Total asymmetric synthesis of sperabillins B and D.
A concise route to the core fragment of sperabillins B and D, methyl (3R,5R,6R)-3,6-diamino-5-hydroxyheptanoate, has been developed with a subsequent novel protection strategy allowing the total asymmetric synthesis of sperabillins B and D.
Główni autorzy: | Davies, S, Kelly, R, Mortimer, A |
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Format: | Journal article |
Język: | English |
Wydane: |
2003
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