Regioselective Enzymatic Acylation of Multi-hydroxyl Compounds in Organic Synthesis
With current developments in enzyme-catalyzed reactions and techniques available for rational redesign of natural biocatalysts, the enzymatic biosynthesis can become one of the most valuable Synthetic methods. Enzymatic regioselective catalysis in organic media has played a key role in pursuing asym...
Saved in:
Published in | Biotechnology and bioprocess engineering Vol. 8; no. 1; pp. 1 - 8 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | Korean |
Published |
한국생물공학회
01.02.2003
|
Subjects | |
Online Access | Get full text |
ISSN | 1226-8372 1976-3816 |
Cover
Abstract | With current developments in enzyme-catalyzed reactions and techniques available for rational redesign of natural biocatalysts, the enzymatic biosynthesis can become one of the most valuable Synthetic methods. Enzymatic regioselective catalysis in organic media has played a key role in pursuing asymmetric synthesis for active chiral compounds. Here, we shortly do-scribe some historical issues of the rapidly growing area, enzymatic catalysis in synthetic organic chemistry and then review researches that have been carried out in the regioselective enzymatic catalysis for the past two decades. An application of this technology to the modification of some potential target drug co m pound will be adios presented. |
---|---|
AbstractList | With current developments in enzyme-catalyzed reactions and techniques available for rational redesign of natural biocatalysts, the enzymatic biosynthesis can become one of the most valuable Synthetic methods. Enzymatic regioselective catalysis in organic media has played a key role in pursuing asymmetric synthesis for active chiral compounds. Here, we shortly do-scribe some historical issues of the rapidly growing area, enzymatic catalysis in synthetic organic chemistry and then review researches that have been carried out in the regioselective enzymatic catalysis for the past two decades. An application of this technology to the modification of some potential target drug co m pound will be adios presented. With current developments in enzyme-catalyzed reactions and techniques available forrational redesign of natural biocatalysts, the enzymatic biosynthesis can become one of the most valuable synthetic methods. Enzymatic regioselective catalysis in organic media has played a key role in pursuing asymmetric synthesis for active chiral compounds. Here, we shortly describe some historical issues of the rapidly growing area, enzymatic catalysis in synthetic organic chemistry and then review researches that have been carried out in the regioselective enzymatic catalysis for the past two decades. An application of this technology to the modification of some potential target drug compound will be also presented. KCI Citation Count: 44 |
Author | Do, Jin-Hwan Chang, Ho-Nam Park, Hyun-Gyu |
Author_xml | – sequence: 1 fullname: Park, Hyun-Gyu – sequence: 2 fullname: Do, Jin-Hwan – sequence: 3 fullname: Chang, Ho-Nam |
BackLink | https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART000888950$$DAccess content in National Research Foundation of Korea (NRF) |
BookMark | eNotjstqwzAUREVJoUnaf9Cm0I3BeliSlyakz5RAkr1QrKtEtSMVyyl1v76m6WrO4swwMzQJMcAVmpJSiowpIiYjUyoyxSS9QbOUPvKcS6XUFG03cPAxQQt1778AL8PPcDK9r3FVD-0IMeDo8Pu57X12HGwXv4cWL-LpM56DTdgHvO4OJoyF7RD6IySfbtG1M22Cu_-co93jcrd4zlbrp5dFtcoawUQmOEgrbUEtQOFUARKoK4niipdgpbKMF8K5PSG85A7Gv0ZYQowzNbj9XrE5erjMhs7ppvY6Gv-Xh6ibTleb3YsmUkouRvX-ojY-9V6Px1v9Wr2taZ4zQkpKCkkIkewXBQFc7A |
ContentType | Journal Article |
DBID | JDI ACYCR |
DEWEY | 660.6 |
DatabaseName | KoreaScience Korean Citation Index |
DatabaseTitleList | |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Engineering |
DocumentTitleAlternate | Regioselective Enzymatic Acylation of Multi-hydroxyl Compounds in Organic Synthesis |
EISSN | 1976-3816 |
EndPage | 8 |
ExternalDocumentID | oai_kci_go_kr_ARTI_177746 JAKO200311921571117 |
GroupedDBID | --- -4Y -58 -5G -BR -EM -Y2 -~C .86 .UV .VR 06C 06D 0R~ 0VY 1N0 203 23N 2J2 2JN 2JY 2KG 2KM 2LR 2VQ 2WC 2~H 30V 3V. 4.4 406 408 40D 40E 53G 5GY 5VS 6NX 7WY 7X7 85H 88A 88I 8AO 8FE 8FG 8FH 8FI 8FJ 8FL 8UJ 95- 95. 95~ 96X 9ZL A8Z AAAVM AABHQ AABYN AAFGU AAGCJ AAHNG AAIAL AAIKT AAJKR AANZL AARHV AARTL AATNV AATVU AAUCO AAUYE AAWCG AAYFA AAYIU AAYQN AAYTO ABDZT ABECU ABFGW ABFTV ABHQN ABJCF ABJNI ABJOX ABKAS ABKCH ABMNI ABMQK ABNWP ABQBU ABSXP ABTEG ABTHY ABTKH ABTMW ABUWG ABWNU ABXPI ACBMV ACBRV ACBXY ACBYP ACGFS ACGOD ACHSB ACHXU ACIGE ACIPQ ACIWK ACKNC ACMDZ ACMLO ACOKC ACOMO ACPRK ACSNA ACTTH ACVWB ACWMK ADBBV ADHHG ADHIR ADINQ ADKNI ADKPE ADMDM ADOXG ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEEQQ AEFTE AEGAL AEGNC AEJHL AEJRE AEKMD AENEX AEOHA AEPYU AESKC AESTI AETLH AEVLU AEVTX AEXYK AFGCZ AFKRA AFLOW AFNRJ AFQWF AFRAH AFWTZ AFZKB AGAYW AGDGC AGGBP AGGDS AGJBK AGMZJ AGQMX AGWIL AGWZB AGYKE AHAVH AHBYD AHKAY AHMBA AHSBF AHYZX AIAKS AIIXL AILAN AIMYW AITGF AJBLW AJDOV AJGSW AJRNO AJZVZ AKQUC ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AMYQR AOCGG ARAPS ARCSS ARMRJ ASPBG AVWKF AXYYD AYJHY AZFZN AZQEC B-. BA0 BBNVY BBWZM BDATZ BENPR BEZIV BGLVJ BGNMA BHPHI BPHCQ BVXVI CAG CCPQU COF CS3 CSCUP DDRTE DNIVK DPUIP DU5 DWQXO E3Z EBD EBLON EBS EIOEI EJD ESBYG ESTFP FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRNLG FRRFC FSGXE FWDCC FYUFA G-Y G-Z GGCAI GGRSB GJIRD GNUQQ GNWQR GQ6 GQ7 GROUPED_ABI_INFORM_COMPLETE HCIFZ HF~ HG6 HMCUK HMJXF HRMNR HVGLF HZ~ I-F IJ- IKXTQ IWAJR IXC IXD I~X I~Z J-C J0Z JBSCW JDI JZLTJ K60 K6~ KOV KVFHK L6V LK8 LLZTM M0C M0L M2P M4Y M7P M7S MA- ML0 MZR N2Q NDZJH NF0 NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OK1 P19 P2P P62 P9N PF0 PQBIZ PQQKQ PROAC PT4 PT5 PTHSS Q2X QOK QOR QOS R89 R9I RHV RNI RNS ROL RPX RSV RZK S16 S1Z S26 S27 S28 S3B SAP SCG SCLPG SCM SDH SHX SISQX SNE SNPRN SNX SOHCF SOJ SPISZ SQXTU SRMVM SSLCW STPWE SZN T13 T16 TSG TUC TUS U2A UG4 UKHRP UNUBA UOJIU UTJUX UZXMN VC2 VFIZW W48 W4F WK8 YLTOR Z45 Z5O Z7U Z7V Z7W Z8Q ZMTXR ZZE ~A9 AAPBV ACYCR |
ID | FETCH-LOGICAL-k636-64e7d7d52dee5f85e7e2f9184849ed78d3456ffb11494fe478a6d11afacefbb83 |
ISSN | 1226-8372 |
IngestDate | Tue Nov 21 21:26:24 EST 2023 Fri Dec 22 11:59:14 EST 2023 |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Keywords | regioselective synthesis drug modification enzymatic synthesis Sugar acylation glycoside jineol |
Language | Korean |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-k636-64e7d7d52dee5f85e7e2f9184849ed78d3456ffb11494fe478a6d11afacefbb83 |
Notes | KISTI1.1003/JNL.JAKO200311921571117 G704-000785.2003.8.1.007 |
OpenAccessLink | http://click.ndsl.kr/servlet/LinkingDetailView?cn=JAKO200311921571117&dbt=JAKO&org_code=O481&site_code=SS1481&service_code=01 |
PageCount | 8 |
ParticipantIDs | nrf_kci_oai_kci_go_kr_ARTI_177746 kisti_ndsl_JAKO200311921571117 |
PublicationCentury | 2000 |
PublicationDate | 2003-02 |
PublicationDateYYYYMMDD | 2003-02-01 |
PublicationDate_xml | – month: 02 year: 2003 text: 2003-02 |
PublicationDecade | 2000 |
PublicationTitle | Biotechnology and bioprocess engineering |
PublicationTitleAlternate | Biotechnology and bioprocess engineering : Bbe |
PublicationYear | 2003 |
Publisher | 한국생물공학회 |
Publisher_xml | – name: 한국생물공학회 |
SSID | ssj0047888 ssib004208035 ssib053376792 |
Score | 1.5741229 |
Snippet | With current developments in enzyme-catalyzed reactions and techniques available for rational redesign of natural biocatalysts, the enzymatic biosynthesis can... With current developments in enzyme-catalyzed reactions and techniques available forrational redesign of natural biocatalysts, the enzymatic biosynthesis can... |
SourceID | nrf kisti |
SourceType | Open Website Open Access Repository |
StartPage | 1 |
SubjectTerms | 생물공학 |
Title | Regioselective Enzymatic Acylation of Multi-hydroxyl Compounds in Organic Synthesis |
URI | http://click.ndsl.kr/servlet/LinkingDetailView?cn=JAKO200311921571117&dbt=JAKO&org_code=O481&site_code=SS1481&service_code=01 https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART000888950 |
Volume | 8 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
ispartofPNX | Biotechnology and Bioprocess Engineering, 2003, 8(1), , pp.1-8 |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9QwGLVoucChallEC62MxK0yaiaJnRynVdtQxCDRQeot8tpGMyRoFqH01_PZnnEyUInlkox8iDJ-zvP7_G0IvYtFNNA2MxfUCCOJToAHmVREK6NTyRORuWI6n0a0-Jpc3aQ3XbdNl12yEO_l_YN5Jf-DKowBrjZL9h-QDQ-FAfgN-MIVEIbrX2H8Rd9Wzdx1srEBQOf1fesrsA5lOw1a0OXYkrtW2YiVqWMA20vJBcL6VEx5fN3WoATn1XzDyVs1i3Dy7rwMomq--8yCY90VMuzcUD7uumiXNblsl0Eke-9OVZPiR7cYz9ZH1UVDRvzbxvFDvI5YDowJ-o2AlespVfsx0DjEeiT7NJv9tpo8ZUb9vbfbldae-F82qxBCeDX8-Nm-T2QLuqUMKJttoa04Aq57PLw4PR31WAnWYScKQd8yyvJQZMz2D3AJk-s_AmaK1e4VqI16ZnpqY7yLdlZmAh56zPfQo0nzDD3tFY98jq430ccBfRzQx43Bm-jjgD6uarxCHwf0X6Dxxfn4rCCrFhlkQmNKaKKZYiodKK1Tk6Wa6YHJwWjPklwrlqkY9LExAozePDHwIWacqijihkttBHyHL9F23dT6FcKcZ4rmIOdB0iaZjHlk5AnjlEkxUOZE7KMjNyslvOG0fGD299FbmK5yIqvSliy399umnMxKMMw-lBEDO4Me_Okhr9GTbpG9QduL2VIfgupbiKMVrD8BAmtZog |
linkProvider | Library Specific Holdings |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Regioselective+Enzymatic+Acylation+of+Multi-hydroxyl+Compounds+in+Organic+Synthesis&rft.jtitle=Biotechnology+and+bioprocess+engineering&rft.au=Park%2C+Hyun-Gyu&rft.au=Do%2C+Jin-Hwan&rft.au=Chang%2C+Ho-Nam&rft.date=2003-02-01&rft.issn=1226-8372&rft.eissn=1976-3816&rft.volume=8&rft.issue=1&rft.spage=1&rft.epage=8&rft.externalDBID=n%2Fa&rft.externalDocID=JAKO200311921571117 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1226-8372&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1226-8372&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1226-8372&client=summon |