Rapid, chemoenzymatic syntheses of the epoxyquinols ()-bromoxone acetate and ()-tricholomenyn A

David M. Pinkerton; Martin G. Banwell; Anthony C. Willis

doi:10.1071/CH09469

Rapid, chemoenzymatic syntheses of the epoxyquinols ()-bromoxone acetate and ()-tricholomenyn A

David M. Pinkerton, Martin G. Banwell, Anthony C. Willis

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22 Citations (Scopus)

Abstract

The epoxyquinol derivatives (-)-bromoxone acetate (ent-1) and (-)-tricholomenyn A (2) have been prepared from the cis-1,2-dihydrocatechols 3 and 4, respectively. Compounds 3 and 4 are themselves obtained in enantiomerically pure form through the whole-cell biotransformation of the corresponding halobenzene.

Original language	English
Pages (from-to)	1639-1645
Number of pages	7
Journal	Australian Journal of Chemistry
Volume	62
Issue number	12
DOIs	https://doi.org/10.1071/CH09469
Publication status	Published - 2009

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title = "Rapid, chemoenzymatic syntheses of the epoxyquinols ()-bromoxone acetate and ()-tricholomenyn A",

abstract = "The epoxyquinol derivatives (-)-bromoxone acetate (ent-1) and (-)-tricholomenyn A (2) have been prepared from the cis-1,2-dihydrocatechols 3 and 4, respectively. Compounds 3 and 4 are themselves obtained in enantiomerically pure form through the whole-cell biotransformation of the corresponding halobenzene.",

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AU - Banwell, Martin G.

AU - Willis, Anthony C.

PY - 2009

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AB - The epoxyquinol derivatives (-)-bromoxone acetate (ent-1) and (-)-tricholomenyn A (2) have been prepared from the cis-1,2-dihydrocatechols 3 and 4, respectively. Compounds 3 and 4 are themselves obtained in enantiomerically pure form through the whole-cell biotransformation of the corresponding halobenzene.

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JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

IS - 12

ER -

Rapid, chemoenzymatic syntheses of the epoxyquinols ()-bromoxone acetate and ()-tricholomenyn A

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