Stereospecific Synthesis of (−)-Neplanocin F
The stereospecific synthesis of (−)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an access through appropriate modifications to new series of carbanucleosides.
Saved in:
| Published in | Nucleosides, nucleotides & nucleic acids Vol. 26; no. 8-9; pp. 1111 - 1114 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Taylor & Francis Group
01.01.2007
|
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | The stereospecific synthesis of (−)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an access through appropriate modifications to new series of carbanucleosides. |
|---|---|
| AbstractList | The stereospecific synthesis of (−)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an access through appropriate modifications to new series of carbanucleosides. The stereospecific synthesis of (-)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an access through appropriate modifications to new series of carbanucleosides. |
| Author | Mathé, Christophe Périgaud, Christian Ropero, Sergio Rodriguez Edmont, Dolorès |
| Author_xml | – sequence: 1 givenname: Sergio Rodriguez surname: Ropero fullname: Ropero, Sergio Rodriguez organization: UMR 5625 CNRS-UM II, Université Montpellier II – sequence: 2 givenname: Dolorès surname: Edmont fullname: Edmont, Dolorès organization: UMR 5625 CNRS-UM II, Université Montpellier II – sequence: 3 givenname: Christophe surname: Mathé fullname: Mathé, Christophe organization: UMR 5625 CNRS-UM II, Université Montpellier II – sequence: 4 givenname: Christian surname: Périgaud fullname: Périgaud, Christian organization: UMR 5625 CNRS-UM II, Université Montpellier II |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18058547$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkMtKAzEYhYNU7EUfwI3MSnQxNZfJJANupFgVii6q65BmEozMTMZkivYNXPuIPokpLbgo0n9z_sV3DoczBL3GNRqAUwTHCHJ4hSimjDHIYPwQ5tkBGCBKcIoJob31j2m6BvpgGMIbhIhDzo5APyrlNGMDMJ532msXWq2ssSqZr5ruVQcbEmeSi5-v78v0UbeVbJyyTTI9BodGVkGfbHUEXqa3z5P7dPZ09zC5maUqI6hLSxnrSWxMKcu8UEjzhTGMaGWUzDgiRsWDKi9zCEvMOY1FlZaUK5IVTCsyAueb3Na796UOnahtULqKRbRbBpEXkBQMZntBjGAWt2IRRBtQeReC10a03tbSrwSCYr2m2Fkzes624ctFrcs_x3a-CLANYBvjfC0_nK9K0clV5bzxslE27MaK7rOLzuu9TvJ_s1-nU5Zy |
| CitedBy_id | crossref_primary_10_1002_chin_200812254 |
| Cites_doi | 10.1128/AAC.28.1.84 10.1016/j.bmcl.2004.08.047 10.1021/jo016090n 10.1021/jo00033a031 10.1016/S0040-4020(02)00287-9 |
| ContentType | Journal Article |
| Copyright | Copyright Taylor & Francis Group, LLC 2007 |
| Copyright_xml | – notice: Copyright Taylor & Francis Group, LLC 2007 |
| DBID | CGR CUY CVF ECM EIF NPM AAYXX CITATION 7TM 7X8 |
| DOI | 10.1080/15257770701521284 |
| DatabaseName | Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed CrossRef Nucleic Acids Abstracts MEDLINE - Academic |
| DatabaseTitle | MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) CrossRef Nucleic Acids Abstracts MEDLINE - Academic |
| DatabaseTitleList | Nucleic Acids Abstracts MEDLINE - Academic MEDLINE |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1532-2335 |
| EndPage | 1114 |
| ExternalDocumentID | 10_1080_15257770701521284 18058547 251993 |
| Genre | Original Articles Research Support, Non-U.S. Gov't Journal Article |
| GroupedDBID | --- -~X .7F .QJ 0BK 0R~ 123 29N 2DF 30N 36B 3YN 4.4 53G 5VS AAAVI AAENE AAJMT AALDU AAMIU AAPUL AAQRR ABBKH ABCCY ABDBF ABDDZ ABFIM ABJVF ABLIJ ABPEM ABPTK ABQHQ ABTAI ABXUL ACGEJ ACGFS ACPRK ACTIO ADCVX ADGTB ADXPE AEGYZ AEISY AEOZL AEPSL AEYOC AFFNX AFKVX AFOLD AFWLO AGDLA AGMYJ AHDLD AIJEM AIRXU AJWEG AKBVH AKOOK ALMA_UNASSIGNED_HOLDINGS ALQZU AQRUH AVBZW AWYRJ BLEHA CAG CCCUG CE4 COF DGEBU DKSSO EAP EBC EBD EBS EJD EMB EMK EMOBN EPL EST ESX E~A E~B F5P FUNRP FVPDL GTTXZ H13 HZ~ H~P IPNFZ J.P KYCEM M4Z NA5 NW0 O9- RIG RNANH ROSJB RTWRZ S-T SNACF SV3 TCY TFL TFT TFW TTHFI TUS TWF UT5 UU3 V1K ZGOLN ~S~ .GJ 1TA AAAJW ABJNI ABKVM ABPAQ ABXYU ABZMO ACYAP ADOGB AFWJF BDVFT BKMSO CGR CUY CVF CXCUG ECM EIF HF~ LJTGL NPM NUSFT OEUFU S10 TBQAZ TDBHL TUROJ Y6R AAYXX CITATION 7TM 7X8 |
| ID | FETCH-LOGICAL-c431t-da080a2ffdad69c1e8bff73ecfca4813fcccc0c6d600d2885525cea58c3497ec3 |
| ISSN | 1525-7770 |
| IngestDate | Sat Oct 26 00:39:01 EDT 2024 Fri Oct 25 12:04:30 EDT 2024 Fri Aug 23 02:22:10 EDT 2024 Tue Oct 15 23:35:39 EDT 2024 Tue Jun 13 19:25:19 EDT 2023 Mon May 13 12:09:25 EDT 2019 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 8-9 |
| Language | English |
| LinkModel | OpenURL |
| MergedId | FETCHMERGED-LOGICAL-c431t-da080a2ffdad69c1e8bff73ecfca4813fcccc0c6d600d2885525cea58c3497ec3 |
| Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
| PMID | 18058547 |
| PQID | 21041087 |
| PQPubID | 23462 |
| PageCount | 4 |
| ParticipantIDs | proquest_miscellaneous_21041087 informaworld_taylorfrancis_310_1080_15257770701521284 proquest_miscellaneous_69039704 pubmed_primary_18058547 crossref_primary_10_1080_15257770701521284 |
| PublicationCentury | 2000 |
| PublicationDate | 2007-01-01 |
| PublicationDateYYYYMMDD | 2007-01-01 |
| PublicationDate_xml | – month: 01 year: 2007 text: 2007-01-01 day: 01 |
| PublicationDecade | 2000 |
| PublicationPlace | United States |
| PublicationPlace_xml | – name: United States |
| PublicationTitle | Nucleosides, nucleotides & nucleic acids |
| PublicationTitleAlternate | Nucleosides Nucleotides Nucleic Acids |
| PublicationYear | 2007 |
| Publisher | Taylor & Francis Group |
| Publisher_xml | – name: Taylor & Francis Group |
| References | CIT0002 CIT0005 CIT0004 CIT0003b CIT0003a Hayashi M. (CIT0001) 1980; 8 |
| References_xml | – ident: CIT0002 doi: 10.1128/AAC.28.1.84 – ident: CIT0003b doi: 10.1016/j.bmcl.2004.08.047 – volume: 8 start-page: s65 year: 1980 ident: CIT0001 publication-title: Nucl. Acids Res. Symp. Ser. contributor: fullname: Hayashi M. – ident: CIT0003a doi: 10.1021/jo016090n – ident: CIT0004 doi: 10.1021/jo00033a031 – ident: CIT0005 doi: 10.1016/S0040-4020(02)00287-9 |
| SSID | ssj0018087 |
| Score | 1.7519938 |
| Snippet | The stereospecific synthesis of (−)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an... The stereospecific synthesis of (-)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an... |
| SourceID | proquest crossref pubmed informaworld |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 1111 |
| SubjectTerms | Adenosine - analogs & derivatives Adenosine - chemical synthesis Adenosine - chemistry carbanucleoside Methods Molecular Structure Neplanocin Nucleosides - chemical synthesis Nucleosides - chemistry Stereoisomerism stereospecific synthesis |
| Title | Stereospecific Synthesis of (−)-Neplanocin F |
| URI | https://www.tandfonline.com/doi/abs/10.1080/15257770701521284 https://www.ncbi.nlm.nih.gov/pubmed/18058547 https://search.proquest.com/docview/21041087 https://search.proquest.com/docview/69039704 |
| Volume | 26 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaWcoAL4s3yzIEDUAzO084RVVQVUvcArdRb5FdQJUhWxZFQfz0zdpJNWLYC9hCtY3uy9syOPo-dbwh5qZTmHGpooU1JM6EtFWWWU8DiJi2UZLHGeMfxqjg6zT6d5WeLxXpyaqlz6p2-_ON7Jf-jVbgHesW3ZP9Bs6NQuAHfQb9wBQ3D9a90_AUmxSLXtz9Yh-wDAOd6hhFAjhSW-bSx62-yARU0-7MjfCskMm4xWafXZOOLDoveGnwZuVz1udkch2-RVtwHTO3F1_N2_3NrYHXf2csRmBsYvAvIHCMBuA0vxv7HADfDzvyc12D0z6ESRMrObJoMFjwEJ_gkONH7U8yWy0NukMHhhlfke8MCdzvxn3HverccezgJieJQGmcIO5KQXG6i6PV3r-lYMFgFBSbP39i0h6pr5HoCrgl9YspW476TYD6l4vizh31wwd5vPRv5ZntpM1Azo7zdvXDxAObkNrnVrzyiD8GM7pCFbe6SGwdDwr975O3cnKLRnKK2jl7R1xNTig7vk9PDjycHR7RPpkE1YERHjYRByKSujTRFqWMrVF3z1Ooaee3jtNbwYbowgIBNIkQOw9VW5kKnWcmtTh-QvaZt7CMSWWlLm0D3AsC0YlwVHGBhzlNorVQml-TNMBvVOnCmVHFPRbs1i0vCpvNVOR-oqkNWme3mlfvpliS_okt6xaNeDLqoYGpxZ0w2tu1-VEnMMujDd7coSgbInYGMh0GJm5H1NvB4Z80TcnPz33hK9txFZ58BlHXqube-X7PPlHo |
| link.rule.ids | 315,783,787,27936,27937,60214,61003 |
| linkProvider | Taylor & Francis |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3JTsMwEB1BOcCFfSlbc-AASC5uk9jJEVVUZeulReIW2Y4tIVBa0VQCvoAzn8iXMM4ClO1Arhk7Y4-X5_HkDcCelIpzfEOYikPiBUqTIPR8glg8dpkUtKGsv-OyyzpX3tm1f1043EZFWKU9Q5ucKCJbq-3kts7oMiTuyObs4ZzjaLW7Dy6w0zDDLPmX_YWDdt9vEQKaJciz4sTKl7eaP1UxsS9NsJb-jj2zPai9AFGpfR56clsfp7Kunr4QO_6_eYswX8BT5zgfT0swpZNlmG2VWeFWoN5DQ2jLL54F8zm9xwQh5Ohm5AyMs__6_HJAunp4JxI0euK0V-GqfdJvdUiRc4EohBIpiQVqIJrGxCJmoWroQBrDXa2MpT9vuEbhQxWLESjFzSDwUVelhR8o1wu5Vu4aVJJBojfA0UKHuonFGWIuSblkHNGDz12UltITVTgsezwa5tQaUaNgLP3WBVWgn20SpZk_w-TJR76LR-lDWgX_jyLuH5-qlfaOsHPtBYpI9GA8ivB47GEZ_rsECykCPIp1rOcD5aNlAcWTmcc3_6lVDWY7_cuL6OK0e74Fc7mL2XqCtqGS3o_1DmKjVO5mE-ANJm0DKA |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3JTsMwELWgSMCFfSlbc-AASC5Oszg5okJVtgqpVOotsh1bQqC0IqkEfAFnPpEvYZwFKKU9NNfMOLZnYj-PR28QOuRcUApvsCtCH9uekNjzbQcDFg8tlzNiCh3vuG25zY591XW6eW5OnKdV6jO0yogi0rVa_9z9UBUZcae6ZA-lFJxVbz6wvs6iOUABRLu5RVrflwgeSevjaXGs5YtLzf-aGNqWhkhLx0PPdAtqLGd1VuOUuVBnnjxWBwmvirc_vI5Tj24FLeXg1DjLvGkVzchoDS3Ui5pw66jaBjNIzS6epvIZ7dcIAGT8EBs9ZRx9vn8c45bsP7EITB4ZjQ3UaVzc15s4r7iABQCJBIcMesBqSoUsdH1hSo8rRS0plCY_Ny0l4CHCDQEmhTXPc6CvQjLHE5btUymsTVSKepHcRoZk0pc1UHcBcXFCuUsBOzjUAmnObVZGJ8WEB_2MWCMwc77SkSkoI_LbJEGSRjNUVnpkVDxIXpIyciaoWBM-VSnMHcDk6usTFsneIA7gcGyDDh0v4foE4B2BNrYyP_kZmUfgXGbTnSl7VUHzd-eN4Oaydb2LFrP4sg4D7aFS8jyQ-wCMEn6Quv8XDE4B1Q |
| 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=Stereospecific+synthesis+of+%28-%29-neplanocin+F&rft.jtitle=Nucleosides%2C+nucleotides+%26+nucleic+acids&rft.au=Ropero%2C+Sergio+Rodriguez&rft.au=Edmont%2C+Dolor%C3%A8s&rft.au=Math%C3%A9%2C+Christophe&rft.au=P%C3%A9rigaud%2C+Christian&rft.date=2007-01-01&rft.issn=1525-7770&rft.volume=26&rft.issue=8-9&rft.spage=1111&rft_id=info:doi/10.1080%2F15257770701521284&rft_id=info%3Apmid%2F18058547&rft.externalDocID=18058547 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1525-7770&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1525-7770&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1525-7770&client=summon |