Synthesis of dihalocarbene derivatives of arglabin
Dibromocarbene and bisdichlorocarbene derivatives of the available sesquiterpene lactone arglabin were synthesized for the first time. The structures of the molecules were established by spectra methods and XSA.
Saved in:
| Published in | Chemistry of natural compounds Vol. 41; no. 5; pp. 552 - 555 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
NEW YORK
Springer Nature
01.09.2005
|
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | Dibromocarbene and bisdichlorocarbene derivatives of the available sesquiterpene lactone arglabin were synthesized for the first time. The structures of the molecules were established by spectra methods and XSA. |
|---|---|
| AbstractList | Dibromocarbene and bisdichlorocarbene derivatives of the available sesquiterpene lactone arglabin were synthesized for the first time. The structures of the molecules were established by spectra methods and XSA. |
| Author | Adekenov, SM Dzhalmakhanbetova, RI Bagryanskaya, IY Gatilov, YV Kulyyasov, AT Raldugin, VA Shakirov, MM |
| Author_xml | – sequence: 1 givenname: RI surname: Dzhalmakhanbetova fullname: Dzhalmakhanbetova, RI email: arglabin@mail.krg.kz – sequence: 2 givenname: VA surname: Raldugin fullname: Raldugin, VA email: raldugin@nioch.nsc.ru – sequence: 3 givenname: IY orcidid: 0000-0001-7760-5540 surname: Bagryanskaya fullname: Bagryanskaya, IY – sequence: 4 givenname: YV surname: Gatilov fullname: Gatilov, YV – sequence: 5 givenname: MM surname: Shakirov fullname: Shakirov, MM – sequence: 6 givenname: AT surname: Kulyyasov fullname: Kulyyasov, AT – sequence: 7 givenname: SM surname: Adekenov fullname: Adekenov, SM |
| BookMark | eNqNkE9PwzAMxSM0JLbBB-C2Owo4cZumR1TxT5rEAThXSeqwoJGipozt25MxxBn5YFt-70k_z9gk9pEYOxdwKQCqqyRAAXCAkoOEgm-P2FSUFXKNWk_YFABqjgLhhM1SesurVkpPmXzaxXFFKaRF7xddWJl178xgKdKioyFszBg29HM0w-va2BBP2bE360Rnv33OXm5vnpt7vny8e2iul9zJohw5eVfWHVRYSyQtjPO5auyExU7ZymtbCDCKsETqTGXJaSmsEaXsPDpjcc7EIdcNfUoD-fZjCO9m2LUC2j10e4BuM3S7h2632XNx8HyR7X1ygaKjP1-mlljUSmOehMpq_X91E8b8iz42_Wcc8Rum525F |
| CitedBy_id | crossref_primary_10_1016_j_fitote_2015_11_018 crossref_primary_10_1016_j_cbi_2015_08_015 crossref_primary_10_3987_COM_07_10998 crossref_primary_10_1002_cmdc_202400045 crossref_primary_10_2174_1385272824666200312125734 crossref_primary_10_1016_j_tetasy_2014_10_017 crossref_primary_10_1007_s11172_015_0930_6 |
| Cites_doi | 10.1016/0040-4020(79)80099-X |
| ContentType | Journal Article |
| DBID | 1KM BLEPL DTL FZXEZ AAYXX CITATION |
| DOI | 10.1007/s10600-005-0204-x |
| DatabaseName | Index Chemicus Web of Science Core Collection Science Citation Index Expanded Web of Science - Science Citation Index Expanded - 2005 CrossRef |
| DatabaseTitle | Web of Science CrossRef |
| DatabaseTitleList | Web of Science |
| Database_xml | – sequence: 1 dbid: 1KM name: Index Chemicus url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.IC sourceTypes: Enrichment Source Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1573-8388 |
| EndPage | 555 |
| ExternalDocumentID | 10_1007_s10600_005_0204_x 000234968300016 |
| GroupedDBID | -53 -5E -5G -BR -EM -XW -Y2 -~C -~X .86 .VR 06C 06D 0R~ 0VY 1KM 1N0 29B 29~ 2J2 2JN 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 4.4 406 408 409 40D 40E 53G 5GY 5VS 67Z 6NX 78A 8TC 8UJ 95- 95. 95~ 96X AAAVM AABHQ AACDK AAHBH AAHNG AAIAL AAJBT AAJKR AANXM AANZL AARHV AARTL AASML AATNV AATVU AAUYE AAWCG AAYIU AAYQN AAYTO ABAKF ABBBX ABBXA ABDBF ABDZT ABECU ABFTV ABHLI ABHQN ABJNI ABJOX ABKCH ABKTR ABMNI ABMQK ABNWP ABQBU ABSXP ABTEG ABTKH ABTMW ABULA ABWNU ABXPI ACAOD ACBXY ACDTI ACGFS ACHSB ACHXU ACIPQ ACIWK ACKNC ACMDZ ACMLO ACOKC ACOMO ACSNA ACZOJ ADHHG ADHIR ADIMF ADINQ ADKNI ADKPE ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEFQL AEGAL AEGNC AEJHL AEJRE AEKMD AEMSY AENEX AEOHA AEPYU AESKC AETLH AEVLU AEXYK AFBBN AFGCZ AFLOW AFQWF AFWTZ AFZKB AGAYW AGDGC AGJBK AGMZJ AGQEE AGQMX AGRTI AGWIL AGWZB AGYKE AHBYD AHKAY AHSBF AHYZX AIAKS AIGIU AIIXL AILAN AITGF AJBLW AJRNO ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AMYQR AOCGG ARMRJ ASPBG AVWKF AXYYD AZFZN B-. B0M BA0 BDATZ BGNMA BLEPL CAG COF CS3 CSCUP DDRTE DL5 DNIVK DPUIP DTL DU5 EAD EAP EBLON EBS EIOEI EJD EMK EPL ESBYG ESX FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC G-Y G-Z GGCAI GGRSB GJIRD GNWQR GQ6 GQ7 GQ8 GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED GXS HF~ HG6 HMJXF HQYDN HRMNR HVGLF HZ~ IAO IFM IHE IJ- IKXTQ ISR ITM IWAJR IXC IZIGR IZQ I~X I~Z J-C JBSCW JCJTX JZLTJ KDC KOV LAK LLZTM M4Y MA- N2Q NB0 NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OAM OVD P19 P2P P9N PF0 PT4 PT5 QOK QOR QOS R89 R9I RHV RNI RNS ROL RPX RSV RZC RZE S16 S27 S3B SAP SDH SDM SHX SISQX SJYHP SMD SNE SNPRN SNX SOHCF SOJ SPISZ SRMVM SSLCW STPWE SZ9 SZN T13 TEORI TSG TSK TSV TUC TUS TWZ U2A U9L UG4 UOJIU UTJUX UZXMN VC2 VFIZW W23 W48 WIP WJK WK8 XU3 YLTOR Z7U Z7V Z7W Z87 Z8O Z8P Z8Q Z91 Z92 ZOVNA ~8M ~A9 ~EX 1SB 2.D 28- 5QI 642 AAEOY AAYXX ACUDM AEFIE AFEXP AFFNX AGGDS AGJZZ AHAVH BBWZM CITATION GRRUI H13 KOW NDZJH R4E RZK S1Z S26 S28 SCG SCLPG SDE T16 W4F |
| ID | FETCH-LOGICAL-c245t-efc59d073923e81acfcfc93d1b3d6b7f8b410a6e353eda7bec821ba152df3cab3 |
| ISICitedReferencesCount | 3 |
| ISICitedReferencesURI | https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000234968300016 |
| ISSN | 0009-3130 |
| IngestDate | Thu Sep 12 17:28:16 EDT 2024 Wed Sep 18 05:21:02 EDT 2024 Fri Oct 11 20:14:30 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 5 |
| Keywords | NMR sesquiterpene lactones x-ray structure analysis arglabin dihalocarbenes interphase catalysis |
| Language | English |
| LinkModel | OpenURL |
| LogoURL | https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg |
| MergedId | FETCHMERGED-LOGICAL-c245t-efc59d073923e81acfcfc93d1b3d6b7f8b410a6e353eda7bec821ba152df3cab3 |
| ORCID | 0000-0001-7760-5540 |
| PageCount | 4 |
| ParticipantIDs | webofscience_primary_000234968300016 webofscience_primary_000234968300016CitationCount crossref_primary_10_1007_s10600_005_0204_x |
| PublicationCentury | 2000 |
| PublicationDate | 2005-09-01 |
| PublicationDateYYYYMMDD | 2005-09-01 |
| PublicationDate_xml | – month: 09 year: 2005 text: 2005-09-01 day: 01 |
| PublicationDecade | 2000 |
| PublicationPlace | NEW YORK |
| PublicationPlace_xml | – name: NEW YORK |
| PublicationTitle | Chemistry of natural compounds |
| PublicationTitleAbbrev | CHEM NAT COMPD |
| PublicationYear | 2005 |
| Publisher | Springer Nature |
| Publisher_xml | – name: Springer Nature |
| References | SALAZAR, I (WOS:A1979GX57500001) 1979; 35 FAZYLOVA AS (WOS:000234968300016.4) 1998 KOSTIKOV, RR (WOS:A1975AM52100047) 1975; 11 FAZYLOVA AS (WOS:000234968300016.3) 1998 JALMAKHANBETOVA RI (WOS:000234968300016.5) 2004 ADEKENOV, SM (WOS:A1991FK46700006) 1991 ADEKENOV, SM (WOS:A1982PT77000033) 1982 JALMAKHANBETOVA RI (WOS:000234968300016.6) 2003 I. Salazar (204_CR1) 1979; 35 204_CR3 204_CR5 204_CR4 204_CR7 204_CR6 204_CR8 R. R. Kostikov (204_CR2) 1975; 11 |
| References_xml | – start-page: 655 year: 1982 ident: WOS:A1982PT77000033 article-title: ARGLABIN, A NEW SESQUITERPENE LACTONE FROM ARTEMISIA-GLABELLA publication-title: KHIMIYA PRIRODNYKH SOEDINENII contributor: fullname: ADEKENOV, SM – volume: 35 start-page: 815 year: 1979 ident: WOS:A1979GX57500001 article-title: CARBOFLUORINATION OF PSEUDOGUAIANOLIDE SESQUITERPENIC LACTONES publication-title: TETRAHEDRON contributor: fullname: SALAZAR, I – start-page: 64 year: 2004 ident: WOS:000234968300016.5 publication-title: 2 INT C NAT PROD PHY contributor: fullname: JALMAKHANBETOVA RI – volume: 11 start-page: 1767 year: 1975 ident: WOS:A1975AM52100047 article-title: 2-PHASE METHOD FOR PREPARATION OF GEM-DIHALOCYCLOPROPANES IN PRESENCE OF CROWN-ETHERS publication-title: ZHURNAL ORGANICHESKOI KHIMII contributor: fullname: KOSTIKOV, RR – start-page: 8 year: 1998 ident: WOS:000234968300016.3 publication-title: KHIM PRIR SOEDIN contributor: fullname: FAZYLOVA AS – start-page: 33 year: 1991 ident: WOS:A1991FK46700006 article-title: REACTIONS BY BINARY BOND AND ARGLABIN EPOXY GROUP publication-title: KHIMIYA PRIRODNYKH SOEDINENII contributor: fullname: ADEKENOV, SM – start-page: 339 year: 1998 ident: WOS:000234968300016.4 publication-title: KHIM PRIR SOEDIN contributor: fullname: FAZYLOVA AS – start-page: 23 year: 2003 ident: WOS:000234968300016.6 publication-title: P 5 INT S CHEM NAT C contributor: fullname: JALMAKHANBETOVA RI – volume: 35 start-page: 815 year: 1979 ident: 204_CR1 publication-title: Tetrahedron doi: 10.1016/0040-4020(79)80099-X contributor: fullname: I. Salazar – ident: 204_CR8 – ident: 204_CR3 – ident: 204_CR4 – ident: 204_CR6 – ident: 204_CR7 – ident: 204_CR5 – volume: 11 start-page: 1767 year: 1975 ident: 204_CR2 publication-title: Zh. Org. Khim. contributor: fullname: R. R. Kostikov |
| SSID | ssj0008668 |
| Score | 1.7283248 |
| Snippet | Dibromocarbene and bisdichlorocarbene derivatives of the available sesquiterpene lactone arglabin were synthesized for the first time. The structures of the... |
| Source | Web of Science |
| SourceID | crossref webofscience |
| SourceType | Aggregation Database Enrichment Source Index Database |
| StartPage | 552 |
| SubjectTerms | Chemistry Chemistry, Medicinal Chemistry, Organic Life Sciences & Biomedicine Pharmacology & Pharmacy Physical Sciences Science & Technology |
| Title | Synthesis of dihalocarbene derivatives of arglabin |
| URI | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000234968300016 |
| Volume | 41 |
| WOS | 000234968300016 |
| WOSCitedRecordID | wos000234968300016 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9NAEF5F5QAXxFOEl3zoichW7H3YewwF1HLgQoPKKdqXW9TiIMupSMWPZ_bhtQNFapEly7K9o7VnPDPrmfkGoX0sRKkNMylWnKdECJJWqmbAEGVUlRPFapfl-4kdLsnHE3oymfwaV5d0MlNX19aV_A9X4Rzw1VbJ3oKzkSicgGPgL-yBw7C_EY8_bxvw3wKkyLtvZ8JaplaC-gI90rq-ZQFUdtGCmywDynYPTND3enPJHMIDcNgUc9tpaeg3fwVkv4vzM9FI060vvbOZzY6yIUR0oTenHovgSzZbxAtvxWm7BVN4LrZu1FE2-7qJCT8wuYv1pTMBmwwG7vx_oDHBatCpHDR5iK6YoEZLnFbYN-zr9SzJR_JER0qTegzbYH-ph-39S7XP-1Jn5mrhbV35nKQ_BzvWx-7_MG8x6XAAaLYkVkBiZUnYFcidouTUJoQui0W04xVjVd-Hzz5fHxP3hZe7s9jxaq7xYJy3cvwA3Q_LjGThZeYhmpjmEbobOf4YFVF2knWd7MhOMpIde7GXnSdo-eH98cFhGvpnpKogtEtNrSjXNhRbYFPlQtWwcaxziTWTZV1Jks8FM5hio0UJX3NV5FKAR6drrITET9Fes27MM5RIJqXJgRivDVGFENpgA16PwbzWRuRT9KZ__tUPD5Oy-uf7nqL98RuKAxz4EuGswm4lMkX5TW47CFj2FsOhe36bebxA9zwQr_2h9hLtde3GvAIXs5OvnST8BiN6eG4 |
| link.rule.ids | 315,786,790,27955,27956 |
| linkProvider | Springer Nature |
| 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=Synthesis+of+Dihalocarbene+Derivatives+of+Arglabin&rft.jtitle=Chemistry+of+natural+compounds&rft.au=Dzhalmakhanbetova%2C+R.+I.&rft.au=Raldugin%2C+V.+A.&rft.au=Bagryanskaya%2C+I.+Yu&rft.au=Gatilov%2C+Yu.+V.&rft.date=2005-09-01&rft.issn=0009-3130&rft.eissn=1573-8388&rft.volume=41&rft.issue=5&rft.spage=552&rft.epage=555&rft_id=info:doi/10.1007%2Fs10600-005-0204-x&rft.externalDBID=n%2Fa&rft.externalDocID=10_1007_s10600_005_0204_x |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0009-3130&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0009-3130&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0009-3130&client=summon |