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Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
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Chemoenzymatic total synthesis and reassignment of the absolute configuration of ribisin C
Ping Lan1, Martin G Banwell, Jas S Ward
1Research School of Chemistry, Institute of Advanced Studies, The Australian National University , Canberra ACT 0200, Australia.
Organic Letters
|December 17, 2013
Abstract:
The enantiomerically pure and enzymatically derived cis-1,2-dihydrocatechol 5 has been converted, by two related pathways, into compounds 3 and ent-3. As a result, it has been determined that the true structure of the natural product ribisin C is represented by ent-3.
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