Chemoenzymatic total synthesis and reassignment of the absolute configuration of ribisin C

Ping Lan; Martin G. Banwell; Jas S. Ward; Anthony C. Willis

doi:10.1021/ol403220t

Chemoenzymatic total synthesis and reassignment of the absolute configuration of ribisin C

Ping Lan, Martin G. Banwell^*, Jas S. Ward, Anthony C. Willis

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

17 Citations (Scopus)

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.

Original language	English
Pages (from-to)	228-231
Number of pages	4
Journal	Organic Letters
Volume	16
Issue number	1
DOIs	https://doi.org/10.1021/ol403220t
Publication status	Published - 3 Jan 2014

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10.1021/ol403220t

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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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AU - Ward, Jas S.

AU - Willis, Anthony C.

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AB - 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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JO - Organic Letters

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IS - 1

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Chemoenzymatic total synthesis and reassignment of the absolute configuration of ribisin C

Abstract

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