Chemoenzymatic and microbial dynamic kinetic resolutions

This review tracks a decade of dynamic kinetic resolution developments with a biocatalytic inclination using enzymatic/microbial means for the resolution part followed by the racemization reactions either by means of enzymatic or chemocatalyst. These fast developments are due to the ability of the b...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Chirality (New York, N.Y.) N.Y.), 2009-04, Vol.21 (4), p.449-467
Hauptverfasser: Kamaruddin, Azlina Harun, Uzir, Mohamad Hekarl, Aboul-Enein, Hassan Y., Halim, Hairul Nazirah Abdul
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 467
container_issue 4
container_start_page 449
container_title Chirality (New York, N.Y.)
container_volume 21
creator Kamaruddin, Azlina Harun
Uzir, Mohamad Hekarl
Aboul-Enein, Hassan Y.
Halim, Hairul Nazirah Abdul
description This review tracks a decade of dynamic kinetic resolution developments with a biocatalytic inclination using enzymatic/microbial means for the resolution part followed by the racemization reactions either by means of enzymatic or chemocatalyst. These fast developments are due to the ability of the biocatalysts to significantly reduce the number of synthetic steps which are common for conventional synthesis. Future developments in novel reactions and products of dynamic kinetic resolutions should consider factors that are needed to be extracted at the early synthetic stage to avoid inhibition at scale‐up stage have been highlighted. Chirality, 2009. © 2008 Wiley‐Liss, Inc.
doi_str_mv 10.1002/chir.20619
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67055260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20476328</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4629-5f67117e40a21f9713b70b7d05918e76007d3965138959232134236960cb43c53</originalsourceid><addsrcrecordid>eNqFkMtOwzAQRS0EoqWw4QNQVyyQUsZ2bMdLqOhDVEXivbOcxFVN8yh2IihfT0oL7GA1Gs25V5qD0DGGHgYg58ncuh4BjuUOamNGIOCUP--iNkRSBgAhaaED718AQHIa7qMWjjhjOII2ivpzk5em-FjlurJJVxdpN7eJK2Ors266KnSzdRe2MOurM77M6sqWhT9EezOdeXO0nR30MLi674-Cyc1w3L-YBEnIiQzYjAuMhQlBEzyTAtNYQCxSYBJHRnAAkVLJGaaRZJJQgmlIKJcckjikCaMddLrpXbrytTa-Urn1ickyXZiy9ooLYIxw-BckEApOSdSAZxuw-dJ7Z2Zq6Wyu3UphUGuhai1UfQlt4JNtax3nJv1FtwYbAG-AN5uZ1R9Vqj8a336XBpuM9ZV5_8lot2jeoYKpp-lQDS5hCtePd2pEPwFZi40B</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20476328</pqid></control><display><type>article</type><title>Chemoenzymatic and microbial dynamic kinetic resolutions</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Kamaruddin, Azlina Harun ; Uzir, Mohamad Hekarl ; Aboul-Enein, Hassan Y. ; Halim, Hairul Nazirah Abdul</creator><creatorcontrib>Kamaruddin, Azlina Harun ; Uzir, Mohamad Hekarl ; Aboul-Enein, Hassan Y. ; Halim, Hairul Nazirah Abdul</creatorcontrib><description>This review tracks a decade of dynamic kinetic resolution developments with a biocatalytic inclination using enzymatic/microbial means for the resolution part followed by the racemization reactions either by means of enzymatic or chemocatalyst. These fast developments are due to the ability of the biocatalysts to significantly reduce the number of synthetic steps which are common for conventional synthesis. Future developments in novel reactions and products of dynamic kinetic resolutions should consider factors that are needed to be extracted at the early synthetic stage to avoid inhibition at scale‐up stage have been highlighted. Chirality, 2009. © 2008 Wiley‐Liss, Inc.</description><identifier>ISSN: 0899-0042</identifier><identifier>EISSN: 1520-636X</identifier><identifier>DOI: 10.1002/chir.20619</identifier><identifier>PMID: 18655180</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Alcohols - chemistry ; biocatalysts ; Carboxylic Acids - chemistry ; Catalysis ; Chemistry, Organic - methods ; chemocatalysts ; chiral resoluion ; dynamic kinetic resolution ; Enzymes - chemistry ; Esterification ; Esters - chemistry ; Fenoprofen - chemistry ; Fungal Proteins - chemistry ; Hydrolysis ; Ibuprofen - chemistry ; Kinetics ; Molecular Structure ; Naproxen - chemistry ; Stereoisomerism ; Suprofen - chemistry</subject><ispartof>Chirality (New York, N.Y.), 2009-04, Vol.21 (4), p.449-467</ispartof><rights>Copyright © 2008 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4629-5f67117e40a21f9713b70b7d05918e76007d3965138959232134236960cb43c53</citedby><cites>FETCH-LOGICAL-c4629-5f67117e40a21f9713b70b7d05918e76007d3965138959232134236960cb43c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchir.20619$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchir.20619$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18655180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kamaruddin, Azlina Harun</creatorcontrib><creatorcontrib>Uzir, Mohamad Hekarl</creatorcontrib><creatorcontrib>Aboul-Enein, Hassan Y.</creatorcontrib><creatorcontrib>Halim, Hairul Nazirah Abdul</creatorcontrib><title>Chemoenzymatic and microbial dynamic kinetic resolutions</title><title>Chirality (New York, N.Y.)</title><addtitle>Chirality</addtitle><description>This review tracks a decade of dynamic kinetic resolution developments with a biocatalytic inclination using enzymatic/microbial means for the resolution part followed by the racemization reactions either by means of enzymatic or chemocatalyst. These fast developments are due to the ability of the biocatalysts to significantly reduce the number of synthetic steps which are common for conventional synthesis. Future developments in novel reactions and products of dynamic kinetic resolutions should consider factors that are needed to be extracted at the early synthetic stage to avoid inhibition at scale‐up stage have been highlighted. Chirality, 2009. © 2008 Wiley‐Liss, Inc.</description><subject>Alcohols - chemistry</subject><subject>biocatalysts</subject><subject>Carboxylic Acids - chemistry</subject><subject>Catalysis</subject><subject>Chemistry, Organic - methods</subject><subject>chemocatalysts</subject><subject>chiral resoluion</subject><subject>dynamic kinetic resolution</subject><subject>Enzymes - chemistry</subject><subject>Esterification</subject><subject>Esters - chemistry</subject><subject>Fenoprofen - chemistry</subject><subject>Fungal Proteins - chemistry</subject><subject>Hydrolysis</subject><subject>Ibuprofen - chemistry</subject><subject>Kinetics</subject><subject>Molecular Structure</subject><subject>Naproxen - chemistry</subject><subject>Stereoisomerism</subject><subject>Suprofen - chemistry</subject><issn>0899-0042</issn><issn>1520-636X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqWw4QNQVyyQUsZ2bMdLqOhDVEXivbOcxFVN8yh2IihfT0oL7GA1Gs25V5qD0DGGHgYg58ncuh4BjuUOamNGIOCUP--iNkRSBgAhaaED718AQHIa7qMWjjhjOII2ivpzk5em-FjlurJJVxdpN7eJK2Ors266KnSzdRe2MOurM77M6sqWhT9EezOdeXO0nR30MLi674-Cyc1w3L-YBEnIiQzYjAuMhQlBEzyTAtNYQCxSYBJHRnAAkVLJGaaRZJJQgmlIKJcckjikCaMddLrpXbrytTa-Urn1ickyXZiy9ooLYIxw-BckEApOSdSAZxuw-dJ7Z2Zq6Wyu3UphUGuhai1UfQlt4JNtax3nJv1FtwYbAG-AN5uZ1R9Vqj8a336XBpuM9ZV5_8lot2jeoYKpp-lQDS5hCtePd2pEPwFZi40B</recordid><startdate>200904</startdate><enddate>200904</enddate><creator>Kamaruddin, Azlina Harun</creator><creator>Uzir, Mohamad Hekarl</creator><creator>Aboul-Enein, Hassan Y.</creator><creator>Halim, Hairul Nazirah Abdul</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200904</creationdate><title>Chemoenzymatic and microbial dynamic kinetic resolutions</title><author>Kamaruddin, Azlina Harun ; Uzir, Mohamad Hekarl ; Aboul-Enein, Hassan Y. ; Halim, Hairul Nazirah Abdul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4629-5f67117e40a21f9713b70b7d05918e76007d3965138959232134236960cb43c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Alcohols - chemistry</topic><topic>biocatalysts</topic><topic>Carboxylic Acids - chemistry</topic><topic>Catalysis</topic><topic>Chemistry, Organic - methods</topic><topic>chemocatalysts</topic><topic>chiral resoluion</topic><topic>dynamic kinetic resolution</topic><topic>Enzymes - chemistry</topic><topic>Esterification</topic><topic>Esters - chemistry</topic><topic>Fenoprofen - chemistry</topic><topic>Fungal Proteins - chemistry</topic><topic>Hydrolysis</topic><topic>Ibuprofen - chemistry</topic><topic>Kinetics</topic><topic>Molecular Structure</topic><topic>Naproxen - chemistry</topic><topic>Stereoisomerism</topic><topic>Suprofen - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kamaruddin, Azlina Harun</creatorcontrib><creatorcontrib>Uzir, Mohamad Hekarl</creatorcontrib><creatorcontrib>Aboul-Enein, Hassan Y.</creatorcontrib><creatorcontrib>Halim, Hairul Nazirah Abdul</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chirality (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kamaruddin, Azlina Harun</au><au>Uzir, Mohamad Hekarl</au><au>Aboul-Enein, Hassan Y.</au><au>Halim, Hairul Nazirah Abdul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemoenzymatic and microbial dynamic kinetic resolutions</atitle><jtitle>Chirality (New York, N.Y.)</jtitle><addtitle>Chirality</addtitle><date>2009-04</date><risdate>2009</risdate><volume>21</volume><issue>4</issue><spage>449</spage><epage>467</epage><pages>449-467</pages><issn>0899-0042</issn><eissn>1520-636X</eissn><abstract>This review tracks a decade of dynamic kinetic resolution developments with a biocatalytic inclination using enzymatic/microbial means for the resolution part followed by the racemization reactions either by means of enzymatic or chemocatalyst. These fast developments are due to the ability of the biocatalysts to significantly reduce the number of synthetic steps which are common for conventional synthesis. Future developments in novel reactions and products of dynamic kinetic resolutions should consider factors that are needed to be extracted at the early synthetic stage to avoid inhibition at scale‐up stage have been highlighted. Chirality, 2009. © 2008 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18655180</pmid><doi>10.1002/chir.20619</doi><tpages>19</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0899-0042
ispartof Chirality (New York, N.Y.), 2009-04, Vol.21 (4), p.449-467
issn 0899-0042
1520-636X
language eng
recordid cdi_proquest_miscellaneous_67055260
source MEDLINE; Wiley Online Library All Journals
subjects Alcohols - chemistry
biocatalysts
Carboxylic Acids - chemistry
Catalysis
Chemistry, Organic - methods
chemocatalysts
chiral resoluion
dynamic kinetic resolution
Enzymes - chemistry
Esterification
Esters - chemistry
Fenoprofen - chemistry
Fungal Proteins - chemistry
Hydrolysis
Ibuprofen - chemistry
Kinetics
Molecular Structure
Naproxen - chemistry
Stereoisomerism
Suprofen - chemistry
title Chemoenzymatic and microbial dynamic kinetic resolutions
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T15%3A16%3A30IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chemoenzymatic%20and%20microbial%20dynamic%20kinetic%20resolutions&rft.jtitle=Chirality%20(New%20York,%20N.Y.)&rft.au=Kamaruddin,%20Azlina%20Harun&rft.date=2009-04&rft.volume=21&rft.issue=4&rft.spage=449&rft.epage=467&rft.pages=449-467&rft.issn=0899-0042&rft.eissn=1520-636X&rft_id=info:doi/10.1002/chir.20619&rft_dat=%3Cproquest_cross%3E20476328%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=20476328&rft_id=info:pmid/18655180&rfr_iscdi=true