
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Synthesis of C ring of Eleutherobin
ανά: S. Chandrasekhar, κ.ά.
Έκδοση: (2004-11-01)