Copper-Catalyzed Tandem CN Bond Formation: An Efficient Annulative Synthesis of Functionalized Cinnolines

Cinn‐tillating synthesis: The combination of a readily available copper catalyst, a simple hydrazide nucleophile, and established difunctionalized building blocks provides a new, flexible route to an under‐developed class of aromatic heterocycles, cinnolines (see scheme).

Saved in:
Bibliographic Details
Published inAngewandte Chemie International Edition Vol. 51; no. 23; pp. 5718 - 5722
Main Authors Ball, Catherine J., Gilmore, Jeremy, Willis, Michael C.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 04.06.2012
WILEY‐VCH Verlag
Wiley
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Cinn‐tillating synthesis: The combination of a readily available copper catalyst, a simple hydrazide nucleophile, and established difunctionalized building blocks provides a new, flexible route to an under‐developed class of aromatic heterocycles, cinnolines (see scheme).
AbstractList Cinn‐tillating synthesis: The combination of a readily available copper catalyst, a simple hydrazide nucleophile, and established difunctionalized building blocks provides a new, flexible route to an under‐developed class of aromatic heterocycles, cinnolines (see scheme).
Author Willis, Michael C.
Gilmore, Jeremy
Ball, Catherine J.
Author_xml – sequence: 1
  givenname: Catherine J.
  surname: Ball
  fullname: Ball, Catherine J.
  organization: Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA (UK) http://mcwillis.chem.ox.ac.uk/MCW/Home.html
– sequence: 2
  givenname: Jeremy
  surname: Gilmore
  fullname: Gilmore, Jeremy
  organization: Lilly Research Centre, Eli Lilly and Company Ltd. Erl Wood Manor, Sunninghill Road, Windlesham, Surrey, GU20 6PH (UK)
– sequence: 3
  givenname: Michael C.
  surname: Willis
  fullname: Willis, Michael C.
  email: michael.willis@chem.ox.ac.uk
  organization: Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA (UK) http://mcwillis.chem.ox.ac.uk/MCW/Home.html
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22539417$$D View this record in MEDLINE/PubMed
BookMark eNqNkt2K1DAUgIusuD9666X0UpCO-WuSejeWmXXZZRZxZcGbkDanGG2T2aZVx9fxQXwkX8HUmR1kQVYI5ITzfcnh5BwnB847SJKnGM0wQuSldhZmBOG4clI8SI7ihjMqBD2IMaM0EzLHh8lxCJ8iLyXij5JDQnJaMCyOkrb06zX0WakH3W6-g0mvtDPQpeWvHz9X6WvvTLr0facH692rdO7SRdPY2oIb4sGNbUx8gfTdxg0fIdiQ-iZdjq6ecN3a6cLSOudb6yA8Th42ug3wZLefJO-Xi6vyTXZxeXpWzi-ymmFeZJBzqGtOZA4VkwLznEtCGpIDNzVHkhNdac0LYTAyxEClmQBpeMGQqShl9CR5vr133fubEcKgOhtqaFvtwI9BYYEwJlRIfD-KsCgkF4JH9NkOHasOjFr3ttP9Rt02MwIvtsBXqHwTpibVsMcQQhQxiRmaIhlp-f90aYc_P1D60Q1RZVu17n0IPTSq3uWHXts2Fq2m4VDTcKj9cERtdke7fe2fQrEr0bawuYdW89XZ4m8327o2DPBt7-r-s-KCilxdr05V-bbg1x_Oz9WK_gYlXtoO
CitedBy_id crossref_primary_10_2174_1570193X15666180712124148
crossref_primary_10_1002_ejoc_202200279
crossref_primary_10_1039_D1QO00945A
crossref_primary_10_1021_acs_orglett_5b03236
crossref_primary_10_1021_acs_joc_0c00275
crossref_primary_10_1039_C5OB01011J
crossref_primary_10_1007_s11164_017_2944_1
crossref_primary_10_1016_j_tet_2017_05_032
crossref_primary_10_1002_ange_201305970
crossref_primary_10_1016_j_tetlet_2022_153984
crossref_primary_10_1002_chem_201300155
crossref_primary_10_1021_acs_orglett_3c00542
crossref_primary_10_1515_gps_2023_0121
crossref_primary_10_1002_chem_201304295
crossref_primary_10_1021_ol5001999
crossref_primary_10_1002_adsc_201700669
crossref_primary_10_1021_acs_orglett_0c00122
crossref_primary_10_1002_ejoc_202101005
crossref_primary_10_1515_psr_2018_0176
crossref_primary_10_1039_D4QO01734J
crossref_primary_10_1002_chem_201300922
crossref_primary_10_1016_j_tetlet_2015_03_134
crossref_primary_10_1055_a_2230_0583
crossref_primary_10_1016_j_dyepig_2017_02_038
crossref_primary_10_1039_C5CC09347C
crossref_primary_10_1002_ajoc_202100588
crossref_primary_10_1002_ejoc_201201386
crossref_primary_10_1016_j_tetlet_2019_04_054
crossref_primary_10_1021_acs_orglett_6b02103
crossref_primary_10_1021_acs_orglett_6b01207
crossref_primary_10_1039_D0CC03789C
crossref_primary_10_1039_D2RA06523A
crossref_primary_10_1002_anie_201204633
crossref_primary_10_1002_anie_201305970
crossref_primary_10_1016_j_tet_2021_131988
crossref_primary_10_1021_acs_joc_4c02525
crossref_primary_10_1021_acs_joc_4c01672
crossref_primary_10_1002_ajoc_202100809
crossref_primary_10_1039_D2QO00144F
crossref_primary_10_1002_adsc_201301009
crossref_primary_10_1039_c3oc90009f
crossref_primary_10_1039_C5QO00331H
crossref_primary_10_1039_C6RA15418B
crossref_primary_10_1021_acs_joc_2c02858
crossref_primary_10_1021_jo5017508
crossref_primary_10_1002_chem_202404479
crossref_primary_10_1039_C7CC03362A
crossref_primary_10_1021_acs_orglett_5b01717
crossref_primary_10_1016_S1872_2067_14_60201_1
crossref_primary_10_1021_jo400071h
crossref_primary_10_1039_C8OB02071J
crossref_primary_10_1021_jo301805d
crossref_primary_10_1002_ange_201204633
crossref_primary_10_1002_chin_201244159
crossref_primary_10_1021_acs_orglett_9b03134
crossref_primary_10_1002_mrm_29166
crossref_primary_10_1016_j_tetlet_2020_152659
crossref_primary_10_1002_adsc_201801221
crossref_primary_10_1039_D3QO00391D
crossref_primary_10_1039_c4cc00374h
crossref_primary_10_1021_acs_joc_6b02062
crossref_primary_10_1039_D2OB00082B
crossref_primary_10_1016_j_bioorg_2020_103932
crossref_primary_10_1515_psr_2021_0091
crossref_primary_10_1021_acs_organomet_0c00800
Cites_doi 10.1021/ol006517x
10.1016/S0040-4039(99)02151-6
10.1016/S0040-4039(99)00949-1
10.1039/C0OB00501K
10.1039/C0SC00331J
10.1016/S0968-0896(02)00604-1
10.1021/cr020095i
10.1039/jr9520002102
10.1016/S0040-4020(00)01141-8
10.1039/jr9500000392
10.1021/cm0340532
10.1021/jo900304a
10.1016/S0040-4020(01)98868-4
10.1016/j.bmcl.2009.11.010
10.1016/j.bmc.2003.10.061
10.1002/adsc.200505484
10.1016/S0968-0896(99)00096-6
10.1016/j.tetlet.2007.08.109
10.1002/1521-4184(200010)333:10<341::AID-ARDP341>3.0.CO;2-U
10.1021/ja8055358
10.1016/j.bmc.2011.03.035
10.1021/ar800036s
10.1002/anie.200602917
10.1002/asia.201100234
10.1039/c1ob05769c
10.1021/ar800098p
10.1002/anie.200800497
10.1021/jm801513z
10.1016/j.bmcl.2006.01.005
10.1002/9780470186558
10.1016/j.tet.2009.08.046
10.1039/j39660002053
10.3987/R-1976-01-0035
10.1002/ange.200602917
10.1021/cr050041j
10.1002/ange.200461598
10.1016/S0040-4039(03)00686-5
10.1002/anie.200461598
10.1016/S0960-894X(02)00737-0
10.1016/0040-4039(95)00005-W
10.1021/ol0168216
10.1016/j.bmc.2006.06.047
10.1016/j.jorganchem.2010.06.017
10.1016/S0040-4020(00)00448-8
10.3987/COM-08-S(F)7
10.1002/ange.200800497
10.1002/ardp.200500194
10.1021/ja01541a050
10.1016/j.bmcl.2011.01.033
10.1039/c0sc00107d
10.1021/ja016226z
10.1002/cber.188301601154
10.1021/ol062978s
10.1021/ol802624e
10.1016/j.tet.2010.05.046
10.1039/c0ob00501k
10.1055/s-0030-1258294
10.1039/c0sc00331j
ContentType Journal Article
Copyright Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
Copyright_xml – notice: Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
DBID BSCLL
AAYXX
CITATION
17B
1KM
1KN
BLEPL
DTL
EGQ
GKHJH
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7SR
8BQ
8FD
JG9
DOI 10.1002/anie.201201529
DatabaseName Istex
CrossRef
Web of Knowledge
Index Chemicus
Current Chemical Reactions
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
Web of Science - Science Citation Index Expanded - 2012
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
Engineered Materials Abstracts
METADEX
Technology Research Database
Materials Research Database
DatabaseTitle CrossRef
Web of Science
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
Materials Research Database
Engineered Materials Abstracts
Technology Research Database
METADEX
DatabaseTitleList
Materials Research Database
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: 1KN
  name: Current Chemical Reactions
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1521-3773
EndPage 5722
ExternalDocumentID 22539417
000304814000038
10_1002_anie_201201529
ANIE201201529
ark_67375_WNG_CQ96WZKK_N
Genre shortCommunication
Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: Eli Lilly
– fundername: EPSRC
– fundername: EPSRC; UK Research & Innovation (UKRI); Engineering & Physical Sciences Research Council (EPSRC)
GroupedDBID ---
-DZ
-~X
.3N
.GA
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
23M
31~
33P
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52S
52T
52U
52W
52X
53G
5GY
5RE
5VS
66C
6TJ
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A03
AAESR
AAEVG
AAHHS
AANLZ
AAONW
AASGY
AAXRX
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABLJU
ABPPZ
ABPVW
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACFBH
ACGFS
ACIWK
ACNCT
ACPOU
ACPRK
ACSCC
ACXBN
ACXQS
ADBBV
ADEOM
ADIZJ
ADKYN
ADMGS
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEIGN
AEIMD
AEQDE
AEUQT
AEUYR
AFBPY
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFZJQ
AHBTC
AHMBA
AITYG
AIURR
AIWBW
AJBDE
AJXKR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMBMR
AMYDB
ATUGU
AUFTA
AZBYB
AZFZN
AZVAB
B-7
BAFTC
BDRZF
BFHJK
BHBCM
BMNLL
BMXJE
BNHUX
BROTX
BRXPI
BSCLL
BTSUX
BY8
CS3
D-E
D-F
D0L
DCZOG
DPXWK
DR1
DR2
DRFUL
DRSTM
EBS
EJD
F00
F01
F04
F5P
FEDTE
G-S
G.N
GNP
GODZA
H.T
H.X
HBH
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M53
MEWTI
MK4
MRFUL
MRSTM
MSFUL
MSSTM
MXFUL
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
P2P
P2W
P2X
P4D
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RNS
ROL
RWI
RX1
RYL
SUPJJ
TN5
UB1
UPT
V2E
VQA
W8V
W99
WBFHL
WBKPD
WH7
WIB
WIH
WIK
WJL
WOHZO
WQJ
WRC
WXSBR
WYISQ
XG1
XPP
XSW
XV2
YZZ
ZZTAW
~IA
~KM
~WT
AAHQN
AAMNL
AANHP
AAYCA
ACRPL
ACYXJ
ADNMO
AFWVQ
ALVPJ
AAYXX
ABDBF
ABJNI
AETEA
AEYWJ
AGQPQ
AGYGG
CITATION
17B
1KM
1KN
BLEPL
DTL
GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED
GROUPED_WOS_WEB_OF_SCIENCE
CGR
CUY
CVF
ECM
EIF
NPM
7X8
7SR
8BQ
8FD
JG9
ID FETCH-LOGICAL-c4169-e56ecc6285eb4871656822f25e6dc60862abaa697d10d2deba47e8d6940db3343
IEDL.DBID DR2
ISICitedReferencesCount 71
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000304814000038
ISSN 1433-7851
1521-3773
IngestDate Thu Jul 10 18:06:05 EDT 2025
Fri Jul 11 15:15:15 EDT 2025
Mon Jul 21 06:00:57 EDT 2025
Fri Aug 29 16:21:09 EDT 2025
Wed Jul 09 15:26:27 EDT 2025
Thu Apr 24 23:00:07 EDT 2025
Tue Jul 01 02:52:58 EDT 2025
Wed Jan 22 17:01:44 EST 2025
Wed Oct 30 09:55:49 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 23
Keywords ROUTE
cinnolines
NITROGEN-HETEROCYCLES
ANTICANCER AGENTS
copper catalysis
tandem processes
AMINATION
annulation
FACILE SYNTHESIS
LIGANDS
heterocycles
ALKENYL
ANTIFUNGAL
DERIVATIVES
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
LinkModel DirectLink
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c4169-e56ecc6285eb4871656822f25e6dc60862abaa697d10d2deba47e8d6940db3343
Notes EPSRC
This work was supported by the EPSRC and Eli Lilly.
Eli Lilly
ark:/67375/WNG-CQ96WZKK-N
istex:F4C9A1D49AE43197D7CC4B968CAD032F16D477AB
ArticleID:ANIE201201529
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 22539417
PQID 1017986776
PQPubID 23479
PageCount 5
ParticipantIDs webofscience_primary_000304814000038
pubmed_primary_22539417
proquest_miscellaneous_1017986776
crossref_citationtrail_10_1002_anie_201201529
proquest_miscellaneous_1701123781
webofscience_primary_000304814000038CitationCount
wiley_primary_10_1002_anie_201201529_ANIE201201529
crossref_primary_10_1002_anie_201201529
istex_primary_ark_67375_WNG_CQ96WZKK_N
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate June 4, 2012
PublicationDateYYYYMMDD 2012-06-04
PublicationDate_xml – month: 06
  year: 2012
  text: June 4, 2012
  day: 04
PublicationDecade 2010
PublicationPlace Weinheim
PublicationPlace_xml – name: Weinheim
– name: WEINHEIM
– name: Germany
PublicationTitle Angewandte Chemie International Edition
PublicationTitleAbbrev ANGEW CHEM INT EDIT
PublicationTitleAlternate Angew. Chem. Int. Ed
PublicationYear 2012
Publisher WILEY-VCH Verlag
WILEY‐VCH Verlag
Wiley
Publisher_xml – name: WILEY-VCH Verlag
– name: WILEY‐VCH Verlag
– name: Wiley
References For the use of a related alkenyl triflate substrate, see: M. C. Willis, G. N. Brace, I. P. Holmes, Angew. Chem. 2005, 117, 407
W. R. Pitt, D. M. Parry, B. D. Perry, C. R. Groom, J. Med. Chem. 2009, 52, 2952.
Y. N. Yu, S. K. Singh, A. Liu, T. K. Li, L. F. Liu, E. J. LaVoie, Bioorg. Med. Chem. 2003, 11, 1475
Angew. Chem. Int. Ed. 2006, 45, 7079
J. C. E. Simpson, The Chemistry of Heterocyclic Compounds, Condensed Pyridazine and Pyrazine Rings, Cinnolines, Phthalazines and Quinoxalines, Vol. 5, Wiley, New York, 1953.
S. W. Schneller, P. N. Skancke, Heterocycles 1976, 4, 35
J. E. R. Sadig, M. C. Willis, Synthesis 2011, 1-22
D. A. Scott, L. A. Dakin, D. J. Del Valle, R. B. Diebold, L. Drew, T. W. Gero, C. A. Ogoe, C. A. Omer, G. Repik, K. Thakur, Q. Ye, X. Zheng, Bioorg. Med. Chem. Lett. 2011, 21, 1382.
V. G. Chapoulaud, N. Plé, A. Turck, G. Quéguiner, Tetrahedron 2000, 56, 5499
A. Klapars, J. C. Antilla, X. H. Huang, S. L. Buchwald, J. Am. Chem. Soc. 2001, 123, 7727
K. W. Woods, J. P. Fischer, A. Claiborne, T. Li, S. A. Thomas, G.-D. Zhu, R. B. Diebold, X. Liu, Y. Shi, V. Klinghofer, E. K. Han, R. Guan, S. R. Magnone, E. F. Johnson, J. J. Bouska, A. M. Olson, R. de Jong, T. Oltersdorf, Y. Luo, S. H. Rosenberg, V. L. Giranda, Q. Li, Bioorg. Med. Chem. 2006, 14, 6832
E. J. Alford, K. Schofield, J. Chem. Soc. 1952, 2102
H. E. Baumgarten, C. H. Anderson, J. Am. Chem. Soc. 1958, 80, 1981
D. S. Surry, S. L. Buchwald, Chem. Sci. 2011, 2, 27.
M. Alajarin, B. Bonillo, M. Marin-Luna, A. Vidal, R.-A. Orenes, J. Org. Chem. 2009, 74, 3558.
C. K. Ryu, J. Y. Lee, Bioorg. Med. Chem. Lett. 2006, 16, 1850.
P. Barraja, P. Diana, A. Lauria, A. Passannanti, A. M. Almerico, C. Minnei, S. Longu, D. Congiu, C. Musiu, P. La Colla, Bioorg. Med. Chem. 1999, 7, 1591
A. S. Kiselyov, Tetrahedron Lett. 1995, 36, 1383
I. Nakamura, Y. Yamamoto, Chem. Rev. 2004, 104, 2127.
C. B. Kanner, U. K. Pandit, Tetrahedron 1981, 37, 3513
A. C. Tadd, M. R. Fielding, M. C. Willis, Tetrahedron Lett. 2007, 48, 7578.
S. Cacchi, G. Fabrizi, A. Goggiamani, Org. Biomol. Chem. 2011, 9, 641
C. Alhambra, C. Becker, T. Blake, A. Chang, J. R. Damewood Jr., T. Daniels, B. T. Dembofsky, D. A. Gurley, J. E. Hall, K. J. Herzog, C. L. Horchler, C. J. Ohnmacht, R. J. Schmiesing, A. Dudley, M. D. Ribadeneira, K. S. Knappenberger, C. Maciag, M. M. Stein, M. Chopra, X. F. Liu, E. P. Christian, J. L. Arriza, M. Chapdelaine, Bioorg. Med. Chem. 2011, 19, 2927.
A. S. Kiselyov, C. Dominguez, Tetrahedron Lett. 1999, 40, 5111.
M. S. Shvartsberg, I. D. Ivanchikova, Tetrahedron Lett. 2000, 41, 771
T. Mitsumori, M. Bendikov, J. Sedo, F. Wudl, Chem. Mater. 2003, 15, 3759
D. S. Surry, S. L. Buchwald, Angew. Chem. 2008, 120, 6438
J. F. Hartwig, Acc. Chem. Res. 2008, 41, 1534.
M. Wolter, A. Klapars, S. L. Buchwald, Org. Lett. 2001, 3, 3803
E. Gavini, C. Juliano, A. Mule, G. Pirisino, G. Murineddu, G. A. Pinna, Arch. Pharm. 2000, 333, 341
L. C. Henderson, M. J. Lindon, M. C. Willis, Tetrahedron 2010, 66, 6632
Y. Liu, J.-P. Wan, Org. Biomol. Chem. 2011, 9, 6873
R. Martín, M. R. Rivero, S. L. Buchwald, Angew. Chem. 2006, 118, 7237
C. M. Atkinson, B. N. Biddle, J. Chem. Soc. C 1966, 2053.
M. R. Rivero, S. L. Buchwald, Org. Lett. 2007, 9, 973.
B. P. Fors, D. A. Watson, M. R. Biscoe, S. L. Buchwald, J. Am. Chem. Soc. 2008, 130, 13552.
M. C. Willis, G. N. Brace, T. J. K. Findlay, I. P. Holmes, Adv. Synth. Catal. 2006, 348, 851
W. Lewgowd, A. Stanczak, Arch. Pharm. 2007, 340, 65
M. A. M. Gomaa, Tetrahedron Lett. 2003, 44, 3493
D. Chen, C. Yang, Y. Xie, J. Ding, Heterocycles 2009, 77, 273
Angew. Chem. Int. Ed. 2008, 47, 6338
K. Schofield, T. Swain, J. Chem. Soc. 1950, 392.
N. T. Patil, Y. Yamamoto, Chem. Rev. 2008, 108, 3395
H. Tsuji, Y. Yokoi, Y. Sato, H. Tanaka, E. Nakamura, Chem. Asian J. 2011, 6, 2005.
A. L. Ruchelman, S. K. Singh, X. H. Wu, A. Ray, J. M. Yang, T. K. Li, A. Liu, L. F. Liu, E. J. LaVoie, Bioorg. Med. Chem. Lett. 2002, 12, 3333.
A. L. Ruchelman, S. K. Singh, A. Ray, X. H. Wu, J. M. Yang, N. Zhou, A. Liu, L. F. Liu, E. J. LaVoie, Bioorg. Med. Chem. 2004, 12, 795
C. Lunniss, C. Eldred, N. Aston, A. Craven, K. Gohil, B. Judkins, S. Keeling, L. Ranshaw, E. Robinson, T. Shipley, N. Trivedi, Bioorg. Med. Chem. Lett. 2010, 20, 137.
for a AuI-catalyzed approach to dihydrocinnolines, see: I. D. Jurberg, F. Gagosz, J. Organomet. Chem. 2011, 696, 37.
R. C. Hodgkinson, J. Schulz, M. C. Willis, Tetrahedron 2009, 65, 8940
Angew. Chem. Int. Ed. 2005, 44, 403.
V. von Richter, Chem. Ber. 1883, 16, 677
R. Martin, S. L. Buchwald, Acc. Chem. Res. 2008, 41, 1461.
For the use of triazenes to access related intermediates, see: D. B. Kimball, A. G. Hayes, M. M. Haley, Org. Lett. 2000, 2, 3825.
A. C. Tadd, A. Matsuno, M. R. Fielding, M. C. Willis, Org. Lett. 2009, 11, 583.
N. A. Al-Awadi, M. H. Elnagdi, Y. Ibrahim, K. Kaul, A. Kumar, Tetrahedron 2001, 57, 1609
D. S. Surry, S. L. Buchwald, Chem. Sci. 2010, 1, 13
2000; 333
1995; 36
2002; 12
2000; 41
2007; 340
2008; 108
2003; 15
2000; 2
1999; 40
2011; 19
2006 2006; 118 45
2003; 11
2010; 66
2009; 11
2010; 20
2009; 52
2010; 1
2000; 56
2007; 9
2011; 21
1981; 37
1958; 80
2001; 57
2003; 44
2005 2005; 117 44
2011; 696
2001; 123
2004; 104
2009; 65
2011; 2
2011
2006; 16
2006; 14
1953
1952
1950
1999; 7
2011; 6
1976; 4
2011; 9
2009; 77
1883; 16
2009; 74
2004; 12
2001; 3
2008; 41
2008 2008; 120 47
2006; 348
2008; 130
2007; 48
1966
e_1_2_2_2_3
e_1_2_2_24_2
e_1_2_2_47_2
e_1_2_2_4_2
e_1_2_2_22_2
e_1_2_2_49_2
e_1_2_2_6_2
e_1_2_2_20_2
e_1_2_2_2_2
e_1_2_2_62_2
Simpson J. C. E. (e_1_2_2_25_2) 1953
e_1_2_2_41_2
e_1_2_2_64_2
e_1_2_2_8_2
e_1_2_2_28_2
e_1_2_2_43_2
e_1_2_2_66_2
e_1_2_2_26_2
e_1_2_2_45_2
e_1_2_2_68_2
e_1_2_2_60_2
e_1_2_2_13_2
e_1_2_2_36_2
e_1_2_2_59_2
e_1_2_2_11_2
e_1_2_2_38_2
e_1_2_2_51_2
e_1_2_2_19_2
e_1_2_2_30_2
e_1_2_2_53_2
e_1_2_2_51_3
e_1_2_2_17_2
e_1_2_2_32_2
e_1_2_2_55_2
e_1_2_2_15_2
e_1_2_2_34_2
e_1_2_2_57_2
e_1_2_2_3_2
e_1_2_2_23_2
e_1_2_2_48_2
e_1_2_2_21_2
e_1_2_2_1_2
e_1_2_2_40_2
e_1_2_2_61_2
e_1_2_2_29_2
e_1_2_2_42_2
e_1_2_2_63_2
e_1_2_2_7_2
e_1_2_2_27_2
e_1_2_2_44_2
e_1_2_2_65_2
e_1_2_2_9_2
e_1_2_2_46_2
e_1_2_2_67_2
e_1_2_2_58_3
e_1_2_2_12_2
e_1_2_2_37_2
e_1_2_2_58_2
e_1_2_2_10_2
e_1_2_2_39_2
e_1_2_2_50_2
e_1_2_2_18_2
e_1_2_2_31_2
e_1_2_2_52_2
e_1_2_2_16_2
e_1_2_2_33_2
e_1_2_2_54_2
e_1_2_2_14_2
e_1_2_2_35_2
e_1_2_2_56_2
Sadig J. E. R. (e_1_2_2_5_2) 2011
Martin, R (WOS:000261000000005) 2008; 41
Shvartsberg, MS (WOS:000085038700045) 2000; 41
Surry, DS (WOS:000258584800004) 2008; 47
Jurberg, ID (WOS:000285918100005) 2011; 696
von Richter, V. (000304814000038.50) 1883; 16
Surry, D. S. (000304814000038.44) 2008; 120
Alajarin, M (WOS:000265554900048) 2009; 74
Simpson, J. C. E. (000304814000038.42) 1953; 5
Alhambra, C (WOS:000289834600016) 2011; 19
Ruchelman, AL (WOS:000178916300022) 2002; 12
Tadd, AC (WOS:000250310800004) 2007; 48
Hodgkinson, RC (WOS:000271345600005) 2009; 65
Surry, DS (WOS:000285009500003) 2011; 2
Fors, BP (WOS:000259924000022) 2008; 130
Woods, KW (WOS:000241227400005) 2006; 14
Tadd, AC (WOS:000262913500022) 2009; 11
Al-Awadi, NA (WOS:000167054100020) 2001; 57
Mitsumori, T (WOS:000185747100007) 2003; 15
Sadig, JER (WOS:000286506800004) 2011
ATKINSON, CM (WOS:A19668520600011) 1966
Hartwig, JF (WOS:000261000000012) 2008; 41
BAUMGARTEN, HE (WOS:A1958WB38300050) 1958; 80
Yu, YN (WOS:000181715100032) 2003; 11
ALFORD, EJ (WOS:A1952UB67400022) 1952
Barraja, P (WOS:000082137500012) 1999; 7
Rivero, MR (WOS:000244735900007) 2007; 9
Cacchi, S (WOS:000286431500001) 2011; 9
SCHOFIELD, K (WOS:A1950UB59000086) 1950
Lunniss, C (WOS:000272935600027) 2010; 20
Martin, R. (000304814000038.26) 2006; 118
SCHNELLER, SW (WOS:A1976BA45700007) 1976; 4
Gavini, E (WOS:000165128800005) 2000; 333
Henderson, LC (WOS:000280902200040) 2010; 66
Ryu, CK (WOS:000236402500017) 2006; 16
KISELYOV, AS (WOS:A1995QK51800001) 1995; 36
Willis, MC (WOS:000237745100011) 2006; 348
Liu, YY (WOS:000295889900001) 2011; 9
Chapoulaud, VG (WOS:000088275700025) 2000; 56
Scott, DA (WOS:000287440000019) 2011; 21
Klapars, A (WOS:000170299800042) 2001; 123
Willis, M. C. (000304814000038.52) 2005; 117
Wolter, M (WOS:000172181700051) 2001; 3
Kiselyov, AS (WOS:000081250300003) 1999; 40
Chen, DD (WOS:000263374600025) 2009; 77
Lewgowd, W (WOS:000244909700001) 2007; 340
Patil, NT (WOS:000259077600024) 2008; 108
Tsuji, H (WOS:000294112200021) 2011; 6
Ruchelman, AL (WOS:000188964600015) 2004; 12
Nakamura, I (WOS:000221418500002) 2004; 104
Gomaa, MAM (WOS:000182267000013) 2003; 44
Willis, MC (WOS:000226425600008) 2005; 44
Pitt, WR (WOS:000265911800033) 2009; 52
Martin, R (WOS:000241976300034) 2006; 45
KANNER, CB (WOS:A1981MM18400011) 1981; 37
Kimball, DB (WOS:000165616300018) 2000; 2
Surry, DS (WOS:000281247900002) 2010; 1
References_xml – reference: for a AuI-catalyzed approach to dihydrocinnolines, see: I. D. Jurberg, F. Gagosz, J. Organomet. Chem. 2011, 696, 37.
– reference: J. E. R. Sadig, M. C. Willis, Synthesis 2011, 1-22;
– reference: E. Gavini, C. Juliano, A. Mule, G. Pirisino, G. Murineddu, G. A. Pinna, Arch. Pharm. 2000, 333, 341;
– reference: Angew. Chem. Int. Ed. 2006, 45, 7079;
– reference: S. Cacchi, G. Fabrizi, A. Goggiamani, Org. Biomol. Chem. 2011, 9, 641;
– reference: C. Lunniss, C. Eldred, N. Aston, A. Craven, K. Gohil, B. Judkins, S. Keeling, L. Ranshaw, E. Robinson, T. Shipley, N. Trivedi, Bioorg. Med. Chem. Lett. 2010, 20, 137.
– reference: C. M. Atkinson, B. N. Biddle, J. Chem. Soc. C 1966, 2053.
– reference: N. T. Patil, Y. Yamamoto, Chem. Rev. 2008, 108, 3395;
– reference: K. W. Woods, J. P. Fischer, A. Claiborne, T. Li, S. A. Thomas, G.-D. Zhu, R. B. Diebold, X. Liu, Y. Shi, V. Klinghofer, E. K. Han, R. Guan, S. R. Magnone, E. F. Johnson, J. J. Bouska, A. M. Olson, R. de Jong, T. Oltersdorf, Y. Luo, S. H. Rosenberg, V. L. Giranda, Q. Li, Bioorg. Med. Chem. 2006, 14, 6832;
– reference: A. S. Kiselyov, C. Dominguez, Tetrahedron Lett. 1999, 40, 5111.
– reference: M. C. Willis, G. N. Brace, T. J. K. Findlay, I. P. Holmes, Adv. Synth. Catal. 2006, 348, 851;
– reference: C. B. Kanner, U. K. Pandit, Tetrahedron 1981, 37, 3513;
– reference: D. S. Surry, S. L. Buchwald, Angew. Chem. 2008, 120, 6438;
– reference: A. C. Tadd, A. Matsuno, M. R. Fielding, M. C. Willis, Org. Lett. 2009, 11, 583.
– reference: For the use of triazenes to access related intermediates, see: D. B. Kimball, A. G. Hayes, M. M. Haley, Org. Lett. 2000, 2, 3825.
– reference: D. Chen, C. Yang, Y. Xie, J. Ding, Heterocycles 2009, 77, 273;
– reference: A. Klapars, J. C. Antilla, X. H. Huang, S. L. Buchwald, J. Am. Chem. Soc. 2001, 123, 7727;
– reference: M. Wolter, A. Klapars, S. L. Buchwald, Org. Lett. 2001, 3, 3803;
– reference: V. G. Chapoulaud, N. Plé, A. Turck, G. Quéguiner, Tetrahedron 2000, 56, 5499;
– reference: C. K. Ryu, J. Y. Lee, Bioorg. Med. Chem. Lett. 2006, 16, 1850.
– reference: Angew. Chem. Int. Ed. 2008, 47, 6338;
– reference: L. C. Henderson, M. J. Lindon, M. C. Willis, Tetrahedron 2010, 66, 6632;
– reference: J. C. E. Simpson, The Chemistry of Heterocyclic Compounds, Condensed Pyridazine and Pyrazine Rings, Cinnolines, Phthalazines and Quinoxalines, Vol. 5, Wiley, New York, 1953.
– reference: R. Martin, S. L. Buchwald, Acc. Chem. Res. 2008, 41, 1461.
– reference: W. R. Pitt, D. M. Parry, B. D. Perry, C. R. Groom, J. Med. Chem. 2009, 52, 2952.
– reference: A. L. Ruchelman, S. K. Singh, A. Ray, X. H. Wu, J. M. Yang, N. Zhou, A. Liu, L. F. Liu, E. J. LaVoie, Bioorg. Med. Chem. 2004, 12, 795;
– reference: P. Barraja, P. Diana, A. Lauria, A. Passannanti, A. M. Almerico, C. Minnei, S. Longu, D. Congiu, C. Musiu, P. La Colla, Bioorg. Med. Chem. 1999, 7, 1591;
– reference: T. Mitsumori, M. Bendikov, J. Sedo, F. Wudl, Chem. Mater. 2003, 15, 3759;
– reference: J. F. Hartwig, Acc. Chem. Res. 2008, 41, 1534.
– reference: R. C. Hodgkinson, J. Schulz, M. C. Willis, Tetrahedron 2009, 65, 8940;
– reference: M. S. Shvartsberg, I. D. Ivanchikova, Tetrahedron Lett. 2000, 41, 771;
– reference: B. P. Fors, D. A. Watson, M. R. Biscoe, S. L. Buchwald, J. Am. Chem. Soc. 2008, 130, 13552.
– reference: S. W. Schneller, P. N. Skancke, Heterocycles 1976, 4, 35;
– reference: W. Lewgowd, A. Stanczak, Arch. Pharm. 2007, 340, 65;
– reference: E. J. Alford, K. Schofield, J. Chem. Soc. 1952, 2102;
– reference: A. C. Tadd, M. R. Fielding, M. C. Willis, Tetrahedron Lett. 2007, 48, 7578.
– reference: C. Alhambra, C. Becker, T. Blake, A. Chang, J. R. Damewood Jr., T. Daniels, B. T. Dembofsky, D. A. Gurley, J. E. Hall, K. J. Herzog, C. L. Horchler, C. J. Ohnmacht, R. J. Schmiesing, A. Dudley, M. D. Ribadeneira, K. S. Knappenberger, C. Maciag, M. M. Stein, M. Chopra, X. F. Liu, E. P. Christian, J. L. Arriza, M. Chapdelaine, Bioorg. Med. Chem. 2011, 19, 2927.
– reference: A. L. Ruchelman, S. K. Singh, X. H. Wu, A. Ray, J. M. Yang, T. K. Li, A. Liu, L. F. Liu, E. J. LaVoie, Bioorg. Med. Chem. Lett. 2002, 12, 3333.
– reference: M. Alajarin, B. Bonillo, M. Marin-Luna, A. Vidal, R.-A. Orenes, J. Org. Chem. 2009, 74, 3558.
– reference: H. Tsuji, Y. Yokoi, Y. Sato, H. Tanaka, E. Nakamura, Chem. Asian J. 2011, 6, 2005.
– reference: V. von Richter, Chem. Ber. 1883, 16, 677;
– reference: M. R. Rivero, S. L. Buchwald, Org. Lett. 2007, 9, 973.
– reference: Y. Liu, J.-P. Wan, Org. Biomol. Chem. 2011, 9, 6873;
– reference: Y. N. Yu, S. K. Singh, A. Liu, T. K. Li, L. F. Liu, E. J. LaVoie, Bioorg. Med. Chem. 2003, 11, 1475;
– reference: K. Schofield, T. Swain, J. Chem. Soc. 1950, 392.
– reference: H. E. Baumgarten, C. H. Anderson, J. Am. Chem. Soc. 1958, 80, 1981;
– reference: M. A. M. Gomaa, Tetrahedron Lett. 2003, 44, 3493;
– reference: D. S. Surry, S. L. Buchwald, Chem. Sci. 2010, 1, 13;
– reference: I. Nakamura, Y. Yamamoto, Chem. Rev. 2004, 104, 2127.
– reference: For the use of a related alkenyl triflate substrate, see: M. C. Willis, G. N. Brace, I. P. Holmes, Angew. Chem. 2005, 117, 407;
– reference: D. A. Scott, L. A. Dakin, D. J. Del Valle, R. B. Diebold, L. Drew, T. W. Gero, C. A. Ogoe, C. A. Omer, G. Repik, K. Thakur, Q. Ye, X. Zheng, Bioorg. Med. Chem. Lett. 2011, 21, 1382.
– reference: A. S. Kiselyov, Tetrahedron Lett. 1995, 36, 1383;
– reference: N. A. Al-Awadi, M. H. Elnagdi, Y. Ibrahim, K. Kaul, A. Kumar, Tetrahedron 2001, 57, 1609;
– reference: Angew. Chem. Int. Ed. 2005, 44, 403.
– reference: D. S. Surry, S. L. Buchwald, Chem. Sci. 2011, 2, 27.
– reference: R. Martín, M. R. Rivero, S. L. Buchwald, Angew. Chem. 2006, 118, 7237;
– volume: 340
  start-page: 65
  year: 2007
  publication-title: Arch. Pharm.
– volume: 56
  start-page: 5499
  year: 2000
  publication-title: Tetrahedron
– volume: 3
  start-page: 3803
  year: 2001
  publication-title: Org. Lett.
– volume: 40
  start-page: 5111
  year: 1999
  publication-title: Tetrahedron Lett.
– volume: 19
  start-page: 2927
  year: 2011
  publication-title: Bioorg. Med. Chem.
– volume: 9
  start-page: 973
  year: 2007
  publication-title: Org. Lett.
– start-page: 1
  year: 2011
  end-page: 22
  publication-title: Synthesis
– volume: 6
  start-page: 2005
  year: 2011
  publication-title: Chem. Asian J.
– volume: 118 45
  start-page: 7237 7079
  year: 2006 2006
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 104
  start-page: 2127
  year: 2004
  publication-title: Chem. Rev.
– volume: 20
  start-page: 137
  year: 2010
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 7
  start-page: 1591
  year: 1999
  publication-title: Bioorg. Med. Chem.
– volume: 65
  start-page: 8940
  year: 2009
  publication-title: Tetrahedron
– start-page: 392
  year: 1950
  publication-title: J. Chem. Soc.
– volume: 333
  start-page: 341
  year: 2000
  publication-title: Arch. Pharm.
– volume: 36
  start-page: 1383
  year: 1995
  publication-title: Tetrahedron Lett.
– volume: 130
  start-page: 13552
  year: 2008
  publication-title: J. Am. Chem. Soc.
– start-page: 2102
  year: 1952
  publication-title: J. Chem. Soc.
– volume: 9
  start-page: 6873
  year: 2011
  publication-title: Org. Biomol. Chem.
– volume: 44
  start-page: 3493
  year: 2003
  publication-title: Tetrahedron Lett.
– volume: 1
  start-page: 13
  year: 2010
  publication-title: Chem. Sci.
– volume: 21
  start-page: 1382
  year: 2011
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 77
  start-page: 273
  year: 2009
  publication-title: Heterocycles
– volume: 108
  start-page: 3395
  year: 2008
  publication-title: Chem. Rev.
– volume: 11
  start-page: 1475
  year: 2003
  publication-title: Bioorg. Med. Chem.
– volume: 37
  start-page: 3513
  year: 1981
  publication-title: Tetrahedron
– volume: 48
  start-page: 7578
  year: 2007
  publication-title: Tetrahedron Lett.
– volume: 120 47
  start-page: 6438 6338
  year: 2008 2008
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 4
  start-page: 35
  year: 1976
  publication-title: Heterocycles
– volume: 41
  start-page: 1534
  year: 2008
  publication-title: Acc. Chem. Res.
– volume: 15
  start-page: 3759
  year: 2003
  publication-title: Chem. Mater.
– volume: 9
  start-page: 641
  year: 2011
  publication-title: Org. Biomol. Chem.
– volume: 12
  start-page: 795
  year: 2004
  publication-title: Bioorg. Med. Chem.
– volume: 57
  start-page: 1609
  year: 2001
  publication-title: Tetrahedron
– volume: 41
  start-page: 1461
  year: 2008
  publication-title: Acc. Chem. Res.
– volume: 117 44
  start-page: 407 403
  year: 2005 2005
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 74
  start-page: 3558
  year: 2009
  publication-title: J. Org. Chem.
– volume: 348
  start-page: 851
  year: 2006
  publication-title: Adv. Synth. Catal.
– volume: 123
  start-page: 7727
  year: 2001
  publication-title: J. Am. Chem. Soc.
– volume: 696
  start-page: 37
  year: 2011
  publication-title: J. Organomet. Chem.
– volume: 16
  start-page: 1850
  year: 2006
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 2
  start-page: 27
  year: 2011
  publication-title: Chem. Sci.
– start-page: 2053
  year: 1966
  publication-title: J. Chem. Soc. C
– volume: 80
  start-page: 1981
  year: 1958
  publication-title: J. Am. Chem. Soc.
– volume: 16
  start-page: 677
  year: 1883
  publication-title: Chem. Ber.
– volume: 2
  start-page: 3825
  year: 2000
  publication-title: Org. Lett.
– volume: 12
  start-page: 3333
  year: 2002
  publication-title: Bioorg. Med. Chem. Lett.
– volume: 41
  start-page: 771
  year: 2000
  publication-title: Tetrahedron Lett.
– volume: 66
  start-page: 6632
  year: 2010
  publication-title: Tetrahedron
– volume: 14
  start-page: 6832
  year: 2006
  publication-title: Bioorg. Med. Chem.
– year: 1953
– volume: 52
  start-page: 2952
  year: 2009
  publication-title: J. Med. Chem.
– volume: 11
  start-page: 583
  year: 2009
  publication-title: Org. Lett.
– ident: e_1_2_2_28_2
  doi: 10.1021/ol006517x
– ident: e_1_2_2_35_2
  doi: 10.1016/S0040-4039(99)02151-6
– ident: e_1_2_2_39_2
  doi: 10.1016/S0040-4039(99)00949-1
– ident: e_1_2_2_61_2
– ident: e_1_2_2_7_2
  doi: 10.1039/C0OB00501K
– ident: e_1_2_2_68_2
  doi: 10.1039/C0SC00331J
– ident: e_1_2_2_12_2
  doi: 10.1016/S0968-0896(02)00604-1
– ident: e_1_2_2_9_2
  doi: 10.1021/cr020095i
– ident: e_1_2_2_41_2
  doi: 10.1039/jr9520002102
– ident: e_1_2_2_36_2
  doi: 10.1016/S0040-4020(00)01141-8
– ident: e_1_2_2_31_2
  doi: 10.1039/jr9500000392
– ident: e_1_2_2_21_2
  doi: 10.1021/cm0340532
– ident: e_1_2_2_46_2
  doi: 10.1021/jo900304a
– ident: e_1_2_2_34_2
  doi: 10.1016/S0040-4020(01)98868-4
– ident: e_1_2_2_60_2
– ident: e_1_2_2_19_2
  doi: 10.1016/j.bmcl.2009.11.010
– ident: e_1_2_2_13_2
  doi: 10.1016/j.bmc.2003.10.061
– ident: e_1_2_2_48_2
  doi: 10.1002/adsc.200505484
– ident: e_1_2_2_16_2
  doi: 10.1016/S0968-0896(99)00096-6
– ident: e_1_2_2_53_2
  doi: 10.1016/j.tetlet.2007.08.109
– ident: e_1_2_2_17_2
  doi: 10.1002/1521-4184(200010)333:10<341::AID-ARDP341>3.0.CO;2-U
– ident: e_1_2_2_67_2
  doi: 10.1021/ja8055358
– start-page: 1
  year: 2011
  ident: e_1_2_2_5_2
  publication-title: Synthesis
– ident: e_1_2_2_43_2
– ident: e_1_2_2_45_2
  doi: 10.1016/j.bmc.2011.03.035
– ident: e_1_2_2_62_2
  doi: 10.1021/ar800036s
– ident: e_1_2_2_32_2
– ident: e_1_2_2_58_3
  doi: 10.1002/anie.200602917
– ident: e_1_2_2_23_2
  doi: 10.1002/asia.201100234
– ident: e_1_2_2_6_2
  doi: 10.1039/c1ob05769c
– ident: e_1_2_2_40_2
– ident: e_1_2_2_54_2
– ident: e_1_2_2_3_2
  doi: 10.1021/ar800098p
– ident: e_1_2_2_2_3
  doi: 10.1002/anie.200800497
– ident: e_1_2_2_66_2
  doi: 10.1021/jm801513z
– ident: e_1_2_2_18_2
  doi: 10.1016/j.bmcl.2006.01.005
– volume-title: The Chemistry of Heterocyclic Compounds, Condensed Pyridazine and Pyrazine Rings, Cinnolines, Phthalazines and Quinoxalines, Vol. 5
  year: 1953
  ident: e_1_2_2_25_2
  doi: 10.1002/9780470186558
– ident: e_1_2_2_50_2
  doi: 10.1016/j.tet.2009.08.046
– ident: e_1_2_2_63_2
  doi: 10.1039/j39660002053
– ident: e_1_2_2_65_2
  doi: 10.3987/R-1976-01-0035
– ident: e_1_2_2_58_2
  doi: 10.1002/ange.200602917
– ident: e_1_2_2_8_2
  doi: 10.1021/cr050041j
– ident: e_1_2_2_51_2
  doi: 10.1002/ange.200461598
– ident: e_1_2_2_64_2
– ident: e_1_2_2_37_2
  doi: 10.1016/S0040-4039(03)00686-5
– ident: e_1_2_2_51_3
  doi: 10.1002/anie.200461598
– ident: e_1_2_2_24_2
  doi: 10.1016/S0960-894X(02)00737-0
– ident: e_1_2_2_38_2
  doi: 10.1016/0040-4039(95)00005-W
– ident: e_1_2_2_57_2
  doi: 10.1021/ol0168216
– ident: e_1_2_2_30_2
  doi: 10.1016/j.bmc.2006.06.047
– ident: e_1_2_2_42_2
  doi: 10.1016/j.jorganchem.2010.06.017
– ident: e_1_2_2_22_2
  doi: 10.1016/S0040-4020(00)00448-8
– ident: e_1_2_2_10_2
– ident: e_1_2_2_44_2
  doi: 10.3987/COM-08-S(F)7
– ident: e_1_2_2_47_2
– ident: e_1_2_2_2_2
  doi: 10.1002/ange.200800497
– ident: e_1_2_2_11_2
  doi: 10.1002/ardp.200500194
– ident: e_1_2_2_1_2
– ident: e_1_2_2_33_2
  doi: 10.1021/ja01541a050
– ident: e_1_2_2_14_2
  doi: 10.1016/j.bmcl.2011.01.033
– ident: e_1_2_2_55_2
  doi: 10.1039/c0sc00107d
– ident: e_1_2_2_56_2
  doi: 10.1021/ja016226z
– ident: e_1_2_2_27_2
  doi: 10.1002/cber.188301601154
– ident: e_1_2_2_59_2
  doi: 10.1021/ol062978s
– ident: e_1_2_2_20_2
– ident: e_1_2_2_29_2
– ident: e_1_2_2_52_2
  doi: 10.1021/ol802624e
– ident: e_1_2_2_15_2
– ident: e_1_2_2_49_2
  doi: 10.1016/j.tet.2010.05.046
– ident: e_1_2_2_26_2
– ident: e_1_2_2_4_2
– start-page: 2053
  year: 1966
  ident: WOS:A19668520600011
  article-title: TRIAZAPHENANTHRENES .6. FURTHER OBSERVATIONS ON WIDMAN-STOERMER AND BORSCHE REACTIONS
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC
– volume: 74
  start-page: 3558
  year: 2009
  ident: WOS:000265554900048
  article-title: [4+2] Cycloaddition Reaction of C-Aryl Ketenimines with PTAD as a Synthetic Equivalent of Dinitrogen. Synthesis of Triazolocinnolines and Cinnolines
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo900304a
– volume: 45
  start-page: 7079
  year: 2006
  ident: WOS:000241976300034
  article-title: Domino Cu-catalyzed C-N coupling/hydroamidation: A highly efficient synthesis of nitrogen heterocycles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200602917
– volume: 7
  start-page: 1591
  year: 1999
  ident: WOS:000082137500012
  article-title: Indolo[3,2-c]cinnolines with antiproliferative, antifungal, and antibacterial activity
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
– volume: 16
  start-page: 1850
  year: 2006
  ident: WOS:000236402500017
  article-title: Synthesis and antifungal activity of 6-hydroxycinnolines
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2006.01.005
– volume: 41
  start-page: 1534
  year: 2008
  ident: WOS:000261000000012
  article-title: Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/ar800098p
– volume: 12
  start-page: 795
  year: 2004
  ident: WOS:000188964600015
  article-title: 11H-Isoquino[4,3-c]cinnolin-12-ones: novel anticancer agents with potent topoisomerase I-targeting activity and cytotoxicity
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2003.10.061
– volume: 123
  start-page: 7727
  year: 2001
  ident: WOS:000170299800042
  article-title: A general and efficient copper catalyst for the amidation of aryl halides and the N-arylation of nitrogen heterocycles
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 3
  start-page: 3803
  year: 2001
  ident: WOS:000172181700051
  article-title: Synthesis of N-aryl hydrazides by copper-catalyzed coupling of hydrazides with aryl iodides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol0168216
– volume: 36
  start-page: 1383
  year: 1995
  ident: WOS:A1995QK51800001
  article-title: TRIFLUOROMETHYL GROUP IN THE SYNTHESIS OF HETEROCYCLIC-COMPOUNDS - NEW AND EFFICIENT SYNTHESIS OF 3-ARYL-4-AMINOCINNOLINES
  publication-title: TETRAHEDRON LETTERS
– volume: 16
  start-page: 677
  year: 1883
  ident: 000304814000038.50
  publication-title: Chem. Ber.
– volume: 57
  start-page: 1609
  year: 2001
  ident: WOS:000167054100020
  article-title: Efficient synthesis of 3-aroylcinnolines from aryl methyl ketones
  publication-title: TETRAHEDRON
– volume: 6
  start-page: 2005
  year: 2011
  ident: WOS:000294112200021
  article-title: Bis-Cinnolines as n-Type Semiconducting Material with High Electron Mobility and Thermal Stability and their Application in Organic Photovoltaic Cells
  publication-title: CHEMISTRY-AN ASIAN JOURNAL
  doi: 10.1002/asia.201100234
– volume: 47
  start-page: 6338
  year: 2008
  ident: WOS:000258584800004
  article-title: Biaryl phosphane ligands in palladium-catalyzed amination
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200800497
– volume: 5
  year: 1953
  ident: 000304814000038.42
  publication-title: The Chemistry of Heterocyclic Compounds, Condensed Pyridazine and Pyrazine Rings, Cinnolines, Phthalazines and Quinoxalines
– volume: 77
  start-page: 273
  year: 2009
  ident: WOS:000263374600025
  article-title: NOVEL PROCESS TO 4,4-DIALKYL-1,4-DIHYDRO-6-METHOXY-3-PHENYLCINNOLINES VIA GRIGNARD REACTION
  publication-title: HETEROCYCLES
  doi: 10.3987/COM-08-S(F)7
– volume: 52
  start-page: 2952
  year: 2009
  ident: WOS:000265911800033
  article-title: Heteroaromatic Rings of the Future
  publication-title: JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1021/jm801513z
– volume: 9
  start-page: 641
  year: 2011
  ident: WOS:000286431500001
  article-title: Copper catalysis in the construction of indole and benzo[b]furan rings
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c0ob00501k
– start-page: 392
  year: 1950
  ident: WOS:A1950UB59000086
  article-title: CINNOLINES .26. SOME 4-CINNOLYLHYDRAZINES, THEIR PREPARATION AND OXIDATION - MISCELLANEOUS QUINOLINE DERIVATIVES
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY
– volume: 130
  start-page: 13552
  year: 2008
  ident: WOS:000259924000022
  article-title: A highly active catalyst for Pd-catalyzed amination reactions: Cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja8055358
– volume: 333
  start-page: 341
  year: 2000
  ident: WOS:000165128800005
  article-title: Pyridazine N-oxides. III - Synthesis and "in vitro"' antimicrobial properties of N-oxide derivatives based on tricyclic indeno[2,1-c]pyridazine and benzo[f]cinnoline systems
  publication-title: ARCHIV DER PHARMAZIE
– volume: 104
  start-page: 2127
  year: 2004
  ident: WOS:000221418500002
  article-title: Transition-metal-catalyzed reactions in heterocyclic synthesis
  publication-title: CHEMICAL REVIEWS
– volume: 65
  start-page: 8940
  year: 2009
  ident: WOS:000271345600005
  article-title: Palladium-catalysed tandem alkenyl- and aryl-C-N bond formation: a cascade N-annulation route to 1-functionalised 7-azaindoles
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2009.08.046
– start-page: 1
  year: 2011
  ident: WOS:000286506800004
  article-title: Palladium- and Copper-Catalyzed Aryl Halide Amination, Etherification and Thioetherification Reactions in the Synthesis of Aromatic Heterocycles
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-0030-1258294
– volume: 9
  start-page: 973
  year: 2007
  ident: WOS:000244735900007
  article-title: Copper-catalyzed vinylation of hydrazides. A regioselective entry to highly substituted pyrroles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol062978s
– volume: 340
  start-page: 65
  year: 2007
  ident: WOS:000244909700001
  article-title: Cinnoline derivatives with biological activity
  publication-title: ARCHIV DER PHARMAZIE
– volume: 40
  start-page: 5111
  year: 1999
  ident: WOS:000081250300003
  article-title: A novel synthesis of 3,4-disubstituted cinnolines from o-trifluorophenyl hydrazones
  publication-title: TETRAHEDRON LETTERS
– volume: 14
  start-page: 6832
  year: 2006
  ident: WOS:000241227400005
  article-title: Synthesis and SAR of indazole-pyridine based protein kinase B/Akt inhibitors
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2006.06.047
– volume: 19
  start-page: 2927
  year: 2011
  ident: WOS:000289834600016
  article-title: Development and SAR of functionally selective allosteric modulators of GABA(A) receptors
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
  doi: 10.1016/j.bmc.2011.03.035
– volume: 2
  start-page: 27
  year: 2011
  ident: WOS:000285009500003
  article-title: Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c0sc00331j
– volume: 11
  start-page: 583
  year: 2009
  ident: WOS:000262913500022
  article-title: Cascade Palladium-Catalyzed Alkenyl Aminocarbonylation/Intramolecular Aryl Amidation: An Annulative Synthesis of 2-Quinolones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol802624e
– volume: 120
  start-page: 6438
  year: 2008
  ident: 000304814000038.44
  publication-title: Angew. Chem.
– volume: 20
  start-page: 137
  year: 2010
  ident: WOS:000272935600027
  article-title: Addressing species specific metabolism and solubility issues in a quinoline series of oral PDE4 inhibitors
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2009.11.010
– volume: 44
  start-page: 3493
  year: 2003
  ident: WOS:000182267000013
  article-title: An efficient and facile synthesis of substituted cinnoline and benzo[h]cinnoline derivatives
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/S0040-4039(03)00686-5
– start-page: 2102
  year: 1952
  ident: WOS:A1952UB67400022
  article-title: CINNOLINES .28. THE NATURE OF THE C(3)-POSITION .1. THE BER-BOSSEL SYNTHESIS OF 3-HYDROXYCINNOLINE
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY
– volume: 44
  start-page: 403
  year: 2005
  ident: WOS:000226425600008
  article-title: Palladium-catalyzed tandem alkenyl and aryl C-N bond formation: A cascade N-annulation route to 1-functionalized indoles
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200461598
– volume: 15
  start-page: 3759
  year: 2003
  ident: WOS:000185747100007
  article-title: Synthesis and properties of novel highly fluorescent pyrrolopyridazine derivatives
  publication-title: CHEMISTRY OF MATERIALS
  doi: 10.1021/cm0340532
– volume: 696
  start-page: 37
  year: 2011
  ident: WOS:000285918100005
  article-title: Formation of cinnoline derivatives by a gold(I)-catalyzed hydroarylation of N-propargyl-N '-arylhydrazines
  publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY
  doi: 10.1016/j.jorganchem.2010.06.017
– volume: 56
  start-page: 5499
  year: 2000
  ident: WOS:000088275700025
  article-title: Synthesis of 4,8-diarylcinnolines and quinazolines with potential applications in nonlinear optics. Diazines. part 28
  publication-title: TETRAHEDRON
– volume: 2
  start-page: 3825
  year: 2000
  ident: WOS:000165616300018
  article-title: Thermal cyclization of (2-ethynylphenyl)triazenes: Facile synthesis of substituted cinnolines and isoindazoles
  publication-title: ORGANIC LETTERS
– volume: 41
  start-page: 771
  year: 2000
  ident: WOS:000085038700045
  article-title: An unknown route of cyclocondensation of peri-acetylenylquinones with hydrazine
  publication-title: TETRAHEDRON LETTERS
– volume: 48
  start-page: 7578
  year: 2007
  ident: WOS:000250310800004
  article-title: Copper-catalysed benzofuran synthesis: developing aryl bromide-alkenyl triflates as general heterocycle precursors
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2007.08.109
– volume: 108
  start-page: 3395
  year: 2008
  ident: WOS:000259077600024
  article-title: Coinage metal-assisted synthesis of heterocycles
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr050041j
– volume: 41
  start-page: 1461
  year: 2008
  ident: WOS:000261000000005
  article-title: Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/ar800036s
– volume: 348
  start-page: 851
  year: 2006
  ident: WOS:000237745100011
  article-title: 2-(2-haloalkenyl)-aryl halides as substrates for palladium-catalysed tandem C-N bond formation: Efficient synthesis of 1-substituted indoles
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.200505484
– volume: 21
  start-page: 1382
  year: 2011
  ident: WOS:000287440000019
  article-title: 3-Amido-4-anilinocinnolines as a novel class of CSF-1R inhibitor
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  doi: 10.1016/j.bmcl.2011.01.033
– volume: 118
  start-page: 7237
  year: 2006
  ident: 000304814000038.26
  publication-title: Angew. Chem.
– volume: 4
  start-page: 35
  year: 1976
  ident: WOS:A1976BA45700007
  article-title: CALCULATED REACTIVITY INDEXES AND BOND DISTANCES FOR THIENO[2,3-C]PYRIDAZINE
  publication-title: HETEROCYCLES
– volume: 12
  start-page: 3333
  year: 2002
  ident: WOS:000178916300022
  article-title: Diaza- and triazachrysenes: Potent topoisomerase-targeting agents with exceptional antitumor activity against the human tumor xenograft, MDA-MB-435
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
– volume: 9
  start-page: 6873
  year: 2011
  ident: WOS:000295889900001
  article-title: Tandem reactions initiated by copper-catalyzed cross-coupling: A new strategy towards heterocycle synthesis
  publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY
  doi: 10.1039/c1ob05769c
– volume: 80
  start-page: 1981
  year: 1958
  ident: WOS:A1958WB38300050
  article-title: CINNOLINES .4. SYNTHESIS OF 3-ACETYL-CARBETHOXYCINNOLINES AND 3-CARBETHOXYCINNOLINES
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 66
  start-page: 6632
  year: 2010
  ident: WOS:000280902200040
  article-title: Palladium catalyzed tandem alkenyl- and aryl-C-N bond formation: a cascade N-annulation route to 4-, 5-, 6-and 7-chloroindoles
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2010.05.046
– volume: 37
  start-page: 3513
  year: 1981
  ident: WOS:A1981MM18400011
  article-title: FUNCTIONALIZED ENAMINES .30. REACTION OF BETA-AMINO-ALPHA,BETA-UNSATURATED ESTERS AND AMIDES WITH ARYL DIAZONIUM SALTS - SYNTHESIS OF CINNOLINE DERIVATIVES
  publication-title: TETRAHEDRON
– volume: 11
  start-page: 1475
  year: 2003
  ident: WOS:000181715100032
  article-title: Substituted dibenzo[c,h]cinnolines: Topoisomerase I-targeting anticancer agents
  publication-title: BIOORGANIC & MEDICINAL CHEMISTRY
– volume: 1
  start-page: 13
  year: 2010
  ident: WOS:000281247900002
  article-title: Diamine ligands in copper-catalyzed reactions
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c0sc00107d
– volume: 117
  start-page: 407
  year: 2005
  ident: 000304814000038.52
  publication-title: Angew. Chem.
SSID ssj0028806
Score 2.3404217
Snippet Cinn‐tillating synthesis: The combination of a readily available copper catalyst, a simple hydrazide nucleophile, and established difunctionalized building...
Cinn-tillating synthesis: The combination of a readily available copper catalyst, a simple hydrazide nucleophile, and established difunctionalized building...
Source Web of Science
SourceID proquest
pubmed
webofscience
crossref
wiley
istex
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 5718
SubjectTerms annulation
Bonding
Carbon - chemistry
Catalysis
Catalysts
Chemistry
Chemistry, Multidisciplinary
cinnolines
Copper
Copper - chemistry
copper catalysis
Cyclization
heterocycles
Heterocyclic Compounds, 2-Ring - chemical synthesis
Heterocyclic Compounds, 2-Ring - chemistry
Hydrazides
Hydrazines - chemistry
Nitrogen - chemistry
Nucleophiles
Physical Sciences
Science & Technology
Synthesis
tandem processes
Title Copper-Catalyzed Tandem CN Bond Formation: An Efficient Annulative Synthesis of Functionalized Cinnolines
URI https://api.istex.fr/ark:/67375/WNG-CQ96WZKK-N/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201201529
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000304814000038
https://www.ncbi.nlm.nih.gov/pubmed/22539417
https://www.proquest.com/docview/1017986776
https://www.proquest.com/docview/1701123781
Volume 51
WOS 000304814000038
WOSCitedRecordID wos000304814000038
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3bbtQwEB2h8gAv3C_hJiNV8JR2EztOzNsq2qVQEQlo1YoXy44dadWSXe1Fon3iE_iHfkj_pT_QX8DjbEK34iaQ8pAok0QZjz3H9swZgPVSiMQYpcLIJlXoPFQZausaJBLGRkaLypaYKPyu4Fu77O1-sn8hi7_hh-gW3LBn-PEaO7jSs80fpKGYgY2hWe5IYszgw4AtREUfOv6o2Blnk15EaYhV6FvWxl68ufr4ile6igr-8jPIeck7rQJa75GGN0G1_9IEohxsLOZ6ozy-RPP4Pz97C24s4SrpN_Z1G67Y-g5cy9sqcXehzseTiZ2eff2W40LQ0bE1ZAcXpj-T_PzktCBYt5gM2xTJV6Rfk4GnrXDejiC7_6GnHicfj2qHRWejGRlXZOi8bbNIOcIX5iOsiY0B-vdgdzjYybfCZQ2HsHRQT4Q24c5IME_TaoaTs4Q7SFLFieWm5DifUlopLlIT9UxsrFYstZnhgvWMppTR-7BWj2v7EEiVUV0JB6l0mSIpfiY0zUzFE8FKqhkLIGzbUJZLgnOss3EoG2rmWKIWZafFAF528pOG2uOXki-8SXRianqAAXFpIveK1zJ_L_jep-1tWQTwvLUZ6doB915UbceLmfQjH3IH8t_IpG6wjWmaRQE8aAyu-6IbdqlgURrA-kUL7O77uS1D-jK_2RtA9Ddi-VJNyH8wDyD2JvgHZch-8WbQXT36l4cew3U89xF37AmszacL-9Rhu7l-5vvvd9rYRlg
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NbtQwEB5BeygXyj8pf0aq4JR2EzvOmtsq7LJl20jAVkW9WHHsSKuW7Gp_JNoTj8A78CC8Cy_AK-BxNoGt-BNIuSQZJ_J47BmPZ74B2M6FiLTOMj8wUeFbDZX7ytgBCYQ2gVaiMDkmCh-kvH_IXr6N6mhCzIWp8CEahxvODLde4wRHh_Tud9RQTMHG2Cx7RaG4DOtY1hvh85-_bhCkQiueVYIRpT7Woa9xG1vh7mr7Fb20jix-_zOj84J-WjVpnU7qbYKqe1OFopzsLOZqJz-_APT4X929BleXFivpVCJ2HS6Z8gZsJHWhuJtQJuPJxEy_fPiYoC_o7NxoMkTf9DuSfP30OSVYupj06izJZ6RTkq5DrrAKjyDA_6lDHydvzkprjs5GMzIuSM8q3MpPOcIPJiMsi40x-rfgsNcdJn1_WcbBz621J3wTcSsnmKppFMP9WcStVVKEkeE657ilylSWcRHroKVDbVTGYtPWXLCWVpQyehvWynFp7gIp2lQVwlpVKo8RF78tFG3rgkeC5VQx5oFfD6LMlxjnWGrjVFbozKFELsqGix48begnFbrHLymfOJloyLLpCcbExZE8Sl_I5JXgR8eDgUw9eFwLjbTjgMcvWWnGi5l0ix_CB_Lf0MR2vQ1p3A48uFNJXPNHu_JSwYLYg-0fRbB577a3DBHM3HmvB8HfkCVLNiEEwtyD0MngH5ghO-let7nb-pdGj2CjPzzYl_t76eAeXMHnLgCP3Ye1-XRhHlhTb64eusn8DSXOSnQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3bbtQwEB1BKwEv3C_haqQKntJuYseJeVulu7QsRFxateqLFceOtGrJrvYi0T7xCfwDH8K_8AP8Ah5nE7oVN4GUlyTjRB6PPePxzBmAtUKISOs89wMTlb7VUIWvjB2QQGgTaCVKU2Ci8KuMb-2yF_vR_qks_hofonW44cxw6zVO8LEuN36AhmIGNoZm2SsKxXlYZbwjsHjD5tsWQCq00lnnF1HqYxn6BraxE24st19SS6vI4Q8_sznPqKdli9appP4VyJvO1JEoh-vzmVovTs7gPP5Pb6_C5YW9Srq1gF2Dc6a6DhfTpkzcDajS0XhsJl8_fkrRE3R8YjTZQc_0e5J--_wlI1i4mPSbHMlnpFuRnsOtsOqOILz_kcMeJ--OK2uMTodTMipJ36rb2ks5xA-mQyyKjRH6N2G339tJt_xFEQe_sLae8E3ErZRgoqZRDHdnEbc2SRlGhuuC44YqV3nORayDjg61UTmLTaK5YB2tKGX0FqxUo8rcAVImVJXC2lSqiBEVPxGKJrrkkWAFVYx54DdjKIsFwjkW2jiSNTZzKJGLsuWiB09b-nGN7fFLyidOJFqyfHKIEXFxJPey5zJ9I_jewWAgMw8eNzIj7Tjg4UtemdF8Kt3Sh-CB_Dc0sV1tQxongQe3a4Fr_2jXXSpYEHuwdloC2_duc8sQv8yd9noQ_A1ZumATAiDMPAidCP6BGbKbbffau7v_0ugRXHi92Zcvt7PBPbiEj130HbsPK7PJ3Dywdt5MPXRT-TsELkkj
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=Copper%E2%80%90Catalyzed+Tandem+C%EF%A3%BFN+Bond+Formation%3A+An+Efficient+Annulative+Synthesis+of+Functionalized+Cinnolines&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Ball%2C+Catherine+J.&rft.au=Gilmore%2C+Jeremy&rft.au=Willis%2C+Michael+C.&rft.date=2012-06-04&rft.issn=1433-7851&rft.eissn=1521-3773&rft.volume=51&rft.issue=23&rft.spage=5718&rft.epage=5722&rft_id=info:doi/10.1002%2Fanie.201201529&rft.externalDBID=n%2Fa&rft.externalDocID=10_1002_anie_201201529
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon