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

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

24 Citations (SciVal)

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

Access to Document

10.1071/CH09469

Cite this

@article{8cd5e4496b0a408da1670050e660df12,

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.",

author = "Pinkerton, {David M.} and Banwell, {Martin G.} and Willis, {Anthony C.}",

year = "2009",

doi = "10.1071/CH09469",

language = "English",

volume = "62",

pages = "1639--1645",

journal = "Australian Journal of Chemistry",

issn = "0004-9425",

publisher = "CSIRO",

number = "12",

}

TY - JOUR

T1 - Rapid, chemoenzymatic syntheses of the epoxyquinols ()-bromoxone acetate and ()-tricholomenyn A

AU - Pinkerton, David M.

AU - Banwell, Martin G.

AU - Willis, Anthony C.

PY - 2009

Y1 - 2009

N2 - 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.

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.

UR - http://www.scopus.com/inward/record.url?scp=76849105736&partnerID=8YFLogxK

U2 - 10.1071/CH09469

DO - 10.1071/CH09469

M3 - Article

SN - 0004-9425

VL - 62

SP - 1639

EP - 1645

JO - Australian Journal of Chemistry

JF - Australian Journal of Chemistry

IS - 12

ER -

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

Abstract

Access to Document

Other files and links

Fingerprint

Cite this