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Chem Commun (Camb) ; (20): 2616-7, 2003 Oct 21.
Article in English | MEDLINE | ID: mdl-14594308

ABSTRACT

The relative and absolute stereochemistry of amphidinoketide I has been determined by the total synthesis of all the diastereoisomers. Molecular modelling suggests that the natural product is not the thermodynamically preferred diastereoisomer.


Subject(s)
Macrolides/chemistry , Animals , Dinoflagellida/chemistry , Macrolides/chemical synthesis , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Stereoisomerism
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