A chemoenzymatic total synthesis of ent-bengamide E

M. G. Banwell; K. J. McRae

doi:10.1021/jo0159486

A chemoenzymatic total synthesis of ent-bengamide E

M. G. Banwell^*, K. J. McRae

^*Corresponding author for this work

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

41 Citations (Scopus)

Abstract

The cis-1,2-dihydrocatechol 3, which can be obtained in enantiomerically pure form by microbial dihydroxylation of bromobenzene, has been converted into the enantiomer, ent-1, of the cyclolysine-based marine natural product bengamide E (1).

Original language	English
Pages (from-to)	6768-6774
Number of pages	7
Journal	Journal of Organic Chemistry
Volume	66
Issue number	20
DOIs	https://doi.org/10.1021/jo0159486
Publication status	Published - 5 Oct 2001

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title = "A chemoenzymatic total synthesis of ent-bengamide E",

abstract = "The cis-1,2-dihydrocatechol 3, which can be obtained in enantiomerically pure form by microbial dihydroxylation of bromobenzene, has been converted into the enantiomer, ent-1, of the cyclolysine-based marine natural product bengamide E (1).",

author = "Banwell, \{M. G.\} and McRae, \{K. J.\}",

year = "2001",

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AU - McRae, K. J.

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N2 - The cis-1,2-dihydrocatechol 3, which can be obtained in enantiomerically pure form by microbial dihydroxylation of bromobenzene, has been converted into the enantiomer, ent-1, of the cyclolysine-based marine natural product bengamide E (1).

AB - The cis-1,2-dihydrocatechol 3, which can be obtained in enantiomerically pure form by microbial dihydroxylation of bromobenzene, has been converted into the enantiomer, ent-1, of the cyclolysine-based marine natural product bengamide E (1).

UR - https://www.scopus.com/pages/publications/0035812744

U2 - 10.1021/jo0159486

DO - 10.1021/jo0159486

M3 - Article

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EP - 6774

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 20

ER -

A chemoenzymatic total synthesis of ent-bengamide E

Abstract

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