Chemoenzymatic synthesis of (+)-aspicilin from chlorobenzene

Martin G. Banwell; Kenneth J. McRae

doi:10.1021/ol006457v

Chemoenzymatic synthesis of (+)-aspicilin from chlorobenzene

Martin G. Banwell^*, Kenneth J. McRae

^*Corresponding author for this work

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

38 Citations (Scopus)

Abstract

(matrix presented) The enantiomerically pure cis-1,2-dihydrocatechol 2, which is obtained by microbial oxidation of chlorobenzene, has been converted, via intermediate 3, into the natural product (+)-aspicilin (1).

Original language	English
Pages (from-to)	3583-3586
Number of pages	4
Journal	Organic Letters
Volume	2
Issue number	23
DOIs	https://doi.org/10.1021/ol006457v
Publication status	Published - 16 Nov 2000

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title = "Chemoenzymatic synthesis of (+)-aspicilin from chlorobenzene",

abstract = "(matrix presented) The enantiomerically pure cis-1,2-dihydrocatechol 2, which is obtained by microbial oxidation of chlorobenzene, has been converted, via intermediate 3, into the natural product (+)-aspicilin (1).",

author = "Banwell, {Martin G.} and McRae, {Kenneth J.}",

year = "2000",

month = nov,

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doi = "10.1021/ol006457v",

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journal = "Organic Letters",

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T1 - Chemoenzymatic synthesis of (+)-aspicilin from chlorobenzene

AU - Banwell, Martin G.

AU - McRae, Kenneth J.

PY - 2000/11/16

Y1 - 2000/11/16

N2 - (matrix presented) The enantiomerically pure cis-1,2-dihydrocatechol 2, which is obtained by microbial oxidation of chlorobenzene, has been converted, via intermediate 3, into the natural product (+)-aspicilin (1).

AB - (matrix presented) The enantiomerically pure cis-1,2-dihydrocatechol 2, which is obtained by microbial oxidation of chlorobenzene, has been converted, via intermediate 3, into the natural product (+)-aspicilin (1).

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U2 - 10.1021/ol006457v

DO - 10.1021/ol006457v

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VL - 2

SP - 3583

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JO - Organic Letters

JF - Organic Letters

IS - 23

ER -

Chemoenzymatic synthesis of (+)-aspicilin from chlorobenzene

Abstract

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