A Facile Stereoselective Biocatalytic Route to the Precursor of Woody Acetate
Carbonyl reductase (CRED) technology has been shown to be an important tool for the rapid and efficient preparation of cis- and trans-4-tert-butylcyclohexanol, the precursors to the high volume fragrance ingredients known as Woody Acetate.
Gespeichert in:
Veröffentlicht in: | Organic process research & development 2011-09, Vol.15 (5), p.1036-1039 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1039 |
---|---|
container_issue | 5 |
container_start_page | 1036 |
container_title | Organic process research & development |
container_volume | 15 |
creator | Brown, Gareth Mangan, David Miskelly, Iain Moody, Thomas S |
description | Carbonyl reductase (CRED) technology has been shown to be an important tool for the rapid and efficient preparation of cis- and trans-4-tert-butylcyclohexanol, the precursors to the high volume fragrance ingredients known as Woody Acetate. |
doi_str_mv | 10.1021/op200166a |
format | Article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_op200166a</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>h15845629</sourcerecordid><originalsourceid>FETCH-LOGICAL-a325t-ececed384b9b1e79fbe4a5b73d3e0e627ce53a8ffc0f659c0baffd6c40a6575f3</originalsourceid><addsrcrecordid>eNptkE9LAzEUxIMoWKsHv0EuHjysvmya7Pa4FqtCRfEPelvevn3BLaspSVrot3el4knmMHP4MQwjxKmCCwW5uvSrHEBZi3tipEwOmSnt-_6QodSZVRYOxVGMSwAwVuUjcV_JOVLXs3xOHNhH7plSt2F51XnChP02dSSf_DqxTF6mD5aPgWkdog_SO_nmfbuVFXHCxMfiwGEf-eTXx-J1fv0yu80WDzd3s2qRoc5NypgGtbqcNNNGcTF1DU_QNIVuNQPbvCA2GkvnCJw1U4IGnWstTQCtKYzTY3G-66XgYwzs6lXoPjFsawX1zw_13w8De7ZjkWK99OvwNSz7h_sGeTFd4A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>A Facile Stereoselective Biocatalytic Route to the Precursor of Woody Acetate</title><source>American Chemical Society Journals</source><creator>Brown, Gareth ; Mangan, David ; Miskelly, Iain ; Moody, Thomas S</creator><creatorcontrib>Brown, Gareth ; Mangan, David ; Miskelly, Iain ; Moody, Thomas S</creatorcontrib><description>Carbonyl reductase (CRED) technology has been shown to be an important tool for the rapid and efficient preparation of cis- and trans-4-tert-butylcyclohexanol, the precursors to the high volume fragrance ingredients known as Woody Acetate.</description><identifier>ISSN: 1083-6160</identifier><identifier>EISSN: 1520-586X</identifier><identifier>DOI: 10.1021/op200166a</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Organic process research & development, 2011-09, Vol.15 (5), p.1036-1039</ispartof><rights>Copyright © 2011 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a325t-ececed384b9b1e79fbe4a5b73d3e0e627ce53a8ffc0f659c0baffd6c40a6575f3</citedby><cites>FETCH-LOGICAL-a325t-ececed384b9b1e79fbe4a5b73d3e0e627ce53a8ffc0f659c0baffd6c40a6575f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/op200166a$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/op200166a$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27081,27929,27930,56743,56793</link.rule.ids></links><search><creatorcontrib>Brown, Gareth</creatorcontrib><creatorcontrib>Mangan, David</creatorcontrib><creatorcontrib>Miskelly, Iain</creatorcontrib><creatorcontrib>Moody, Thomas S</creatorcontrib><title>A Facile Stereoselective Biocatalytic Route to the Precursor of Woody Acetate</title><title>Organic process research & development</title><addtitle>Org. Process Res. Dev</addtitle><description>Carbonyl reductase (CRED) technology has been shown to be an important tool for the rapid and efficient preparation of cis- and trans-4-tert-butylcyclohexanol, the precursors to the high volume fragrance ingredients known as Woody Acetate.</description><issn>1083-6160</issn><issn>1520-586X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNptkE9LAzEUxIMoWKsHv0EuHjysvmya7Pa4FqtCRfEPelvevn3BLaspSVrot3el4knmMHP4MQwjxKmCCwW5uvSrHEBZi3tipEwOmSnt-_6QodSZVRYOxVGMSwAwVuUjcV_JOVLXs3xOHNhH7plSt2F51XnChP02dSSf_DqxTF6mD5aPgWkdog_SO_nmfbuVFXHCxMfiwGEf-eTXx-J1fv0yu80WDzd3s2qRoc5NypgGtbqcNNNGcTF1DU_QNIVuNQPbvCA2GkvnCJw1U4IGnWstTQCtKYzTY3G-66XgYwzs6lXoPjFsawX1zw_13w8De7ZjkWK99OvwNSz7h_sGeTFd4A</recordid><startdate>20110916</startdate><enddate>20110916</enddate><creator>Brown, Gareth</creator><creator>Mangan, David</creator><creator>Miskelly, Iain</creator><creator>Moody, Thomas S</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20110916</creationdate><title>A Facile Stereoselective Biocatalytic Route to the Precursor of Woody Acetate</title><author>Brown, Gareth ; Mangan, David ; Miskelly, Iain ; Moody, Thomas S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a325t-ececed384b9b1e79fbe4a5b73d3e0e627ce53a8ffc0f659c0baffd6c40a6575f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brown, Gareth</creatorcontrib><creatorcontrib>Mangan, David</creatorcontrib><creatorcontrib>Miskelly, Iain</creatorcontrib><creatorcontrib>Moody, Thomas S</creatorcontrib><collection>CrossRef</collection><jtitle>Organic process research & development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brown, Gareth</au><au>Mangan, David</au><au>Miskelly, Iain</au><au>Moody, Thomas S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Facile Stereoselective Biocatalytic Route to the Precursor of Woody Acetate</atitle><jtitle>Organic process research & development</jtitle><addtitle>Org. Process Res. Dev</addtitle><date>2011-09-16</date><risdate>2011</risdate><volume>15</volume><issue>5</issue><spage>1036</spage><epage>1039</epage><pages>1036-1039</pages><issn>1083-6160</issn><eissn>1520-586X</eissn><abstract>Carbonyl reductase (CRED) technology has been shown to be an important tool for the rapid and efficient preparation of cis- and trans-4-tert-butylcyclohexanol, the precursors to the high volume fragrance ingredients known as Woody Acetate.</abstract><pub>American Chemical Society</pub><doi>10.1021/op200166a</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1083-6160 |
ispartof | Organic process research & development, 2011-09, Vol.15 (5), p.1036-1039 |
issn | 1083-6160 1520-586X |
language | eng |
recordid | cdi_crossref_primary_10_1021_op200166a |
source | American Chemical Society Journals |
title | A Facile Stereoselective Biocatalytic Route to the Precursor of Woody Acetate |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T03%3A26%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Facile%20Stereoselective%20Biocatalytic%20Route%20to%20the%20Precursor%20of%20Woody%20Acetate&rft.jtitle=Organic%20process%20research%20&%20development&rft.au=Brown,%20Gareth&rft.date=2011-09-16&rft.volume=15&rft.issue=5&rft.spage=1036&rft.epage=1039&rft.pages=1036-1039&rft.issn=1083-6160&rft.eissn=1520-586X&rft_id=info:doi/10.1021/op200166a&rft_dat=%3Cacs_cross%3Eh15845629%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |