Palladium-Catalyzed Annulation of Acyloximes with Arynes (or Alkynes): Synthesis of Phenanthridines and Isoquinolines

Intermolecular insertion: A palladium‐catalyzed domino aminopalladation/ CH functionalization sequence has been developed, and provides access to functionalized phenanthridines and isoquinolines (see scheme; Tf=triflate, TMS=trimethylsilyl, M.S.=molecular sieves). The use of butyronitrile as the so...

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Published inAngewandte Chemie (International ed.) Vol. 48; no. 3; pp. 572 - 577
Main Authors Gerfaud, Thibaud, Neuville, Luc, Zhu, Jieping
Format Journal Article
LanguageEnglish
Published Weinheim Wiley-VCH Verlag 01.01.2009
WILEY‐VCH Verlag
Wiley
Subjects
arynes
Cellular Biology
Chemistry
Chemistry, Multidisciplinary
domino reactions
heterocycles
Life Sciences
oximes
palladium
Physical Sciences
Science & Technology
ORGANIC-SYNTHESIS
O BOND-CLEAVAGE
oximes
arynes
domino reactions
heterocycles
AMINO-HECK
HIGHLY EFFICIENT ROUTE
ARYL HALIDES
PYRROLE DERIVATIVES
palladium
2+2+2 COCYCLIZATION
N-ARYLATION
OXIDATIVE AMINATION
CYCLIZATION
Online AccessGet full text
ISSN1433-7851
1521-3773
1521-3773
DOI10.1002/anie.200804683

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Abstract Intermolecular insertion: A palladium‐catalyzed domino aminopalladation/ CH functionalization sequence has been developed, and provides access to functionalized phenanthridines and isoquinolines (see scheme; Tf=triflate, TMS=trimethylsilyl, M.S.=molecular sieves). The use of butyronitrile as the solvent is determinant to the success of the domino process.
AbstractList Intermolecular insertion: A palladium‐catalyzed domino aminopalladation/ CH functionalization sequence has been developed, and provides access to functionalized phenanthridines and isoquinolines (see scheme; Tf=triflate, TMS=trimethylsilyl, M.S.=molecular sieves). The use of butyronitrile as the solvent is determinant to the success of the domino process.
Author Gerfaud, Thibaud
Neuville, Luc
Zhu, Jieping
Author_xml – sequence: 1
  fullname: Gerfaud, Thibaud
– sequence: 2
  fullname: Neuville, Luc
– sequence: 3
  fullname: Zhu, Jieping
BackLink https://www.ncbi.nlm.nih.gov/pubmed/19067452$$D View this record in MEDLINE/PubMed
https://hal.science/hal-00369901$$DView record in HAL
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Cites_doi 10.1039/b602664h
10.1002/ejoc.200500389
10.1021/ol7029799
10.1039/B411438H
10.1021/ja055781o
10.1002/chem.200601016
10.1021/ja8013743
10.1002/ange.200462215
10.1016/S0040-4020(02)01563-6
10.1021/ja973524g
10.1039/a707213i
10.1021/ol047628p
10.1002/anie.200462215
10.1002/tcr.10030
10.1002/0471212466.ch42
10.1021/jo070625g
10.1021/ja001205a
10.1246/bcsj.75.1451
10.1016/S0010-8545(98)00215-X
10.1080/00304940809458089
10.1246/cl.1983.1211
10.1055/s-2005-869966
10.1246/bcsj.76.1055
10.1071/CH07132
10.1055/s-2001-14637
10.1021/jo000535a
10.1246/cl.1999.45
10.1021/ja9907111
10.1002/(SICI)1521-3749(199804)624:4<737::AID-ZAAC737>3.0.CO;2-L
10.1021/ja005558l
10.1002/ange.200604969
10.1021/jo049385k
10.1002/anie.200460189
10.1021/ja058418q
10.1016/S0040-4039(99)01526-9
10.3762/bjoc.4.10
10.1021/ol048891t
10.1021/ja0362149
10.1021/ol036091x
10.1002/ange.200460189
10.1246/bcsj.77.785
10.1021/om00042a040
10.1002/ange.200605192
10.1021/cr040639b
10.1021/ja011923c
10.1021/jo800266y
10.1039/p19760002285
10.1002/anie.200400655
10.1021/cr0509760
10.1002/anie.200604969
10.1002/anie.200605192
10.1021/ja056165v
10.1002/anie.200351923
10.1021/cr030681r
10.1021/ja047472o
10.1021/ic061997v
10.1016/j.tet.2006.10.071
10.1002/ange.200351923
10.1002/anie.200390151
10.1021/ol061258i
10.1021/cr990281x
10.1002/(SICI)1521-3757(20000103)112:1<185::AID-ANGE185>3.0.CO;2-N
10.1039/b515481m
10.1002/ange.200400655
10.1021/ol050859r
10.1002/anie.200352808
10.1021/jo991342u
10.1002/(SICI)1521-3773(19981016)37:19<2659::AID-ANIE2659>3.0.CO;2-4
10.1002/adsc.200600587
10.1021/ja0264091
10.1246/cl.2001.526
10.1021/ja0615526
10.1021/jo800847h
10.1002/(SICI)1521-3757(19981002)110:19<2804::AID-ANGE2804>3.0.CO;2-2
10.1021/ja0680562
10.1039/b801870g
10.1021/ja027683y
10.1021/ja051181d
10.1002/ange.200453809
10.1055/s-2006-951516
10.1002/(SICI)1521-3773(20000103)39:1<173::AID-ANIE173>3.0.CO;2-F
10.1021/ol702584t
10.1002/ange.200390119
10.1021/ol800080w
10.1002/anie.200453809
10.1002/adsc.200505158
10.1021/ol0611954
10.1039/B607474J
10.1021/ol062022h
10.1021/jo010162t
10.1021/ol061755z
10.1016/S0040-4039(97)01465-2
10.1002/ange.200352808
10.1246/cl.2002.606
10.1021/ol070900l
10.1021/jo01348a046
10.1016/S0040-4039(00)61007-9
10.1055/s-2008-1072728
10.1002/anie.200500390
10.1016/j.jfluchem.2005.12.023
10.1002/0471264180.OR035.01
10.1039/b411438h
10.1039/b607474j
10.1039/B515481M
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Issue 3
Keywords ORGANIC-SYNTHESIS
O BOND-CLEAVAGE
oximes
arynes
domino reactions
heterocycles
AMINO-HECK
HIGHLY EFFICIENT ROUTE
ARYL HALIDES
PYRROLE DERIVATIVES
palladium
2+2+2 COCYCLIZATION
N-ARYLATION
OXIDATIVE AMINATION
CYCLIZATION
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0
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Notes http://dx.doi.org/10.1002/anie.200804683
Financial support from CNRS and the Institut de Chimie des Substances Naturelles are gratefully acknowledged. T.G. thanks the institute for a doctoral fellowships.
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PublicationTitle Angewandte Chemie (International ed.)
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References 2007; 349
2004; 126
2004; 69
1976
1999; 121
2003; 59
2004; 6
1988; 35
2007; 72
1999; 40
2007 2005; 107
2008; 4
2008; 73
1992; 11
2007; 36
2004; 77
2001
2005; 105
1999; 181
2007; 9
2003; 5
2007; 60
1983
2000; 122
2007; 63
2003; 125
2006; 128
2005; 34
1998; 120
2005 2005; 117 44
2004 2004; 116 43
2001; 123
2007; 129
2002; 75
2000; 65
1998
2002; 2
2008
2006; 8
2006
2005
2008; 10
2002
2001; 66
1992; 33
2007; 13
2003; 76
1966; 31
1999
2003 2003; 115 42
2002; 124
2005; 127
1998; 624
2005; 7
1997; 38
2000; 100
1998 1998; 110 37
2007 2007; 119 46
2008; 40
2000 2000; 112 39
2006; 348
2008; 130
2007; 46
e_1_2_3_50_2
e_1_2_3_92_2
e_1_2_3_114_2
e_1_2_3_114_3
e_1_2_3_110_2
e_1_2_3_4_2
e_1_2_3_16_2
e_1_2_3_39_2
e_1_2_3_8_2
e_1_2_3_12_2
e_1_2_3_58_2
e_1_2_3_12_3
e_1_2_3_77_2
e_1_2_3_35_2
Guitiàn E. (e_1_2_3_64_2) 2005
(e_1_2_3_56_3) 2005
e_1_2_3_54_2
e_1_2_3_73_2
e_1_2_3_96_2
e_1_2_3_31_2
e_1_2_3_81_2
e_1_2_3_102_2
e_1_2_3_28_2
e_1_2_3_47_2
e_1_2_3_66_2
e_1_2_3_89_2
e_1_2_3_106_2
e_1_2_3_20_2
e_1_2_3_43_2
e_1_2_3_62_2
Muci A. R. (e_1_2_3_3_2) 2002
e_1_2_3_72_2
e_1_2_3_91_2
e_1_2_3_15_2
e_1_2_3_38_2
e_1_2_3_111_2
e_1_2_3_38_3
e_1_2_3_11_2
e_1_2_3_34_2
e_1_2_3_7_2
e_1_2_3_76_3
e_1_2_3_57_2
e_1_2_3_99_2
e_1_2_3_30_2
e_1_2_3_76_2
e_1_2_3_53_2
e_1_2_3_95_2
Zhu J.‐L. (e_1_2_3_21_2) 2008
e_1_2_3_61_2
e_1_2_3_80_2
e_1_2_3_103_2
e_1_2_3_27_2
e_1_2_3_23_2
e_1_2_3_69_2
e_1_2_3_46_2
e_1_2_3_88_2
Ichikawa J. (e_1_2_3_19_2) 2006
e_1_2_3_65_2
e_1_2_3_42_2
e_1_2_3_84_2
e_1_2_3_107_2
e_1_2_3_71_2
e_1_2_3_94_2
e_1_2_3_71_3
e_1_2_3_90_2
e_1_2_3_112_2
e_1_2_3_37_2
e_1_2_3_2_2
e_1_2_3_18_2
e_1_2_3_56_2
e_1_2_3_79_2
e_1_2_3_33_2
e_1_2_3_6_2
e_1_2_3_14_2
e_1_2_3_52_2
e_1_2_3_75_2
e_1_2_3_98_2
e_1_2_3_10_2
e_1_2_3_60_2
e_1_2_3_83_2
e_1_2_3_104_2
e_1_2_3_26_2
e_1_2_3_49_2
e_1_2_3_100_2
e_1_2_3_22_2
e_1_2_3_45_2
e_1_2_3_68_2
e_1_2_3_68_3
e_1_2_3_108_3
e_1_2_3_41_2
e_1_2_3_87_2
Gawly R. E. (e_1_2_3_85_2) 1988; 35
e_1_2_3_108_2
e_1_2_3_41_3
Kitamura M. (e_1_2_3_24_2) 2006
e_1_2_3_93_2
e_1_2_3_70_2
e_1_2_3_1_2
e_1_2_3_113_2
e_1_2_3_5_2
e_1_2_3_17_2
e_1_2_3_59_2
e_1_2_3_59_3
e_1_2_3_9_2
e_1_2_3_32_3
e_1_2_3_55_2
e_1_2_3_13_2
e_1_2_3_36_2
e_1_2_3_78_2
e_1_2_3_51_2
e_1_2_3_97_2
e_1_2_3_32_2
e_1_2_3_74_2
e_1_2_3_82_2
e_1_2_3_101_2
e_1_2_3_48_2
e_1_2_3_29_2
e_1_2_3_44_2
e_1_2_3_109_2
e_1_2_3_25_2
e_1_2_3_67_2
e_1_2_3_63_3
e_1_2_3_40_2
e_1_2_3_86_2
e_1_2_3_105_2
e_1_2_3_63_2
Bonnaterre, F (WOS:000256826500001) 2008; 4
Tsutsui, H (WOS:000078361400023) 1999
Thomas, PJ (WOS:000247599400015) 2007; 9
Liu, S (WOS:000256301200013) 2008; 130
Kappe, CO (WOS:000225575600006) 2004; 43
Dupont, J (WOS:000229729000017) 2005; 105
MASON, MR (WOS:A1992HY67400040) 1992; 11
Wenk, HH (WOS:000181379500003) 2003; 42
Pinto, A (WOS:000246282900020) 2007; 46
YOSHIKAWA E (WOS:000262539800023.97) 2000; 112
Peña, D (WOS:000081152200037) 1999; 121
Bonnaterre, F (WOS:000240339700045) 2006; 8
Chiba, S (WOS:000221089300024) 2004; 77
Tang, S (WOS:000254032100036) 2008; 10
Saito, S (WOS:000088838500007) 2000; 100
Timokhin, VI (WOS:000186123900005) 2003; 125
Liu, ZJ (WOS:000243662300008) 2007; 63
Sanz, R (WOS:000256822100001) 2008; 40
Jeganmohan, M (WOS:000223013300046) 2004; 6
Guitián, E (CCC:000232634400005) 2005; 14
Buchwald, SL (WOS:000234964700001) 2006; 348
Peña, D (WOS:000165199000019) 2000; 65
Quintana, I (WOS:000239001500048) 2006; 8
HARTWIG JF (WOS:000262539800023.31) 2002; 1
Nishimura, T (WOS:000223008100024) 2004; 69
HIMESHIMA, Y (WOS:A1983RB99500022) 1983
Wolfe, JP (WOS:A1997XU80200016) 1997; 38
Cuny, G (WOS:000186128300010) 2003; 42
Du, HF (WOS:000243683800019) 2007; 129
de la Hoz, A (WOS:000226522500006) 2005; 34
Jayanth, TT (WOS:000235562900039) 2006; 128
GAWLEY RE (WOS:000262539800023.29) 1988; 35
Peña, D (WOS:000076575900011) 1998; 37
Pinto, A (WOS:000241030900065) 2006; 8
Zhu, JL (WOS:000256803100033) 2008
Salcedo, A (WOS:000255339600044) 2008; 73
Kitamura, M (WOS:000237240500013) 2006
KAPPE CO (WOS:000262539800023.42) 2004; 116
Yoshikawa, E (WOS:000084700400019) 2000; 39
Narasaka, K (WOS:000233144000002) 2005; 2005
Cacchi, S (WOS:000230522900006) 2005; 105
Rayabarapu, DK (WOS:000168907700063) 2001; 66
García-Cuadrado, D (WOS:000234941100017) 2006; 128
Mann, G (WOS:000071889300030) 1998; 120
Kitamura, M (WOS:000176347400026) 2002
Tsutsui, H (WOS:000169538700024) 2001
Enquist, PA (WOS:000187038300031) 2003; 5
LIU Z (WOS:000262539800023.53) 2007; 119
Xie, CS (WOS:000247612200058) 2007; 72
Kitamura, M (WOS:000169286700022) 2001
Zaman, S (WOS:000248651300012) 2007; 60
Chatani, N (WOS:000172745300032) 2001; 123
CUNY G (WOS:000262539800023.16) 2003; 115
Liu, ZJ (WOS:000233535400028) 2005; 127
Pinto, A (WOS:000243622500026) 2007; 13
Portela-Cubillo, F (WOS:000257543100044) 2008; 73
Kitamura, M (WOS:000182372900006) 2002; 2
Ferreira, CMP (WOS:000072111100003) 1998
Muci, AR (WOS:000174161500006) 2002; 219
Tillack, A (WOS:000073029100033) 1998; 624
Shimada, T (WOS:000178792400018) 2002; 124
Salcedo, A (WOS:000253519600044) 2008; 10
FIELDS, EK (WOS:A19668354300046) 1966; 31
Zaman, S (WOS:000183391700024) 2003; 76
Kukushkin, VY (WOS:000078163000005) 1999; 181
Yoshida, H (WOS:000224283900018) 2004; 43
Yoshikawa, E (WOS:000088658400015) 2000; 122
Zaman, S (WOS:000226950100022) 2005; 7
Cuny, G (WOS:000224964500049) 2004; 126
Jayanth, TT (WOS:000230213100030) 2005; 7
Hsieh, JC (WOS:000257236600005) 2008
Barluenga, J (WOS:000188213300016) 2004; 43
Campeau, LC (WOS:000236004300001) 2006
WENK HH (WOS:000262539800023.93) 2003; 115
SATO Y (WOS:000262539800023.81) 2004; 116
Henderson, JL (WOS:000251614900065) 2007; 9
Minatti, A (WOS:000247341300011) 2007; 36
Henderson, JL (WOS:000238099500014) 2006; 128
PINTO A (WOS:000262539800023.68) 2007; 119
Bolm, C (WOS:000084816300026) 2000; 65
Retboll, M (WOS:000176843200030) 2002; 124
Nishimura, T (WOS:000165696900058) 2000; 122
Alonso, R (WOS:000239309900028) 2006; 8
Denmark, SE (WOS:000243619600008) 2006
Radhakrishnan, KV (WOS:000082964100023) 1999; 40
Alberico, D (WOS:000243381000008) 2007; 107
Tsutsui, H (WOS:000177224900004) 2002; 75
Sato, Y (WOS:000245379400024) 2007; 349
Fürstner, A (WOS:000229549100022) 2005; 44
BARLUENGA J (WOS:000262539800023.4) 2004; 116
Dyker, G (WOS:000299053100001) 2005
HOSOKAWA, T (WOS:A1992JV80200024) 1992; 33
DENNIS, N (WOS:A1976CM84600014) 1976
Pellissier, H (WOS:000180777200001) 2003; 59
PENA D (WOS:000262539800023.63) 1998; 110
Jeganmohan, M (WOS:000230380900024) 2005
Ichikawa, J (WOS:000237986300005) 2006; 127
Jeganmohan, M (WOS:000238101100007) 2006
Bar, GLJ (WOS:000229244600023) 2005; 127
Kotov, V (WOS:000244798800006) 2007; 46
Sato, Y (WOS:000221307200024) 2004; 43
Liu, ZJ (WOS:000245371300040) 2007; 46
References_xml – volume: 75
  start-page: 1451
  year: 2002
  end-page: 1460
  publication-title: Bull. Chem. Soc. Jpn.
– volume: 100
  start-page: 2901
  year: 2000
  end-page: 2916
  publication-title: Chem. Rev.
– volume: 10
  start-page: 1179
  year: 2008
  end-page: 1182
  publication-title: Org. Lett.
– volume: 349
  start-page: 647
  year: 2007
  end-page: 661
  publication-title: Adv. Synth. Catal.
– volume: 31
  start-page: 3307
  year: 1966
  end-page: 3309
  publication-title: J. Org. Chem.
– volume: 119 46
  start-page: 2587 2535
  year: 2007 2007
  end-page: 2590 2538
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 105
  start-page: 2527
  year: 2005
  end-page: 2572
  publication-title: Chem. Rev.
– volume: 36
  start-page: 1142
  year: 2007
  end-page: 1152
  publication-title: Chem. Soc. Rev.
– start-page: 974
  year: 2001
  end-page: 976
  publication-title: Synlett
– volume: 7
  start-page: 2921
  year: 2005
  end-page: 2924
  publication-title: Org. Lett.
– volume: 110 37
  start-page: 2804 2659
  year: 1998 1998
  end-page: 2806 2661
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 123
  start-page: 12686
  year: 2001
  end-page: 12687
  publication-title: J. Am. Chem. Soc.
– volume: 9
  start-page: 2665
  year: 2007
  end-page: 2668
  publication-title: Org. Lett.
– volume: 9
  start-page: 5589
  year: 2007
  end-page: 5592
  publication-title: Org. Lett.
– volume: 124
  start-page: 12670
  year: 2002
  end-page: 12671
  publication-title: J. Am. Chem. Soc.
– volume: 126
  start-page: 14475
  year: 2004
  end-page: 14484
  publication-title: J. Am. Chem. Soc.
– volume: 2
  start-page: 268
  year: 2002
  end-page: 277
  publication-title: Chem. Rec.
– volume: 129
  start-page: 762
  year: 2007
  end-page: 763
  publication-title: J. Am. Chem. Soc.
– volume: 8
  start-page: 3521
  year: 2006
  end-page: 3523
  publication-title: Org. Lett.
– start-page: 1693
  year: 2005
  end-page: 1697
  publication-title: Synthesis
– volume: 34
  start-page: 164
  year: 2005
  end-page: 178
  publication-title: Chem. Soc. Rev.
– volume: 107
  start-page: 174
  year: 2007 2005
  end-page: 238
  publication-title: Chem. Rev.
– volume: 11
  start-page: 2212
  year: 1992
  end-page: 2220
  publication-title: Organometallics
– volume: 119 46
  start-page: 3355 3291
  year: 2007 2007
  end-page: 3359 3295
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 121
  start-page: 5827
  year: 1999
  end-page: 5828
  publication-title: J. Am. Chem. Soc.
– volume: 65
  start-page: 6944
  year: 2000
  end-page: 6950
  publication-title: J. Org. Chem.
– volume: 10
  start-page: 857
  year: 2008
  end-page: 860
  publication-title: Org. Lett.
– volume: 116 43
  start-page: 6408 6250
  year: 2004 2004
  end-page: 6443 6284
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– start-page: 45
  year: 1999
  end-page: 56
  publication-title: Chem. Lett.
– volume: 181
  start-page: 147
  year: 1999
  end-page: 175
  publication-title: Coord. Chem. Rev.
– volume: 624
  start-page: 737
  year: 1998
  end-page: 740
  publication-title: Z. Anorg. Allg. Chem.
– volume: 60
  start-page: 624
  year: 2007
  end-page: 626
  publication-title: Aust. J. Chem.
– start-page: 127
  year: 2006
  end-page: 504
  publication-title: J. Fluorine Chem.
– start-page: 1253
  year: 2006
  end-page: 1264
  publication-title: Chem. Commun.
– volume: 116 43
  start-page: 5162 5052
  year: 2004 2004
  end-page: 5165 5055
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 117 44
  start-page: 2837 2777
  year: 2005 2005
  end-page: 2841 2781
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– start-page: 2285
  year: 1976
  end-page: 2288
  publication-title: J. Chem. Soc. Perkin Trans. 1
– start-page: 133
  year: 2002
  end-page: 205
– volume: 8
  start-page: 3347
  year: 2006
  end-page: 3349
  publication-title: Org. Lett.
– volume: 72
  start-page: 5431
  year: 2007
  end-page: 5434
  publication-title: J. Org. Chem.
– volume: 7
  start-page: 609
  year: 2005
  end-page: 611
  publication-title: Org. Lett.
– volume: 105
  start-page: 2873
  year: 2005
  end-page: 2920
  publication-title: Chem. Rev.
– start-page: 1250
  year: 2008
  end-page: 1254
  publication-title: Synlett
– volume: 35
  start-page: 1
  year: 1988
  end-page: 420
  publication-title: Org. React.
– volume: 5
  start-page: 4875
  year: 2003
  end-page: 4878
  publication-title: Org. Lett.
– start-page: 4505
  year: 2005
  end-page: 4519
  publication-title: Eur. J. Org. Chem.
– volume: 77
  start-page: 785
  year: 2004
  end-page: 796
  publication-title: Bull. Chem. Soc. Jpn.
– volume: 124
  start-page: 8348
  year: 2002
  end-page: 8360
  publication-title: J. Am. Chem. Soc.
– volume: 348
  start-page: 23
  year: 2006
  end-page: 39
  publication-title: Adv. Synth. Catal.
– volume: 13
  start-page: 961
  year: 2007
  end-page: 967
  publication-title: Chem. Eur. J.
– volume: 46
  start-page: 1910
  year: 2007
  end-page: 1923
  publication-title: Inorg. Chem.
– start-page: 2992
  year: 2008
  end-page: 2994
  publication-title: Chem. Commun.
– volume: 128
  start-page: 1066
  year: 2006
  end-page: 1067
  publication-title: J. Am. Chem. Soc.
– volume: 33
  start-page: 6643
  year: 1992
  end-page: 6646
  publication-title: Tetrahedron Lett.
– volume: 76
  start-page: 1055
  year: 2003
  end-page: 1062
  publication-title: Bull. Chem. Soc. Jpn.
– volume: 8
  start-page: 4927
  year: 2006
  end-page: 4930
  publication-title: Org. Lett.
– start-page: 325
  year: 1998
  end-page: 326
  publication-title: J. Chem. Soc. Dalton Trans.
– volume: 73
  start-page: 3600
  year: 2008
  end-page: 3603
  publication-title: J. Org. Chem.
– volume: 116 43
  start-page: 347 343
  year: 2004 2004
  end-page: 349 345
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 128
  start-page: 2232
  year: 2006
  end-page: 2233
  publication-title: J. Am. Chem. Soc.
– start-page: 606
  year: 2002
  end-page: 607
  publication-title: Chem. Lett.
– volume: 8
  start-page: 4351
  year: 2006
  end-page: 4354
  publication-title: Org. Lett.
– volume: 63
  start-page: 347
  year: 2007
  end-page: 355
  publication-title: Tetrahedron
– volume: 4
  start-page: 1
  year: 2008
  end-page: 6
  publication-title: Beilstein J. Org. Chem.
– volume: 69
  start-page: 5342
  year: 2004
  end-page: 5347
  publication-title: J. Org. Chem.
– volume: 127
  start-page: 7308
  year: 2005
  end-page: 7309
  publication-title: J. Am. Chem. Soc.
– volume: 73
  start-page: 5558
  year: 2008
  end-page: 5565
  publication-title: J. Org. Chem.
– volume: 65
  start-page: 169
  year: 2000
  end-page: 175
  publication-title: J. Org. Chem.
– volume: 122
  start-page: 12049
  year: 2000
  end-page: 12050
  publication-title: J. Am. Chem. Soc.
– start-page: 148
  year: 2006
  end-page: 162
  publication-title: ARKIVOC
– start-page: 1211
  year: 1983
  end-page: 1214
  publication-title: Chem. Lett.
– start-page: 109
  year: 2005
  end-page: 146
– volume: 122
  start-page: 7280
  year: 2000
  end-page: 7286
  publication-title: J. Am. Chem. Soc.
– start-page: 1051
  year: 2002
  end-page: 1096
– volume: 66
  start-page: 3646
  year: 2001
  end-page: 3649
  publication-title: J. Org. Chem.
– volume: 40
  start-page: 7533
  year: 1999
  end-page: 7535
  publication-title: Tetrahedron Lett.
– volume: 115 42
  start-page: 518 502
  year: 2003 2003
  end-page: 546 528
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 128
  start-page: 7426
  year: 2006
  end-page: 7427
  publication-title: J. Am. Chem. Soc.
– volume: 40
  start-page: 215
  year: 2008
  end-page: 291
  publication-title: Org. Prep. Proced. Int.
– volume: 115 42
  start-page: 4922 4774
  year: 2003 2003
  end-page: 4925 4777
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– start-page: 2454
  year: 2006
  end-page: 2456
  publication-title: Chem. Commun.
– start-page: 526
  year: 2001
  end-page: 527
  publication-title: Chem. Lett.
– volume: 6
  start-page: 2821
  year: 2004
  end-page: 2824
  publication-title: Org. Lett.
– volume: 130
  start-page: 6918
  year: 2008
  end-page: 6919
  publication-title: J. Am. Chem. Soc.
– volume: 125
  start-page: 12996
  year: 2003
  end-page: 12997
  publication-title: J. Am. Chem. Soc.
– volume: 59
  start-page: 701
  year: 2003
  end-page: 730
  publication-title: Tetrahedron
– start-page: 2921
  year: 2006
  end-page: 2928
  publication-title: Synlett
– volume: 127
  start-page: 15716
  year: 2005
  end-page: 15717
  publication-title: J. Am. Chem. Soc.
– volume: 116 43
  start-page: 2490 2436
  year: 2004 2004
  end-page: 2494 2440
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– volume: 38
  start-page: 6367
  year: 1997
  end-page: 6370
  publication-title: Tetrahedron Lett.
– volume: 120
  start-page: 827
  year: 1998
  end-page: 828
  publication-title: J. Am. Chem. Soc.
– volume: 112 39
  start-page: 185 173
  year: 2000 2000
  end-page: 187 175
  publication-title: Angew. Chem. Angew. Chem. Int. Ed.
– ident: e_1_2_3_90_2
  doi: 10.1039/b602664h
– ident: e_1_2_3_7_2
  doi: 10.1002/ejoc.200500389
– ident: e_1_2_3_43_2
  doi: 10.1021/ol7029799
– ident: e_1_2_3_109_2
  doi: 10.1039/B411438H
– volume-title: Handbook of CH Transformations
  year: 2005
  ident: e_1_2_3_56_3
– ident: e_1_2_3_81_2
  doi: 10.1021/ja055781o
– ident: e_1_2_3_100_2
– start-page: 148
  year: 2006
  ident: e_1_2_3_24_2
  publication-title: ARKIVOC
– ident: e_1_2_3_42_2
  doi: 10.1002/chem.200601016
– ident: e_1_2_3_16_2
– ident: e_1_2_3_33_2
  doi: 10.1021/ja8013743
– ident: e_1_2_3_1_2
– ident: e_1_2_3_32_2
  doi: 10.1002/ange.200462215
– ident: e_1_2_3_60_2
  doi: 10.1016/S0040-4020(02)01563-6
– ident: e_1_2_3_10_2
  doi: 10.1021/ja973524g
– ident: e_1_2_3_104_2
  doi: 10.1039/a707213i
– start-page: 127
  year: 2006
  ident: e_1_2_3_19_2
  publication-title: J. Fluorine Chem.
– ident: e_1_2_3_30_2
  doi: 10.1021/ol047628p
– ident: e_1_2_3_32_3
  doi: 10.1002/anie.200462215
– ident: e_1_2_3_6_2
  doi: 10.1002/tcr.10030
– ident: e_1_2_3_34_2
– ident: e_1_2_3_2_2
  doi: 10.1002/0471212466.ch42
– ident: e_1_2_3_79_2
  doi: 10.1021/jo070625g
– ident: e_1_2_3_112_2
– ident: e_1_2_3_84_2
  doi: 10.1021/ja001205a
– ident: e_1_2_3_18_2
  doi: 10.1246/bcsj.75.1451
– ident: e_1_2_3_105_2
  doi: 10.1016/S0010-8545(98)00215-X
– ident: e_1_2_3_22_2
– ident: e_1_2_3_61_2
  doi: 10.1080/00304940809458089
– volume: 35
  start-page: 1
  year: 1988
  ident: e_1_2_3_85_2
  publication-title: Org. React.
– ident: e_1_2_3_44_2
– ident: e_1_2_3_80_2
  doi: 10.1246/cl.1983.1211
– ident: e_1_2_3_5_2
– start-page: 109
  volume-title: Topics in Organometallic Chemistry, Vol. 14
  year: 2005
  ident: e_1_2_3_64_2
– ident: e_1_2_3_73_2
  doi: 10.1055/s-2005-869966
– ident: e_1_2_3_28_2
  doi: 10.1246/bcsj.76.1055
– ident: e_1_2_3_20_2
  doi: 10.1071/CH07132
– ident: e_1_2_3_26_2
  doi: 10.1055/s-2001-14637
– ident: e_1_2_3_69_2
  doi: 10.1021/jo000535a
– ident: e_1_2_3_103_2
– ident: e_1_2_3_17_2
  doi: 10.1246/cl.1999.45
– ident: e_1_2_3_13_2
– ident: e_1_2_3_67_2
  doi: 10.1021/ja9907111
– ident: e_1_2_3_57_2
– ident: e_1_2_3_54_2
– ident: e_1_2_3_106_2
  doi: 10.1002/(SICI)1521-3749(199804)624:4<737::AID-ZAAC737>3.0.CO;2-L
– ident: e_1_2_3_14_2
  doi: 10.1021/ja005558l
– ident: e_1_2_3_76_2
  doi: 10.1002/ange.200604969
– ident: e_1_2_3_15_2
  doi: 10.1021/jo049385k
– ident: e_1_2_3_114_3
  doi: 10.1002/anie.200460189
– ident: e_1_2_3_101_2
  doi: 10.1021/ja058418q
– ident: e_1_2_3_66_2
  doi: 10.1016/S0040-4039(99)01526-9
– ident: e_1_2_3_99_2
  doi: 10.3762/bjoc.4.10
– ident: e_1_2_3_72_2
  doi: 10.1021/ol048891t
– ident: e_1_2_3_50_2
  doi: 10.1021/ja0362149
– ident: e_1_2_3_96_2
  doi: 10.1021/ol036091x
– ident: e_1_2_3_114_2
  doi: 10.1002/ange.200460189
– ident: e_1_2_3_29_2
  doi: 10.1246/bcsj.77.785
– ident: e_1_2_3_82_2
  doi: 10.1021/om00042a040
– ident: e_1_2_3_41_2
  doi: 10.1002/ange.200605192
– ident: e_1_2_3_45_2
  doi: 10.1021/cr040639b
– ident: e_1_2_3_70_2
  doi: 10.1021/ja011923c
– start-page: 133
  volume-title: Topics in Current Chemistry, Vol. 219
  year: 2002
  ident: e_1_2_3_3_2
– ident: e_1_2_3_25_2
– ident: e_1_2_3_36_2
  doi: 10.1021/jo800266y
– ident: e_1_2_3_88_2
  doi: 10.1039/p19760002285
– ident: e_1_2_3_108_3
  doi: 10.1002/anie.200400655
– ident: e_1_2_3_8_2
– ident: e_1_2_3_86_2
– ident: e_1_2_3_56_2
  doi: 10.1021/cr0509760
– ident: e_1_2_3_76_3
  doi: 10.1002/anie.200604969
– ident: e_1_2_3_41_3
  doi: 10.1002/anie.200605192
– ident: e_1_2_3_98_2
  doi: 10.1021/ja056165v
– ident: e_1_2_3_38_3
  doi: 10.1002/anie.200351923
– ident: e_1_2_3_110_2
  doi: 10.1021/cr030681r
– ident: e_1_2_3_39_2
  doi: 10.1021/ja047472o
– ident: e_1_2_3_107_2
– ident: e_1_2_3_53_2
  doi: 10.1021/ic061997v
– ident: e_1_2_3_77_2
  doi: 10.1016/j.tet.2006.10.071
– start-page: 1250
  year: 2008
  ident: e_1_2_3_21_2
  publication-title: Synlett
– ident: e_1_2_3_38_2
  doi: 10.1002/ange.200351923
– ident: e_1_2_3_59_3
  doi: 10.1002/anie.200390151
– ident: e_1_2_3_92_2
  doi: 10.1021/ol061258i
– ident: e_1_2_3_58_2
  doi: 10.1021/cr990281x
– ident: e_1_2_3_68_2
  doi: 10.1002/(SICI)1521-3757(20000103)112:1<185::AID-ANGE185>3.0.CO;2-N
– ident: e_1_2_3_91_2
– ident: e_1_2_3_55_2
  doi: 10.1039/b515481m
– ident: e_1_2_3_108_2
  doi: 10.1002/ange.200400655
– ident: e_1_2_3_74_2
  doi: 10.1021/ol050859r
– ident: e_1_2_3_37_2
– ident: e_1_2_3_12_3
  doi: 10.1002/anie.200352808
– ident: e_1_2_3_11_2
  doi: 10.1021/jo991342u
– ident: e_1_2_3_63_3
  doi: 10.1002/(SICI)1521-3773(19981016)37:19<2659::AID-ANIE2659>3.0.CO;2-4
– ident: e_1_2_3_78_2
  doi: 10.1002/adsc.200600587
– ident: e_1_2_3_95_2
  doi: 10.1021/ja0264091
– ident: e_1_2_3_111_2
– ident: e_1_2_3_23_2
  doi: 10.1246/cl.2001.526
– ident: e_1_2_3_75_2
  doi: 10.1021/ja0615526
– ident: e_1_2_3_97_2
– ident: e_1_2_3_93_2
  doi: 10.1021/jo800847h
– ident: e_1_2_3_63_2
  doi: 10.1002/(SICI)1521-3757(19981002)110:19<2804::AID-ANGE2804>3.0.CO;2-2
– ident: e_1_2_3_52_2
  doi: 10.1021/ja0680562
– ident: e_1_2_3_94_2
  doi: 10.1039/b801870g
– ident: e_1_2_3_47_2
  doi: 10.1021/ja027683y
– ident: e_1_2_3_51_2
  doi: 10.1021/ja051181d
– ident: e_1_2_3_71_2
  doi: 10.1002/ange.200453809
– ident: e_1_2_3_62_2
– ident: e_1_2_3_65_2
– ident: e_1_2_3_83_2
  doi: 10.1055/s-2006-951516
– ident: e_1_2_3_68_3
  doi: 10.1002/(SICI)1521-3773(20000103)39:1<173::AID-ANIE173>3.0.CO;2-F
– ident: e_1_2_3_113_2
  doi: 10.1021/ol702584t
– ident: e_1_2_3_59_2
  doi: 10.1002/ange.200390119
– ident: e_1_2_3_48_2
  doi: 10.1021/ol800080w
– ident: e_1_2_3_71_3
  doi: 10.1002/anie.200453809
– ident: e_1_2_3_4_2
  doi: 10.1002/adsc.200505158
– ident: e_1_2_3_102_2
  doi: 10.1021/ol0611954
– ident: e_1_2_3_46_2
  doi: 10.1039/B607474J
– ident: e_1_2_3_40_2
  doi: 10.1021/ol062022h
– ident: e_1_2_3_89_2
  doi: 10.1021/jo010162t
– ident: e_1_2_3_35_2
  doi: 10.1021/ol061755z
– ident: e_1_2_3_9_2
  doi: 10.1016/S0040-4039(97)01465-2
– ident: e_1_2_3_12_2
  doi: 10.1002/ange.200352808
– ident: e_1_2_3_27_2
  doi: 10.1246/cl.2002.606
– ident: e_1_2_3_31_2
  doi: 10.1021/ol070900l
– ident: e_1_2_3_87_2
  doi: 10.1021/jo01348a046
– ident: e_1_2_3_49_2
  doi: 10.1016/S0040-4039(00)61007-9
– volume: 128
  start-page: 1066
  year: 2006
  ident: WOS:000234941100017
  article-title: Proton abstraction mechanism for the palladium-catalyzed intramolecular arylation
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja056165v
– start-page: 1250
  year: 2008
  ident: WOS:000256803100033
  article-title: Palladium-catalyzed amino-Heck reaction of γ,δ-unsaturated ketone O-diethylphosphinyloximes:: A new synthesis of substituted pyrroles and indoles
  publication-title: SYNLETT
  doi: 10.1055/s-2008-1072728
– volume: 130
  start-page: 6918
  year: 2008
  ident: WOS:000256301200013
  article-title: A simple, modular synthesis of substituted pyridines
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja8013743
– volume: 124
  start-page: 8348
  year: 2002
  ident: WOS:000176843200030
  article-title: Preparation of benzyne complexes of group 10 metals by intramolecular suzuki coupling of ortho-metalated phenylboronic esters:: Molecular structure of the first benzyne-palladium(0) complex
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0264091
– volume: 46
  start-page: 1910
  year: 2007
  ident: WOS:000244798800006
  article-title: Palladium-catalyzed aerobic oxidative amination of alkenes: Development of intra- and intermolecular Aza-Wacker reactions
  publication-title: INORGANIC CHEMISTRY
  doi: 10.1021/ic061997v
– volume: 8
  start-page: 3347
  year: 2006
  ident: WOS:000239001500048
  article-title: Metal-catalyzed cotrimerization of arynes and alkenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol0611954
– volume: 66
  start-page: 3646
  year: 2001
  ident: WOS:000168907700063
  article-title: Unusual 1,4-addition of 2-pyridyl carboxylates to benzynes: A convenient route to 1-(2-acylphenyl)-2-pyridones
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo010162t
– volume: 43
  start-page: 2436
  year: 2004
  ident: WOS:000221307200024
  article-title: Arylnaphthalene lignans through Pd-catalyzed [2+2+2] cocyclization of arynes and diynes: Total synthesis of taiwanins C and E
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200453809
– volume: 46
  start-page: 3291
  year: 2007
  ident: WOS:000246282900020
  article-title: Palladium-catalyzed three-component synthesis of 3-(diarylmethylene)oxindoles through a domino Sonagashira/carbopalladation/C-H activation/C-C bond-forming sequence
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200605192
– volume: 40
  start-page: 7533
  year: 1999
  ident: WOS:000082964100023
  article-title: Palladium catalyzed co-trimerization of benzyne with alkynes. A facile method for the synthesis of phenanthrene derivatives
  publication-title: TETRAHEDRON LETTERS
– volume: 43
  start-page: 343
  year: 2004
  ident: WOS:000188213300016
  article-title: N-trialkylsilylimines as coupling partners for Pd-catalyzed C-N bond-forming reactions:: One-step synthesis of imines and azadienes from aryl and alkenyl bromides
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200352808
– volume: 75
  start-page: 1451
  year: 2002
  ident: WOS:000177224900004
  article-title: Synthesis of pyrrole derivatives by palladium-catalyzed cyclization of γδ-unsaturated ketone O-pentafluorobenzoyloximes
  publication-title: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
– start-page: 2992
  year: 2008
  ident: WOS:000257236600005
  article-title: O-Dihaloarenes as aryne precursors for nickel-catalyzed [2+2+2]cycloaddition with alkynes and nitriles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b801870g
– volume: 9
  start-page: 2665
  year: 2007
  ident: WOS:000247599400015
  article-title: Asymmetric hydroformylation of vinyl acetate: Application in the synthesis of optically active isoxazolines and imidazoles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol070900l
– start-page: 45
  year: 1999
  ident: WOS:000078361400023
  article-title: Synthesis of pyrrole derivatives by the Heck-type cyclization of γ,δ-unsaturated ketone O-pentafluorobenzoyloximes
  publication-title: CHEMISTRY LETTERS
– start-page: 526
  year: 2001
  ident: WOS:000169538700024
  article-title: Synthesis of pyridine and isoquinoline derivatives by the palladium-catalyzed cyclization of olefinic ketone O-pentafluorobenzoyloximes
  publication-title: CHEMISTRY LETTERS
– volume: 43
  start-page: 6250
  year: 2004
  ident: WOS:000225575600006
  article-title: Controlled microwave heating in modern organic synthesis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200400655
– volume: 119
  start-page: 3355
  year: 2007
  ident: WOS:000262539800023.68
  publication-title: ANGEW CHEM
– start-page: 2285
  year: 1976
  ident: WOS:A1976CM84600014
  article-title: 1,3-DIPOLAR CHARACTER OF 6-MEMBERED AROMATIC RINGS .16. REACTIONS OF BENZYNE WITH 3-HYDROXYPYRIDINE, 1-METHYL-3-OXIDOPYRIDINIUM, AND RELATED COMPOUNDS
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1
– volume: 39
  start-page: 173
  year: 2000
  ident: WOS:000084700400019
  article-title: Palladium-catalyzed intermolecular controlled insertion of benzyne-benzyne-alkene and benzyne-alkyne-alkene - Synthesis of phenanthrene and naphthalene derivatives
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
– volume: 116
  start-page: 347
  year: 2004
  ident: WOS:000262539800023.4
  publication-title: ANGEW CHEM
– volume: 8
  start-page: 4351
  year: 2006
  ident: WOS:000240339700045
  article-title: Rapid access to oxindoles by the combined use of an Ugi four-component reaction and a microwave-assisted intramolecular Buchwald-Hartwig amidation reaction
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol061755z
– volume: 69
  start-page: 5342
  year: 2004
  ident: WOS:000223008100024
  article-title: Palladium-catalyzed transformation of cyclobutanone O-benzoyloximes to nitriles via C-C bond cleavage
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo049385k
– volume: 105
  start-page: 2873
  year: 2005
  ident: WOS:000230522900006
  article-title: Synthesis and functionalization of Indoles through palladium-catalyzed reactions
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr040639b
– volume: 125
  start-page: 12996
  year: 2003
  ident: WOS:000186123900005
  article-title: Dioxygen-coupled oxidative amination of styrene
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0362149
– volume: 126
  start-page: 14475
  year: 2004
  ident: WOS:000224964500049
  article-title: Palladium- and copper-catalyzed synthesis of medium- and large-sized ring-fused dihydroazaphenanthrenes and 1,4-benzodiazepine-2,5-diones. Control of reaction pathway by metal-switching
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja047472o
– volume: 120
  start-page: 827
  year: 1998
  ident: WOS:000071889300030
  article-title: Palladium-catalyzed C-N(sp2) bond formation:: N-arylation of aromatic and unsaturated nitrogen and the reductive elimination chemistry of palladium azolyl and methyleneamido complexes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 5
  start-page: 4875
  year: 2003
  ident: WOS:000187038300031
  article-title: Ultrafast chemistry: Cobalt carbonyl-mediated synthesis of diaryl ketones under microwave irradiation
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol036091x
– volume: 40
  start-page: 215
  year: 2008
  ident: WOS:000256822100001
  article-title: Recent applications of aryne chemistry to organic synthesis. A review
  publication-title: ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL
– volume: 65
  start-page: 169
  year: 2000
  ident: WOS:000084816300026
  article-title: Palladium-catalyzed N-arylation of sulfoximines with aryl bromides and aryl iodides
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 65
  start-page: 6944
  year: 2000
  ident: WOS:000165199000019
  article-title: Selective palladium-catalyzed cocyclotrimerization of arynes with dimethyl acetylenedicarboxylate:: A versatile method for the synthesis of polycyclic aromatic hydrocarbons
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 8
  start-page: 3521
  year: 2006
  ident: WOS:000239309900028
  article-title: New light-induced iminyl radical cyclization reactions of acyloximes to isoquinolines
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol061258i
– volume: 348
  start-page: 23
  year: 2006
  ident: WOS:000234964700001
  article-title: Industrial-scale palladium-catalyzed coupling of aryl halides and amines - A personal account
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.200505158
– volume: 181
  start-page: 147
  year: 1999
  ident: WOS:000078163000005
  article-title: Oxime and oximate metal complexes: unconventional synthesis and reactivity
  publication-title: COORDINATION CHEMISTRY REVIEWS
– volume: 44
  start-page: 3462
  year: 2005
  ident: WOS:000229549100022
  article-title: Concise and practical synthesis of latrunculin A by ring-closing enyne-yne metathesis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200500390
– volume: 116
  start-page: 6408
  year: 2004
  ident: WOS:000262539800023.42
  publication-title: ANGEW CHEM
– volume: 110
  start-page: 2804
  year: 1998
  ident: WOS:000262539800023.63
  publication-title: ANGEW CHEM
– volume: 33
  start-page: 6643
  year: 1992
  ident: WOS:A1992JV80200024
  article-title: PALLADIUM(II)-CATALYZED AMIDATION OF ALKENES
  publication-title: TETRAHEDRON LETTERS
– volume: 128
  start-page: 7426
  year: 2006
  ident: WOS:000238099500014
  article-title: Three-component coupling of benzyne: Domino intermolecular carbopalladation
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0615526
– volume: 42
  start-page: 502
  year: 2003
  ident: WOS:000181379500003
  article-title: One century of aryne chemistry
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
– volume: 112
  start-page: 185
  year: 2000
  ident: WOS:000262539800023.97
  publication-title: ANGEW CHEM
– volume: 219
  start-page: 131
  year: 2002
  ident: WOS:000174161500006
  article-title: Practical palladium catalysts for C-N and C-O bond formation
  publication-title: CROSS-COUPLING REACTIONS
– volume: 119
  start-page: 2587
  year: 2007
  ident: WOS:000262539800023.53
  publication-title: ANGEW CHEM
– volume: 63
  start-page: 347
  year: 2007
  ident: WOS:000243662300008
  article-title: Synthesis of carbazoles and dibenzofurans via cross-coupling of o-iodoanilines and o-iodophenols with silylaryl triflates and subsequent Pd-catalyzed cyclization
  publication-title: TETRAHEDRON
  doi: 10.1016/j.tet.2006.10.071
– volume: 14
  start-page: 109
  year: 2005
  ident: CCC:000232634400005
  article-title: Palladium-catalyzed cycloaddition reactions of arynes
  publication-title: PALLADIUM IN ORGANIC SYNTHESIS
– volume: 11
  start-page: 2212
  year: 1992
  ident: WOS:A1992HY67400040
  article-title: FLUORIDE-INDUCED REDUCTION OF PALLADIUM(II) AND PLATINUM(II) PHOSPHINE COMPLEXES
  publication-title: ORGANOMETALLICS
– volume: 60
  start-page: 624
  year: 2007
  ident: WOS:000248651300012
  article-title: Synthesis of 5-phenyl 2-functionalized pyrroles by amino Heck and tandem amino Heck carbonylation reactions
  publication-title: AUSTRALIAN JOURNAL OF CHEMISTRY
  doi: 10.1071/CH07132
– volume: 13
  start-page: 961
  year: 2007
  ident: WOS:000243622500026
  article-title: Palladium-catalyzed enantioselective domino Heck-cyanation sequence: Development and application to the total synthesis of esermethole and physostigmine
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200601016
– volume: 9
  start-page: 5589
  year: 2007
  ident: WOS:000251614900065
  article-title: Biaryl synthesis via palladium-catalyzed aryne multicomponent coupling
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol702584t
– start-page: 974
  year: 2001
  ident: WOS:000169286700022
  article-title: Synthesis of spiro imines from oximes by palladium-catalyzed cascade reaction
  publication-title: SYNLETT
– volume: 107
  start-page: 174
  year: 2007
  ident: WOS:000243381000008
  article-title: Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr0509760
– volume: 6
  start-page: 2821
  year: 2004
  ident: WOS:000223013300046
  article-title: Palladium-catalyzed allylalkynylation of benzynes: A highly efficient route to substituted 1-allyl-2 alkynylbenzenes
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol048891t
– start-page: 606
  year: 2002
  ident: WOS:000176347400026
  article-title: Palladium-catalyzed synthesis of 1-azaazulenes from cycloheptatrienylmethyl ketone O-pentafluorobenzoyl oximes
  publication-title: CHEMISTRY LETTERS
– volume: 72
  start-page: 5431
  year: 2007
  ident: WOS:000247612200058
  article-title: Synthesis of indolo[1,2-f]phenanthridines from palladium-catalyzed reactions of arynes
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo070625g
– volume: 43
  start-page: 5052
  year: 2004
  ident: WOS:000224283900018
  article-title: Distannylation of strained carbon-carbon triple bonds catalysed by a palladium complex
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200460189
– volume: 37
  start-page: 2659
  year: 1998
  ident: WOS:000076575900011
  article-title: Efficient palladium-catalyzed cyclotrimerization of arynes:: Synthesis of triphenylenes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
– volume: 127
  start-page: 489
  year: 2006
  ident: WOS:000237986300005
  article-title: Heck-type 5-endo-trig cyclizations promoted by vinylic fluorines:: Ring-fluorinated indene and 3H-pyrrole syntheses from 1,1-difluoro-1-alkenes
  publication-title: JOURNAL OF FLUORINE CHEMISTRY
  doi: 10.1016/j.jfluchem.2005.12.023
– volume: 4
  start-page: ARTN 10
  year: 2008
  ident: WOS:000256826500001
  article-title: Synthesis of dihydrophenanthridines by a sequence of Ugi-4CR and palladium-catalyzed intramolecular C-H functionalization
  publication-title: BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.3762/bjoc.4.10
– volume: 1
  start-page: 1051
  year: 2002
  ident: WOS:000262539800023.31
  publication-title: HDB ORGANOPALLADIUM
– volume: 10
  start-page: 1179
  year: 2008
  ident: WOS:000254032100036
  article-title: Sequential intermolecular aminopalladation/ortho-arene C-H activation reactions of N-phenylpropiolamides with phthalimide
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol800080w
– volume: 38
  start-page: 6367
  year: 1997
  ident: WOS:A1997XU80200016
  article-title: An ammonia equivalent for the palladium-catalyzed amination of aryl halides and triflates
  publication-title: TETRAHEDRON LETTERS
– start-page: 325
  year: 1998
  ident: WOS:000072111100003
  article-title: The first direct observation of N-O bond cleavage in the oxidative addition of an oxime to a metal centre.: Synthesis and crystal structure of the methyleneamide complex trans-[Re(OH)(N=CMe2)(Ph2PCH2CH2PPh2)2][HSO4]
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
– volume: 35
  start-page: 1
  year: 1988
  ident: WOS:000262539800023.29
  publication-title: ORG REACTIONS
  doi: 10.1002/0471264180.OR035.01
– volume: 77
  start-page: 785
  year: 2004
  ident: WOS:000221089300024
  article-title: Synthesis of 1-azaazulenes from cycloheptatrienylmethyl ketone O-pentafluorobenzoyloximes by palladium-catalyzed cyclization and oxidation
  publication-title: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
  doi: 10.1246/bcsj.77.785
– volume: 129
  start-page: 762
  year: 2007
  ident: WOS:000243683800019
  article-title: A facile Pd(0)-catalyzed regio- and stereoselective diamination of conjugated dienes and trienes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja0680562
– volume: 42
  start-page: 4774
  year: 2003
  ident: WOS:000186128300010
  article-title: One-pot synthesis of polyheterocycles by a palladium-catalyzed intramolecular N-arylation/C-H activation/aryl-aryl bond-forming domino process
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200351923
– volume: 127
  start-page: 7308
  year: 2005
  ident: WOS:000229244600023
  article-title: Pd(II)-catalyzed intermolecular 1,2-diamination of conjugated dienes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja051181d
– volume: 124
  start-page: 12670
  year: 2002
  ident: WOS:000178792400018
  article-title: Palladium-catalyzed intermolecular hydroamination of alkynes:: A dramatic rate-enhancement effect of o-aminophenol
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja027683y
– volume: 7
  start-page: 2921
  year: 2005
  ident: WOS:000230213100030
  article-title: Highly efficient route to o-allylbiaryls via palladium-catalyzed three-component coupling of benzynes, allylic halides, and aryl organometallic reagents
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol050859r
– volume: 121
  start-page: 5827
  year: 1999
  ident: WOS:000081152200037
  article-title: Palladium-catalyzed cocyclization of arynes with alkynes:: Selective synthesis of phenanthrenes and naphthalenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 123
  start-page: 12686
  year: 2001
  ident: WOS:000172745300032
  article-title: Catalytic carbonylation reactions of benzyne derivatives
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja011923c
– volume: 122
  start-page: 7280
  year: 2000
  ident: WOS:000088658400015
  article-title: Palladium-catalyzed controlled carbopalladation of benzyne
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 624
  start-page: 737
  year: 1998
  ident: WOS:000073029100033
  article-title: N-O bond cleavage in O-silylated oximes by reaction with a titanocene-alkyne complex
  publication-title: ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE
– volume: 8
  start-page: 4927
  year: 2006
  ident: WOS:000241030900065
  article-title: Synthesis of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol062022h
– volume: 116
  start-page: 2490
  year: 2004
  ident: WOS:000262539800023.81
  publication-title: ANGEW CHEM
– volume: 100
  start-page: 2901
  year: 2000
  ident: WOS:000088838500007
  article-title: Recent advances in the transition-metal-catalyzed regioselective approaches to polysubstituted benzene derivatives
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr990281x
– start-page: V
  year: 2005
  ident: WOS:000299053100001
  article-title: Handbook of C-H Transformations Applications in Organic Synthesis Volume 1 Preface
  publication-title: HANDBOOK OF C-H TRANSFORMATIONS: APPLICATIONS IN ORGANIC SYNTHESIS, VOL 1
– volume: 128
  start-page: 2232
  year: 2006
  ident: WOS:000235562900039
  article-title: Ene reaction of arynes with alkynes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja058418q
– volume: 349
  start-page: 647
  year: 2007
  ident: WOS:000245379400024
  article-title: Synthesis of biaryls via palladium-catalyzed [2+2+2] cocyclization of arynes and diynes:: Application to the synthesis of arylnaphthalene lignans
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.200600587
– volume: 2
  start-page: 268
  year: 2002
  ident: WOS:000182372900006
  article-title: Synthesis of aza-heterocycles from oximes by amino-Heck reaction
  publication-title: CHEMICAL RECORD
  doi: 10.1002/tcr.10030
– volume: 46
  start-page: 2535
  year: 2007
  ident: WOS:000245371300040
  article-title: Palladium-catalyzed, sequential, three-component cross-coupling of aryl halides, alkynes, and arynes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.200604969
– volume: 59
  start-page: 701
  year: 2003
  ident: WOS:000180777200001
  article-title: The use of arynes in organic synthesis
  publication-title: TETRAHEDRON
– volume: 127
  start-page: 15716
  year: 2005
  ident: WOS:000233535400028
  article-title: Synthesis of fused polycyclic aromatics by palladium-catalyzed annulation of arynes using 2-halobiaryls
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja055781o
– start-page: 148
  year: 2006
  ident: WOS:000237240500013
  article-title: Palladium(0)-catalyzed synthesis of pyridines from β-acetoxy-γ,δ-unsaturated ketone oximes
  publication-title: ARKIVOC
– volume: 7
  start-page: 609
  year: 2005
  ident: WOS:000226950100022
  article-title: Synthesis of trisubstituted imidazoles by palladium-catalyzed cyclization of O-pentafluorobenzoylamidoximes:: Application to amino acid mimetics with a C-terminal imidazole
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol047628p
– volume: 31
  start-page: 3307
  year: 1966
  ident: WOS:A19668354300046
  article-title: ARYNES BY PYROLYSIS OF ACID ANHYDRIDES
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 115
  start-page: 4922
  year: 2003
  ident: WOS:000262539800023.16
  publication-title: ANGEW CHEM
– start-page: 2454
  year: 2006
  ident: WOS:000238101100007
  article-title: Reaction of arynes, N-heteroaromatics and nitriles
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/b602664h
– volume: 122
  start-page: 12049
  year: 2000
  ident: WOS:000165696900058
  article-title: Palladium(0)-catalyzed ring cleavage of cyclobutanone grimes leading to nitriles via β-carbon elimination
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 76
  start-page: 1055
  year: 2003
  ident: WOS:000183391700024
  article-title: Synthesis of polycyclic Imines by palladium-catalyzed domino cyclization of Di- and trienyl ketone O-pentafluorobenzoyloximes
  publication-title: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
– volume: 34
  start-page: 164
  year: 2005
  ident: WOS:000226522500006
  article-title: Microwaves in organic synthesis.: Thermal and non-thermal microwave effects
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/b411438h
– volume: 36
  start-page: 1142
  year: 2007
  ident: WOS:000247341300011
  article-title: Intramolecular aminopalladation of alkenes as a key step to pyrrolidines and related heterocycles
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/b607474j
– start-page: 1253
  year: 2006
  ident: WOS:000236004300001
  article-title: Palladium-catalyzed direct arylation of simple arenes in synthesis of biaryl molecules
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/B515481M
– volume: 115
  start-page: 518
  year: 2003
  ident: WOS:000262539800023.93
  publication-title: ANGEW CHEM
– start-page: 1693
  year: 2005
  ident: WOS:000230380900024
  article-title: Substituted 1-allyl-2-allenylbenzenes via palladium-catalyzed allylallenylation of benzyne derivatives
  publication-title: SYNTHESIS-STUTTGART
  doi: 10.1055/s-2005-869966
– volume: 73
  start-page: 3600
  year: 2008
  ident: WOS:000255339600044
  article-title: Palladium-catalyzed intramolecular C-arylation of benzylic carbon:: Synthesis of 3-benzoxazolylisoindolinones by a sequence of Ugi-4CR/postfunctionalization
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo800266y
– volume: 73
  start-page: 5558
  year: 2008
  ident: WOS:000257543100044
  article-title: Microwave-assisted syntheses of n-heterocycles using alkenone-, alkynone- and aryl-carbonyl O-phenyl oximes:: Formal synthesis of neocryptolepine
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/jo800847h
– volume: 105
  start-page: 2527
  year: 2005
  ident: WOS:000229729000017
  article-title: The potential of palladacycles: More than just precatalysts
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr030681r
– start-page: 2921
  year: 2006
  ident: WOS:000243619600008
  article-title: Reduction of allylpalladium(II)chloride dimer by formation of allyloxysilanes
  publication-title: SYNLETT
  doi: 10.1055/s-2006-951516
– volume: 10
  start-page: 857
  year: 2008
  ident: WOS:000253519600044
  article-title: Palladium-catalyzed domino intramolecular N-arylation/intermolecular C-C bond formation for the synthesis of functionalized benzodiazepinediones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol7029799
– volume: 2005
  start-page: 4505
  year: 2005
  ident: WOS:000233144000002
  article-title: Amination with oximes
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.200500389
– start-page: 1211
  year: 1983
  ident: WOS:A1983RB99500022
  article-title: FLUORIDE-INDUCED 1,2-ELIMINATION OF ORTHO-TRIMETHYLSILYLPHENYL TRIFLATE TO BENZYNE UNDER MILD CONDITIONS
  publication-title: CHEMISTRY LETTERS
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Snippet Intermolecular insertion: A palladium‐catalyzed domino aminopalladation/ CH functionalization sequence has been developed, and provides access to...
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SubjectTerms arynes
Cellular Biology
Chemistry
Chemistry, Multidisciplinary
domino reactions
heterocycles
Life Sciences
oximes
palladium
Physical Sciences
Science & Technology
Title Palladium-Catalyzed Annulation of Acyloximes with Arynes (or Alkynes): Synthesis of Phenanthridines and Isoquinolines
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.200804683
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https://www.ncbi.nlm.nih.gov/pubmed/19067452
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Volume 48
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