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.

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Hlavní autoři: Davies, S, Kelly, R, Mortimer, A
Médium: Journal article
Jazyk:English
Vydáno: 2003