Efficient Synthesis of Pyrrolo[1,2-f]phenanthridine Derivatives via Dipolar Cycloaddition of Phenanthridine, Activated Acetylenes, and Ethyl Bromopyruvate

The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [...

Full description

Saved in:
Bibliographic Details
Published inSynthetic communications Vol. 44; no. 1; pp. 76 - 81
Main Authors Mehrabi, Hossein, Pishahang, Jaleh
Format Journal Article
LanguageEnglish
Published PHILADELPHIA Taylor & Francis Group 02.01.2014
Taylor & Francis
Taylor & Francis Ltd
Subjects
Online AccessGet full text
ISSN0039-7911
1532-2432
DOI10.1080/00397911.2013.789525

Cover

Abstract The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.]
AbstractList The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resource(s): Full experimental and spectral details.]
The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.]
The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed. The reactions afforded the corresponding pyrrolo[1,2-f]phenanthridine derivatives in good yields without using any catalyst and activation. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] [PUBLICATION ABSTRACT]
Author Mehrabi, Hossein
Pishahang, Jaleh
Author_xml – sequence: 1
  givenname: Hossein
  surname: Mehrabi
  fullname: Mehrabi, Hossein
  email: mehraby_h@yahoo.com
  organization: Department of Chemistry , Rafsanjan Vali-e-Asr University
– sequence: 2
  givenname: Jaleh
  surname: Pishahang
  fullname: Pishahang, Jaleh
  organization: Department of Chemistry , Rafsanjan Vali-e-Asr University
BookMark eNqNkcuKFDEUhoOMYM_oG7gIuLSrTSp1dSNjTXuBAQV1JRJO50JnSCdlku6hXsWnNWXNLHShrnLI-b5z4Pzn6Mx5pxB6SsmGko68IIT1bU_ppiSUbdqur8v6AVrRmpVFWbHyDK1mpJiZR-g8xhtCaJ25Ffqx1doIo1zCnyaX9iqaiL3GH6cQvPVf6bos9LdxrxzkbjDSOIWvVDAnSOakIj4ZwFdm9BYCHiZhPUhpkvHu15TfvDW-FGkWlcyVSpNVTsU1BifxNu0ni18Hf_DjFI4z9Bg91GCjenL3XqAvb7afh3fF9Ye374fL60IwVqdi1zVCtVKwHpjs664BqWjf5E_CdlAr2laSdtC2jEHPQPYN6yXVBETb6Laj7AI9W-aOwX8_qpj4jT8Gl1dyWlW0abqOsUw9X6hbtfM6zicTio_BHCBMnOT7lnWd-VyRNtPd_9ODSTBfbPBHl7L6clFF8DEGpbm466cAxnJK-Bw6vw-dz6HzJfQsV3_I9zv_ob1aNOO0Dwe49cFKnmCyPugATpjI2V8n_ASOKMWy
CitedBy_id crossref_primary_10_1039_C4CC06643J
crossref_primary_10_1016_j_mencom_2020_01_004
crossref_primary_10_1016_j_cclet_2014_05_024
crossref_primary_10_1007_s13738_018_1393_0
crossref_primary_10_1002_chin_201424169
Cites_doi 10.1055/s-2007-969864
10.1002/cjoc.201100238
10.1002/jhet.205
10.1039/b905383b
10.1021/np50035a007
10.1016/S0223-5234(01)01289-2
10.1016/j.bmcl.2004.10.054
10.1021/jm00200a011
10.1016/j.tetlet.2006.06.113
10.1016/j.tet.2011.03.085
10.1055/s-0031-1290447
10.1080/00397911.2011.605240
10.1021/jo00057a029
10.1021/ja01463a047
10.1135/cccc19942641
10.1016/j.tet.2003.11.093
10.1021/ja803338m
10.1039/jr9620003758
ContentType Journal Article
Copyright Copyright Taylor & Francis Group, LLC 2014
Copyright Taylor and Francis Group, LLC
Copyright_xml – notice: Copyright Taylor & Francis Group, LLC 2014
– notice: Copyright Taylor and Francis Group, LLC
DBID AAYXX
CITATION
17B
1KM
BLEPL
DTL
EGQ
GNMZZ
DOI 10.1080/00397911.2013.789525
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Web of Science - Science Citation Index Expanded - 2014
DatabaseTitle CrossRef
Web of Science
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 1532-2432
EndPage 81
ExternalDocumentID 3097680121
000325514400007
10_1080_00397911_2013_789525
789525
Genre Feature
GroupedDBID ---
-~X
.7F
.QJ
0BK
0R~
123
29Q
30N
4.4
5VS
AAENE
AAJMT
AALDU
AAMIU
AAPUL
AAQRR
ABCCY
ABDBF
ABFIM
ABHAV
ABJNI
ABLIJ
ABPAQ
ABPEM
ABTAI
ABXUL
ABXYU
ACGEJ
ACGFS
ACIWK
ACNCT
ACTIO
ACUHS
ADCVX
ADGTB
ADXPE
AEISY
AENEX
AEOZL
AEPSL
AEYOC
AFKVX
AGDLA
AGMYJ
AHDZW
AIJEM
AJWEG
AKBVH
AKOOK
ALMA_UNASSIGNED_HOLDINGS
ALQZU
AQRUH
AVBZW
AWYRJ
BLEHA
CCCUG
CE4
CS3
DGEBU
DKSSO
DU5
E.-
EAP
EBD
EBS
EJD
EMK
EPL
EST
ESX
E~A
E~B
F5P
GTTXZ
H13
HF~
HZ~
H~P
IPNFZ
J.P
KYCEM
M4Z
NA5
NW0
O9-
P2P
RIG
RNANH
ROSJB
RTWRZ
S-T
SNACF
TBQAZ
TCY
TFL
TFT
TFW
TN5
TTHFI
TUROJ
TUS
TWF
UT5
UU3
YNT
ZGOLN
~S~
AAGDL
AAHIA
AAYXX
AFRVT
AIYEW
CITATION
TASJS
17B
1KM
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
ID FETCH-LOGICAL-c335t-b86ce7dc39a3d9586ade1966ce03ba5e174d18a7733a93ad9639d1f0ac76f7813
ISICitedReferencesCount 5
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000325514400007
ISSN 0039-7911
IngestDate Wed Aug 13 05:57:26 EDT 2025
Wed Aug 06 05:25:34 EDT 2025
Fri Sep 26 20:46:15 EDT 2025
Wed Oct 01 01:31:55 EDT 2025
Thu Apr 24 23:10:05 EDT 2025
Wed Dec 25 09:00:23 EST 2024
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords three-component reactions
2-f]phenanthridines
ANALOGS
AZOMETHINE YLIDES
pyrrolo
AGENTS
Ethyl bromopyruvate
phenanthridine
DIMETHYL ACETYLENEDICARBOXYLATE
Language English
LinkModel OpenURL
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c335t-b86ce7dc39a3d9586ade1966ce03ba5e174d18a7733a93ad9639d1f0ac76f7813
Notes SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 14
PQID 1441668833
PQPubID 216155
PageCount 6
ParticipantIDs crossref_citationtrail_10_1080_00397911_2013_789525
crossref_primary_10_1080_00397911_2013_789525
informaworld_taylorfrancis_310_1080_00397911_2013_789525
webofscience_primary_000325514400007CitationCount
webofscience_primary_000325514400007
proquest_journals_1441668833
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2014-01-02
PublicationDateYYYYMMDD 2014-01-02
PublicationDate_xml – month: 01
  year: 2014
  text: 2014-01-02
  day: 02
PublicationDecade 2010
PublicationPlace PHILADELPHIA
PublicationPlace_xml – name: PHILADELPHIA
– name: Philadelphia
PublicationTitle Synthetic communications
PublicationTitleAbbrev SYNTHETIC COMMUN
PublicationYear 2014
Publisher Taylor & Francis Group
Taylor & Francis
Taylor & Francis Ltd
Publisher_xml – name: Taylor & Francis Group
– name: Taylor & Francis
– name: Taylor & Francis Ltd
References CIT0010
CIT0001
CIT0012
CIT0011
CIT0003
CIT0014
CIT0002
Buyanov V. N. (CIT0005) 1994; 28
CIT0013
CIT0016
CIT0004
CIT0015
CIT0007
CIT0018
CIT0006
CIT0017
CIT0009
CIT0008
CIT0019
Richmond, CJ (WOS:000259553700051) 2008; 130
Yavari, I (WOS:000308225000016) 2012
ACHESON, RM (WOS:A19624218B00002) 1962
Wu, L (WOS:000301541600020) 2012; 30
Buyanov, V. N. (BCI:BCI199497515511) 1994; 28
Ming, L. (000325514400007.10) 2011; 67
CHATTOPADHYAY, S (WOS:A1983RW95900016) 1983; 49
Almerico, AM (WOS:000174532700001) 2002; 37
Kitson, PJ (WOS:000267571100020) 2009
Mehrabi, H (WOS:000310953600013) 2013; 43
BOEKELHEIDE, V (WOS:A19613059B00004) 1961; 83
ZEECHENG, RKY (WOS:A1978EJ53000011) 1978; 21
Yavari, I (WOS:000239885000006) 2006; 47
Harayama, T (WOS:000188785600020) 2004; 60
PADWA, A (WOS:A1993KN98900029) 1993; 58
Yue, GH (WOS:000226344800040) 2005; 15
PETTIT, GR (WOS:A1984TR54300007) 1984; 47
POTACEK, M (WOS:A1994QD86300009) 1994; 59
Kianmehr, E (WOS:000272878500018) 2009; 46
References_xml – ident: CIT0002
  doi: 10.1055/s-2007-969864
– ident: CIT0014
  doi: 10.1002/cjoc.201100238
– ident: CIT0013
  doi: 10.1002/jhet.205
– ident: CIT0008
  doi: 10.1039/b905383b
– ident: CIT0003
  doi: 10.1021/np50035a007
– ident: CIT0006
  doi: 10.1016/S0223-5234(01)01289-2
– ident: CIT0012
  doi: 10.1016/j.bmcl.2004.10.054
– ident: CIT0004
  doi: 10.1021/jm00200a011
– ident: CIT0017
  doi: 10.1016/j.tetlet.2006.06.113
– ident: CIT0018
  doi: 10.1016/j.tet.2011.03.085
– volume: 28
  start-page: 10
  year: 1994
  ident: CIT0005
  publication-title: Khim.-farm. Zh.
– ident: CIT0011
  doi: 10.1055/s-0031-1290447
– ident: CIT0019
  doi: 10.1080/00397911.2011.605240
– ident: CIT0010
  doi: 10.1021/jo00057a029
– ident: CIT0009
  doi: 10.1021/ja01463a047
– ident: CIT0016
  doi: 10.1135/cccc19942641
– ident: CIT0001
  doi: 10.1016/j.tet.2003.11.093
– ident: CIT0007
  doi: 10.1021/ja803338m
– ident: CIT0015
  doi: 10.1039/jr9620003758
– volume: 59
  start-page: 2641
  year: 1994
  ident: WOS:A1994QD86300009
  article-title: PHENANTHRIDINIUM-BASED AZOMETHINE YLIDES IN 1,3-DIPOLAR CYCLOADDITION WITH DIMETHYL ACETYLENEDICARBOXYLATE
  publication-title: COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS
– volume: 58
  start-page: 1144
  year: 1993
  ident: WOS:A1993KN98900029
  article-title: CYCLOADDITION REACTIONS OF PYRIDINIUM AND RELATED AZOMETHINE YLIDES
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– start-page: 4067
  year: 2009
  ident: WOS:000267571100020
  article-title: A new C-C bond forming annulation reaction leading to pH switchable heterocycles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b905383b
– volume: 83
  start-page: 458
  year: 1961
  ident: WOS:A19613059B00004
  article-title: FORMATION OF PYRROCOLINES BY REACTION OF DIMETHYL ACETYLENEDICARBOXYLATE WITH HETEROCYCLIC ZWITTERIONS
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 21
  start-page: 199
  year: 1978
  ident: WOS:A1978EJ53000011
  article-title: ANTI-LEUKEMIC ACTIVITY OF UNGEREMINE AND RELATED COMPOUNDS - PREPARATION OF ANALOGS OF UNGEREMINE BY A PRACTICAL PHOTO-CHEMICAL REACTION
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
– start-page: 2103
  year: 2012
  ident: WOS:000308225000016
  article-title: Novel Synthesis of Functionalized Indolizine Derivatives from Huisgen's Zwitterions and 1-Methylimidazole/Dichloroketene Adduct
  publication-title: SYNLETT
  doi: 10.1055/s-0031-1290447
– volume: 43
  start-page: 611
  year: 2013
  ident: WOS:000310953600013
  article-title: SYNTHESIS OF FUNCTIONALIZED PYRIDO[1,2-f]PHENANTHRIDINES FROM PHENANTHRIDINE, ACTIVATED ACETYLENES, AND ARYLIDENEMALONONITRILES
  publication-title: SYNTHETIC COMMUNICATIONS
  doi: 10.1080/00397911.2011.605240
– volume: 46
  start-page: 1203
  year: 2009
  ident: WOS:000272878500018
  article-title: Efficient Synthesis of Pyrrolo[2,1-a]isoquinoline and Pyrrolo[1,2-a]quinoline Derivatives in Aqueous Media
  publication-title: JOURNAL OF HETEROCYCLIC CHEMISTRY
  doi: 10.1002/jhet.205
– volume: 67
  start-page: 3638
  year: 2011
  ident: 000325514400007.10
  article-title: Novel regio-and stereo-selectivity: Synthesis of dihydropyrrolo[1,2-f]phenanthridines via isocyanide-based multicomponent reaction
  publication-title: Tetrahedron
– volume: 37
  start-page: 3
  year: 2002
  ident: WOS:000174532700001
  article-title: Pyrrolo[1,2-f]phenanthridines and related non-rigid analogues as antiviral agents
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
– volume: 28
  start-page: 10
  year: 1994
  ident: BCI:BCI199497515511
  article-title: Pyrrolophenanthridines: Synthesis and antitumor properties
  publication-title: Khimiko-Farmatsevticheskii Zhurnal
– volume: 60
  start-page: 1611
  year: 2004
  ident: WOS:000188785600020
  article-title: Concise synthesis of pyrrolophenanthridine alkaloids using a Pd-mediated biaryl coupling reaction with regioselective C-H activation via the intramolecular coordination of the amine to Pd
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2003.11.093
– start-page: 3758
  year: 1962
  ident: WOS:A19624218B00002
  article-title: ADDITION REACTIONS OF HETEROCYCLIC COMPOUNDS .11. CONSTITUTION OF SOME ADDUCTS FROM PHENANTHRIDINE AND DIMETHYL ACETYLENEDICARBOXYLATE
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY
– volume: 47
  start-page: 796
  year: 1984
  ident: WOS:A1984TR54300007
  article-title: ANTINEOPLASTIC AGENTS .99. AMARYLLIS-BELLADONNA
  publication-title: JOURNAL OF NATURAL PRODUCTS
– volume: 130
  start-page: 13059
  year: 2008
  ident: WOS:000259553700051
  article-title: Realization of a "Lockable" molecular switch via pH- and redox-modulated cyclization
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja803338m
– volume: 15
  start-page: 453
  year: 2005
  ident: WOS:000226344800040
  article-title: Synthesis of a library of benzoindolizines using poly(ethylene glycol) as soluble support
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2004.10.054
– volume: 47
  start-page: 6037
  year: 2006
  ident: WOS:000239885000006
  article-title: A synthesis of pyrrolo[2,1-a]isoquinolines through the reaction of activated acetylenes and isoquinoline in the presence of ethyl bromopyruvate
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2006.06.113
– volume: 49
  start-page: 252
  year: 1983
  ident: WOS:A1983RW95900016
  article-title: CHEMICAL-CONSTITUENTS OF AMARYLLIDACEAE .4. EFFECTS OF HIPPADINE, AN AMARYLLIDACEAE ALKALOID, ON TESTICULAR FUNCTION IN RATS
  publication-title: PLANTA MEDICA
– volume: 30
  start-page: 590
  year: 2012
  ident: WOS:000301541600020
  article-title: Efficient Synthesis of Pyrrolo[2,1-a]isoquinoline and Pyrrolo[1,2-a]quinoline Derivatives via One-pot Two-step Metal-catalyzed Three-component Reactions
  publication-title: CHINESE JOURNAL OF CHEMISTRY
  doi: 10.1002/cjoc.201100238
SSID ssj0015789
Score 2.0436392
Snippet The three-component reactions of phenanthridine, activated acetylenes, and ethyl bromopyruvate through both of simultaneous and stepwise process are surveyed....
Source Web of Science
SourceID proquest
webofscience
crossref
informaworld
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 76
SubjectTerms Chemistry
Chemistry, Organic
Ethyl bromopyruvate
phenanthridine
Physical Sciences
pyrrolo[1,2-f]phenanthridines
Science & Technology
three-component reactions
Title Efficient Synthesis of Pyrrolo[1,2-f]phenanthridine Derivatives via Dipolar Cycloaddition of Phenanthridine, Activated Acetylenes, and Ethyl Bromopyruvate
URI https://www.tandfonline.com/doi/abs/10.1080/00397911.2013.789525
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000325514400007
https://www.proquest.com/docview/1441668833
Volume 44
WOS 000325514400007
WOSCitedRecordID wos000325514400007
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVEBS
  databaseName: EBSCO Academic Search Ultimate
  customDbUrl: https://search.ebscohost.com/login.aspx?authtype=ip,shib&custid=s3936755&profile=ehost&defaultdb=asn
  eissn: 1532-2432
  dateEnd: 20241003
  omitProxy: true
  ssIdentifier: ssj0015789
  issn: 0039-7911
  databaseCode: ABDBF
  dateStart: 20010101
  isFulltext: true
  titleUrlDefault: https://search.ebscohost.com/direct.asp?db=asn
  providerName: EBSCOhost
– providerCode: PRVLSH
  databaseName: aylor and Francis Online
  customDbUrl:
  mediaType: online
  eissn: 1532-2432
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0015789
  issn: 0039-7911
  databaseCode: AHDZW
  dateStart: 19970101
  isFulltext: true
  providerName: Library Specific Holdings
– providerCode: PRVAWR
  databaseName: Taylor & Francis Science and Technology Library-DRAA
  customDbUrl:
  eissn: 1532-2432
  dateEnd: 99991231
  omitProxy: false
  ssIdentifier: ssj0015789
  issn: 0039-7911
  databaseCode: 30N
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: http://www.tandfonline.com/page/title-lists
  providerName: Taylor & Francis
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3dbtowFLYYvdhupv1qbN3ki_aqTUXixHEuGQWhqu2QBhraNEWO46hIFBgNldij7J32TjsnTkKioq7bTYSCnRjO5_Nn-zuEHERCJJH2A0twLSxXeZ4VOW1p8dhV4EAHcdvG08gXl3wwds8m3qTR-F3ZtbROoxP1c-e5kv-RKtwDueIp2X-QbPlQuAGfQb5wBQnD9UEy7mX8D7ia_3kzB08uJxcZblYr0GmH3kdQU13HwiriuJVLYlGEaYx-5SkM7zbj_L45up1K0HxLjHGPuhs1W-Aeo8KRHNb6ZZpEZRXRwFHtKJ1uZjon-8cMfA_EPgO8LK4Xy81qjc2q3q8ZJVLEquq5lNKtv9BXKxmZOtpgvPW0RO4Qi0QXue0zMGpX1XSF7Wbpim1wO7pTOaSyfSnT0CxACk2DN10oZcdyXFbT2oY1soZOo4JNOZk7lqHYSonrmDYmBmx24ovAM8eu60Tcl5_C_vj8PBz1JqP6t8bwt8GHQ8tuH7L-8oeFJcxwqf-QnRqMPSJ7js-50yR7ncHp1y_lshaoRxOP5T-yOMuJZO87RlbzlWpMurV4aIfHlHlHo2fkaR7W0I7B6HPS0PMX5HG3qCb4kvwqsUpLrNJFQnOsfrOPAaff6yilFZRSQCnNUUprKM2eUut3TEuM0i1GjykglGYIpTWEviLjfm_UHVh5XRBLMealViS40n6sWCBZHHiCy1iDIeFY-i6SnoYgO7aF9H3GZMBkDDYmiO2kLZXPE1_Y7DVpzhdz_YZQGfFEOIHWEkIJ6BSwtqMSbccsEW4Qxy3CCgmEKifNx9ots9DecutmcgtRbqGRW4tYZa-lIY35S3tRFW6YZpMkMfMjZPd33S-AEOaa6SbEJAnnWEa8RQ6q4ChHg6kQB4MlN9vL0CL2Q5p1838A6TLSt_e_-R15sp3--6SZrtb6PfjvafQhnxV_AOW_8P0
linkProvider Library Specific Holdings
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1ba9swFBZb99C97D6Wrev00Mc42JYlS49dmpJubRishcEYRlcIC0mInYL7U_prpyPbaVN2Y3szWBLW8dG5SEffh9CB4twpm4uIM8ujTFMaqTSWETOZ9gG0MHECt5HPJmx8kX34QrtqwrItq4Qc2jVAEcFWw-KGzeiuJA4IyETuVylUZpFBzgVN6X30gALQCNziiCebgwSvkE0ETAQgMybd7blfjLLlnbawS7ci0J_4qOCPjh8j1c2kKUP5PlhXaqCv7oA8_tdUn6BHbbSKDxv1eoru2fkztDvsSOKeo-tRgKDwngt_ruc-mCynJV44_KlerbxZ_Zr008h9gzoyCYwMU-8pLT7yWn8ZAMdLfDmV-Gi6hAQbD2s9W0CBEyhLGGWrXx8f6kDGZo1_slU9Azvdx35yeOT1bYbfQ23hsl6todELdHE8Oh-Oo5buIdKE0CpSnGmbG02EJEZQzqSx3j4wYDRTklqfO5mEyzwnRAoijTcdwiQuljpnLucJeYl25ou5fYWwVMzxVFgrfYToOwkSp9rZxBDHM2FMD5HuNxe6xUIHSo5ZkdxApga5FyD3opF7D0WbXssGC-QP7fltDSqqsAfjGsKUgvy-616nbUVrVMoCcl_GgB26hw5ua-DmayDDTSEGzsIRdQ8lf9Ns2EoAUBCq1__-0e_Q7vj87LQ4PZl8fIMe-jdZ2KxK99BOtVrbtz58q9R-WKA_ABvUOKA
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1ba9swFBZbB9te1t3KsrWbHvoYBcuyZemxy4XuFgpboTCGkXWBsJCExCl4P6W_tjqynSaju7C9GSwJSz46F-mc70PouBDCFTaTRHArSKLTlBRxpAg3ifYOtDQRhWrkT2N-ep68v0gvtqr4Ia0SYmhXA0UEXQ2be2FcmxEH_GMy85sUErNYLxMyjdO76B6HMlMo4ojGm3sEL4-1A8wkADPStnjuF6PsGKcd6NIdB_QWExXM0WgfqXYidRbK9966LHr6x08Yj_8z08foUeOr4pNauJ6gO3b2FD3otxRxz9DVMABQeLuFP1cz70quJis8d_isWi69Uv1KuzFx3yCLTAEfw8TbSYsHXuYvA9z4Cl9OFB5MFhBe436lp3NIbwJRCaPs9OviEx2o2KzxT7aspqClu9jPDQ-9tE3xW8gsXFTLNTR6js5Hwy_9U9KQPRDNWFqSQnBtM6OZVMzIVHBlrNcOHPjMCpVaHzkZKlSWMaYkU8YrDmmoi5TOuMsEZQdobzaf2RcIq4I7EUtrlfcPfSfJolg7Sw1zIpHGdBBr_3KuGyR0IOSY5vQGMDWsew7rntfr3kFk02tRI4H8ob3YFqC8DCcwrqZLydnvux62wpY3KmWVQ-TLOXBDd9DxtgBuvgbi2xg84CRcUHcQ_Ztm_WYFAAOhfPnvH_0G3T8bjPKP78YfXqGH_kUSTqriQ7RXLtf2yPtuZfE6bM9rMZg3TQ
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=Efficient+Synthesis+of+Pyrrolo%5B1%2C2-f%5Dphenanthridine+Derivatives+via+Dipolar+Cycloaddition+of+Phenanthridine%2C+Activated+Acetylenes%2C+and+Ethyl+Bromopyruvate&rft.jtitle=Synthetic+communications&rft.au=Mehrabi%2C+Hossein&rft.au=Pishahang%2C+Jaleh&rft.date=2014-01-02&rft.pub=Taylor+%26+Francis+Ltd&rft.issn=0039-7911&rft.eissn=1532-2432&rft.volume=44&rft.issue=1&rft.spage=76&rft_id=info:doi/10.1080%2F00397911.2013.789525&rft.externalDBID=NO_FULL_TEXT&rft.externalDocID=3097680121
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0039-7911&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0039-7911&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0039-7911&client=summon