Vinyl‐/Furoindoles and Gold Catalysis: New Achievements and Future Perspectives for the Synthesis of Complex Indole Derivatives
The reactivity of vinyl‐/furoindole derivatives with gold‐activated π‐systems is the subject of extensive investigation. In the presence of these electrophilic partners, the realized transformations allow for the construction of different and fascinating architectures via cycloaddition and cyclizati...
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| Published in | European journal of inorganic chemistry Vol. 2020; no. 11-12; pp. 962 - 977 |
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| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
Wiley Subscription Services, Inc
27.03.2020
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1434-1948 1099-0682 |
| DOI | 10.1002/ejic.201901044 |
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| Abstract | The reactivity of vinyl‐/furoindole derivatives with gold‐activated π‐systems is the subject of extensive investigation. In the presence of these electrophilic partners, the realized transformations allow for the construction of different and fascinating architectures via cycloaddition and cyclization reactions often included in cascade processes. The reactions realized involving in these processes an external substituent at the indole moiety are the subject of the present minireview.
The use of substituted or polycyclic indoles in reactions with gold‐activated π‐systems allows for the synthesis of new classes of carbazole derivatives and highly functionalized indoles under mild conditions and with high level of regio diastereo and enantio selectivities. |
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| AbstractList | The reactivity of vinyl‐/furoindole derivatives with gold‐activated π‐systems is the subject of extensive investigation. In the presence of these electrophilic partners, the realized transformations allow for the construction of different and fascinating architectures via cycloaddition and cyclization reactions often included in cascade processes. The reactions realized involving in these processes an external substituent at the indole moiety are the subject of the present minireview.
The use of substituted or polycyclic indoles in reactions with gold‐activated π‐systems allows for the synthesis of new classes of carbazole derivatives and highly functionalized indoles under mild conditions and with high level of regio diastereo and enantio selectivities. The reactivity of vinyl‐/furoindole derivatives with gold‐activated π‐systems is the subject of extensive investigation. In the presence of these electrophilic partners, the realized transformations allow for the construction of different and fascinating architectures via cycloaddition and cyclization reactions often included in cascade processes. The reactions realized involving in these processes an external substituent at the indole moiety are the subject of the present minireview. |
| Author | Abbiati, Giorgio Rossi, Elisabetta Brambilla, Elisa Pirovano, Valentina |
| Author_xml | – sequence: 1 givenname: Valentina orcidid: 0000-0003-3113-6579 surname: Pirovano fullname: Pirovano, Valentina organization: Dipartimento di Scienze Farmaceutiche – sequence: 2 givenname: Giorgio orcidid: 0000-0002-2502-4127 surname: Abbiati fullname: Abbiati, Giorgio organization: Dipartimento di Scienze Farmaceutiche – sequence: 3 givenname: Elisa orcidid: 0000-0001-5992-4361 surname: Brambilla fullname: Brambilla, Elisa organization: Dipartimento di Scienze Farmaceutiche – sequence: 4 givenname: Elisabetta orcidid: 0000-0003-0397-6175 surname: Rossi fullname: Rossi, Elisabetta email: elisabetta.rossi@unimi.it organization: Dipartimento di Scienze Farmaceutiche |
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| Cites_doi | 10.1002/ange.201710105 10.1002/ejoc.201700453 10.1002/anie.201107575 10.1002/ejoc.200600625 10.1021/ja905415r 10.1021/acs.orglett.5b02663 10.1021/cr078361l 10.1039/C0CC04164E 10.1016/j.ejmech.2013.06.012 10.1039/9781782623717-00001 10.1016/j.tetasy.2010.06.011 10.1002/adsc.201700280 10.1039/C5CS00929D 10.2533/chimia.2018.610 10.1002/9781118778173.ch13 10.1021/acscatal.6b02446 10.1002/ange.200901843 10.1002/adsc.200600294 10.1021/ja074824t 10.1021/ja807243t 10.1016/S0040-4039(00)96520-1 10.1021/ja005570d 10.1002/jhet.5570160435 10.1002/anie.201404029 10.1002/ange.200906550 10.1007/128_2014_589 10.1021/ol202046y 10.1039/C4CC04633A 10.1002/cctc.201200224 10.1002/ejoc.201700120 10.1021/acs.joc.9b00143 10.1016/j.jorganchem.2019.06.032 10.1021/ja1095045 10.1002/anie.201405381 10.1002/chem.201503598 10.1002/ijch.201300040 10.1039/C6QO00087H 10.1039/c3cc41514g 10.1039/C9QO00647H 10.1039/C4CC08736D 10.1021/acs.orglett.7b01868 10.1016/B978-0-08-095167-6.00222-6 10.1002/ange.200907078 10.1002/anie.200704566 10.1021/ja200084a 10.1039/C6CC04474C 10.1039/C3CC45518A 10.1039/C1OB06604H 10.1039/b907043e 10.1039/c0cc03621h 10.1002/ejoc.201800125 10.1002/chem.201100260 10.1016/B978-0-12-408100-0.00001-X 10.1021/jo070579k 10.1039/C6CC00633G 10.1002/chem.200900164 10.1039/C4QO00130C 10.1002/ejoc.201403580 10.1002/ejoc.201300725 10.1016/j.tetlet.2013.10.036 10.1021/ja901649s 10.1002/cnma.201800132 10.1021/jacs.6b01008 10.1002/jhet.5570140605 10.1002/ijch.201300029 10.1016/j.tet.2007.07.068 10.1002/chem.201602822 10.1055/s-0035-1561638 10.1021/cr078346g 10.1021/ar400188g 10.1002/ange.201404029 10.1002/ange.200802517 10.1021/ar4001839 10.1021/ja062707c 10.1055/s-0032-1317588 10.1007/s10562-014-1400-8 10.1002/ejoc.201500878 10.1002/adsc.201000644 10.1021/ja3065446 10.1021/cs400922y 10.1039/C7OB00413C 10.1021/jacs.7b07531 10.1351/PAC-CON-11-09-05 10.1039/C5SC01827G 10.1002/chem.201402500 10.1055/s-2005-918509 10.1002/anie.200907078 10.1007/BF00506385 10.1039/c0cc03620j 10.1246/cl.131230 10.1039/c3cs60441a 10.1002/adsc.201500913 10.1021/acs.accounts.8b00625 10.1021/jm00161a026 10.1021/acs.accounts.9b00144 10.1039/c2cs15333e 10.1002/anie.200901843 10.1002/9783527646869.ch4 10.1021/acs.orglett.9b02085 10.1021/ar4002558 10.1002/chem.201601129 10.1021/acs.orglett.6b00191 10.1021/acs.accounts.8b00567 10.1002/anie.200906550 10.1002/adsc.201000597 10.1515/pac-2016-0101 10.1002/jhet.5570150126 10.1002/cctc.201000413 10.3762/bjoc.7.124 10.1002/anie.200802517 10.1002/ange.201405381 10.1039/c2cc33030j 10.1039/c0sc00630k 10.1002/chem.201700727 10.1002/jlac.199019900185 10.1002/ange.201107575 10.1002/anie.201710105 10.1002/ange.200704566 |
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| References | 2015; 6 2011; 2 2019; 6 2013; 49 2017 2016 2016 2014 2013 2012 2012 2012 2018 2015 2014 2014 2012; 2017 27 88 43 53 84 51 124 72 357 47 47 2015; 51 2009 2009 2017 2018; 48 121 15 2018 2019 2016 2015; 52 52 145 2009 2008; 108 2019 2014 2014; 52 43 2001 2015; 5 2015 2006 2019 2016 2015 2014 2014 2012; 897 18 17 53 126 48 2010 2010; 49 122 2011; 3 2014 2013 2019; 110 21 2011; 7 2011; 353 2012 2014; 4 2011; 133 2019 2018 2016 2017 2016; 52 4 3 23 6 2017; 359 2017; 139 2014; 20 2014; 1 2007 2012 2013; 2007 23 2013 2013 1986; 66 29 2012; 134 2019; 84 2016; 3 2015 2016 2017; 138 2017 2007 2011 2007 2010; 72 133 129 21 2015; 21 2008 2008 2000; 47 120 122 2018 2018 2017 2014 2014 2014 2013 2012 2011 2016 2014; 57 130 23 50 771 55 53 4 22 47 2006 2010 2010 2011 2012 2017; 348 46 46 17 10 19 2016; 358 2009 2009 2008 2008 2010 2010 2009; 131 15 47 120 49 122 131 2008 2008 2011 2016; 108 130 13 52 2011; 47 1984 2014 2014; 20 53 126 1977 1978 1979 2007; 14 15 16 63 2014; 50 2006; 128 1987 1990; 28 2012; 41 2016; 45 e_1_2_6_30_1 e_1_2_6_19_1 e_1_2_6_34_3 e_1_2_6_34_2 e_1_2_6_11_1 e_1_2_6_34_1 e_1_2_6_34_6 e_1_2_6_15_1 e_1_2_6_34_5 e_1_2_6_38_1 e_1_2_6_34_4 e_1_2_6_41_1 e_1_2_6_9_1 e_1_2_6_5_4 e_1_2_6_9_3 e_1_2_6_9_2 e_1_2_6_5_1 Munoz M. P. (e_1_2_6_13_2) 2014 e_1_2_6_5_3 e_1_2_6_5_2 e_1_2_6_49_1 e_1_2_6_22_1 e_1_2_6_45_1 e_1_2_6_45_2 e_1_2_6_26_1 e_1_2_6_45_3 e_1_2_6_50_2 e_1_2_6_50_3 e_1_2_6_50_4 e_1_2_6_50_5 e_1_2_6_31_2 e_1_2_6_31_1 e_1_2_6_50_1 e_1_2_6_35_2 e_1_2_6_35_1 e_1_2_6_12_1 e_1_2_6_39_1 e_1_2_6_16_1 e_1_2_6_35_3 e_1_2_6_3_13 e_1_2_6_42_1 e_1_2_6_3_10 e_1_2_6_3_11 e_1_2_6_3_12 e_1_2_6_2_4 e_1_2_6_2_3 e_1_2_6_21_11 e_1_2_6_21_10 e_1_2_6_6_1 Najera C. (e_1_2_6_21_5) 2014; 771 e_1_2_6_2_2 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_27_1 e_1_2_6_46_1 e_1_2_6_46_2 e_1_2_6_51_1 e_1_2_6_51_2 e_1_2_6_51_3 e_1_2_6_51_4 e_1_2_6_32_1 e_1_2_6_13_1 e_1_2_6_36_1 Pradal A. (e_1_2_6_21_9) 2011 e_1_2_6_32_4 e_1_2_6_32_3 e_1_2_6_32_2 e_1_2_6_17_1 e_1_2_6_51_5 e_1_2_6_51_6 e_1_2_6_13_3 e_1_2_6_13_4 e_1_2_6_43_1 e_1_2_6_20_2 e_1_2_6_20_1 Butin A. V. (e_1_2_6_37_1) 2001; 5 e_1_2_6_3_7 e_1_2_6_3_6 e_1_2_6_3_9 e_1_2_6_3_8 e_1_2_6_3_3 e_1_2_6_3_2 e_1_2_6_3_5 e_1_2_6_7_1 e_1_2_6_3_4 e_1_2_6_47_2 e_1_2_6_24_1 e_1_2_6_3_1 e_1_2_6_28_1 e_1_2_6_47_1 e_1_2_6_10_1 e_1_2_6_14_6 e_1_2_6_18_2 e_1_2_6_14_7 e_1_2_6_14_1 e_1_2_6_33_3 e_1_2_6_33_2 e_1_2_6_33_1 e_1_2_6_14_4 e_1_2_6_14_5 e_1_2_6_18_1 e_1_2_6_14_2 e_1_2_6_37_2 e_1_2_6_14_3 e_1_2_6_21_1 e_1_2_6_40_1 e_1_2_6_8_2 e_1_2_6_8_1 e_1_2_6_8_4 e_1_2_6_8_3 e_1_2_6_4_2 e_1_2_6_4_1 e_1_2_6_4_3 e_1_2_6_25_1 e_1_2_6_48_1 e_1_2_6_21_4 e_1_2_6_48_2 e_1_2_6_21_3 e_1_2_6_48_3 e_1_2_6_21_2 e_1_2_6_29_1 e_1_2_6_44_1 e_1_2_6_21_8 e_1_2_6_21_7 e_1_2_6_21_6 |
| References_xml | – volume: 66 29 start-page: 466 2284 year: 2013 1986 end-page: 479 2290 publication-title: Eur. J. Med. Chem J. Med. Chem – volume: 20 start-page: 13174 year: 2014 end-page: 13180 publication-title: Chem. Eur. J – volume: 41 start-page: 3511 year: 2012 end-page: 3522 publication-title: Chem. Soc. Rev – volume: 358 start-page: 403 year: 2016 end-page: 409 publication-title: Adv. Synth. Catal – volume: 3 start-page: 759 year: 2016 end-page: 763 publication-title: Org. Chem. Front – volume: 128 start-page: 8418 year: 2006 end-page: 8420 publication-title: J. Am. Chem. Soc – volume: 2017 27 88 43 53 84 51 124 72 357 47 47 start-page: 4512 2039 207 572 856 1673 46 46 610 25 939 966 685 year: 2017 2016 2016 2014 2013 2012 2012 2012 2018 2015 2014 2014 2012 end-page: 4529 2042 214 578 868 1684 48 613 62 952 977 737 publication-title: Eur. J. Org. Chem Synlett Pure Appl. Chem Chem. Lett Isr. J. Chem Pure Appl. Chem Angew. Chem. Int. Ed Angew. Chem Chimia Top. Curr. Chem Acc. Chem. Res Acc. Chem. Res – volume: 52 43 start-page: 465 567 2941 year: 2019 2014 2014 end-page: 479 630 2955 publication-title: Acc. Chem. Res Chem. Soc. Rev – volume: 133 start-page: 5500 year: 2011 end-page: 5507 publication-title: J. Am. Chem. Soc – volume: 6 start-page: 5564 year: 2015 end-page: 5570 publication-title: Chem. Sci – volume: 50 start-page: 16 year: 2014 end-page: 28 publication-title: Chem. Commun – volume: 353 start-page: 392 year: 2011 end-page: 400 publication-title: Adv. Synth. Catal – volume: 28 start-page: 4397 449 year: 1987 1990 end-page: 4398 452 publication-title: Tetrahedron Lett Liebigs Ann. Chem – volume: 47 start-page: 1887 year: 2011 end-page: 1889 publication-title: Chem. Commun – volume: 6 start-page: 3078 year: 2019 end-page: 3084 publication-title: Org. Chem. Front – volume: 110 21 start-page: 355 1 6231 year: 2014 2013 2019 end-page: 406 41 6234 publication-title: Adv. Heterocycl. Chem Org. Lett – volume: 1 start-page: 759 year: 2014 end-page: 764 publication-title: Org. Chem. Front – volume: 2 start-page: 633 year: 2011 end-page: 637 publication-title: Chem. Sci – volume: 52 4 3 23 6 start-page: 1565 720 1 9439 7979 year: 2019 2018 2016 2017 2016 end-page: 1574 729 30 9450 7988 publication-title: Acc. Chem. Res ChemNanoMat Nanoscience Chem. Eur. J ACS Catal – volume: 21 start-page: 18445 year: 2015 end-page: 18453 publication-title: Chem. Eur. J – volume: 4 start-page: 75 1911 year: 2012 2014 end-page: 134 1925 publication-title: ACS Catal – volume: 57 130 23 50 771 55 53 4 22 47 start-page: 386 392 467 15124 78 577 848 1065 1501 6803 889 year: 2018 2018 2017 2014 2014 2014 2013 2012 2011 2016 2014 end-page: 388 512 15135 92 584 855 1066 1514 6807 901 publication-title: Angew. Chem. Int. Ed Angew. Chem Chem. Eur. J Chem. Commun J. Organomet. Chem Tetrahedron Lett Isr. J. Chem ChemCatChem Synthesis Chem. Eur. J Acc. Chem. Res – volume: 49 122 start-page: 5232 5360 year: 2010 2010 end-page: 5241 publication-title: Angew. Chem. Int. Ed Angew. Chem – volume: 7 start-page: 1075 year: 2011 end-page: 1094 publication-title: Beilstein J. Org. Chem – volume: 134 start-page: 14322 year: 2012 end-page: 14325 publication-title: J. Am. Chem. Soc – volume: 52 52 145 start-page: 576 11038 220 year: 2019 2016 2015 end-page: 584 11051 232 publication-title: Acc. Chem. Res Chem. Commun Catal. Lett – volume: 5 2015 start-page: 131 2999 year: 2001 2015 end-page: 168 3016 publication-title: Targets Heterocycl. Syst Eur. J. Org. Chem – volume: 84 start-page: 5150 year: 2019 end-page: 5166 publication-title: J. Org. Chem – volume: 2007 23 2013 start-page: 517 2913 6267 year: 2007 2012 2013 end-page: 525 2918 6279 publication-title: Eur. J. Org. Chem Synlett Eur. J. Org. Chem – volume: 897 18 17 53 126 48 start-page: 70 1072 5124 14022 14246 7200 year: 2019 2016 2015 2014 2014 2012 end-page: 79 1075 5127 14026 7202 publication-title: J. Organomet. Chem Org. Lett Org. Lett Angew. Chem. Int. Ed Angew. Chem Chem. Commun – volume: 3 start-page: 647 year: 2011 end-page: 648 publication-title: ChemCatChem – start-page: 299 year: 2006 end-page: 304 publication-title: Synthesis – volume: 108 start-page: 5359 year: 2008 end-page: 5406 publication-title: Chem. Rev – start-page: 7113 year: 2009 end-page: 7120 publication-title: Dalton Trans – volume: 51 start-page: 2320 year: 2015 end-page: 2323 publication-title: Chem. Commun – volume: 14 15 16 63 start-page: 975 123 785 10320 year: 1977 1978 1979 2007 end-page: 979 125 788 10329 publication-title: J. Heterocycl. Chem J. Heterocycl. Chem J. Heterocycl. Chem Tetrahedron – volume: 138 2017 start-page: 6146 3998 4011 year: 2015 2016 2017 end-page: 6151 4001 4025 publication-title: Eur. J. Org. Chem J. Am. Chem. Soc Eur. J. Org. Chem – volume: 359 start-page: 1912 year: 2017 end-page: 1918 publication-title: Adv. Synth. Catal – volume: 45 start-page: 4567 year: 2016 end-page: 4589 publication-title: Chem. Soc. Rev – volume: 49 start-page: 3594 year: 2013 end-page: 3596 publication-title: Chem. Commun – volume: 348 46 46 17 10 19 start-page: 2297 8886 8904 3812 699 4106 year: 2006 2010 2010 2011 2012 2017 end-page: 2306 8903 8922 3822 704 4109 publication-title: Adv. Synth. Catal Chem. Commun Chem. Commun Chem. Eur. J Org. Biomol. Chem Org. Lett – volume: 20 53 126 start-page: 951 10232 10397 year: 1984 2014 2014 end-page: 957 10236 publication-title: Chem. Heterocycl. Compd Angew. Chem. Int. Ed Angew. Chem – volume: 72 133 129 21 start-page: 7817 3517 12638 1184 year: 2007 2011 2007 2010 end-page: 7831 3527 12639 1186 publication-title: J. Org. Chem J. Am. Chem. Soc J. Am. Chem. Soc Tetrahedron: Asymmetry – volume: 108 130 13 52 start-page: 3174 17961 5172 4581 year: 2008 2008 2011 2016 end-page: 3198 17969 5175 4584 publication-title: Chem. Rev J. Am. Chem. Soc Org. Lett Chem. Commun – volume: 131 15 47 120 49 122 131 start-page: 6348 3336 951 965 1949 1993 13020 year: 2009 2009 2008 2008 2010 2010 2009 end-page: 6349 3339 954 1953 13030 publication-title: J. Am. Chem. Soc Chem. Eur. J Angew. Chem. Int. Ed Angew. Chem Angew. Chem. Int. Ed Angew. Chem J. Am. Chem. Soc – volume: 353 start-page: 550 year: 2011 end-page: 556 publication-title: Adv. Synth. Catal – volume: 47 120 122 start-page: 2285 6856 11553 year: 2008 2008 2000 end-page: 2288 11554 publication-title: Angew. Chem. Int. Ed Angew. Chem J. Am. Chem. Soc – volume: 48 121 15 2018 start-page: 9608 9786 3550 1925 year: 2009 2009 2017 2018 end-page: 9644 3567 1945 publication-title: Angew. Chem. Int. Ed Angew. Chem Org. Biomol. Chem Eur. J. Org. Chem – volume: 139 start-page: 15060 year: 2017 end-page: 15067 publication-title: J. Am. Chem. Soc. – ident: e_1_2_6_21_2 doi: 10.1002/ange.201710105 – ident: e_1_2_6_35_3 doi: 10.1002/ejoc.201700453 – ident: e_1_2_6_3_7 doi: 10.1002/anie.201107575 – ident: e_1_2_6_4_1 doi: 10.1002/ejoc.200600625 – ident: e_1_2_6_14_7 doi: 10.1021/ja905415r – ident: e_1_2_6_51_3 doi: 10.1021/acs.orglett.5b02663 – ident: e_1_2_6_8_1 doi: 10.1021/cr078361l – ident: e_1_2_6_38_1 doi: 10.1039/C0CC04164E – ident: e_1_2_6_31_1 doi: 10.1016/j.ejmech.2013.06.012 – ident: e_1_2_6_50_3 doi: 10.1039/9781782623717-00001 – ident: e_1_2_6_5_4 doi: 10.1016/j.tetasy.2010.06.011 – ident: e_1_2_6_28_1 doi: 10.1002/adsc.201700280 – ident: e_1_2_6_47_1 doi: 10.1039/C5CS00929D – ident: e_1_2_6_3_9 doi: 10.2533/chimia.2018.610 – ident: e_1_2_6_33_1 doi: 10.1002/9781118778173.ch13 – ident: e_1_2_6_50_5 doi: 10.1021/acscatal.6b02446 – ident: e_1_2_6_2_2 doi: 10.1002/ange.200901843 – ident: e_1_2_6_34_1 doi: 10.1002/adsc.200600294 – ident: e_1_2_6_5_3 doi: 10.1021/ja074824t – ident: e_1_2_6_8_2 doi: 10.1021/ja807243t – ident: e_1_2_6_46_1 doi: 10.1016/S0040-4039(00)96520-1 – ident: e_1_2_6_9_3 doi: 10.1021/ja005570d – ident: e_1_2_6_32_3 doi: 10.1002/jhet.5570160435 – ident: e_1_2_6_51_4 doi: 10.1002/anie.201404029 – ident: e_1_2_6_14_6 doi: 10.1002/ange.200906550 – ident: e_1_2_6_12_1 – ident: e_1_2_6_3_10 doi: 10.1007/128_2014_589 – ident: e_1_2_6_8_3 doi: 10.1021/ol202046y – ident: e_1_2_6_21_4 doi: 10.1039/C4CC04633A – ident: e_1_2_6_21_8 doi: 10.1002/cctc.201200224 – ident: e_1_2_6_3_1 doi: 10.1002/ejoc.201700120 – ident: e_1_2_6_40_1 doi: 10.1021/acs.joc.9b00143 – ident: e_1_2_6_51_1 doi: 10.1016/j.jorganchem.2019.06.032 – ident: e_1_2_6_5_2 doi: 10.1021/ja1095045 – volume: 5 start-page: 131 year: 2001 ident: e_1_2_6_37_1 publication-title: Targets Heterocycl. Syst – ident: e_1_2_6_45_2 doi: 10.1002/anie.201405381 – ident: e_1_2_6_27_1 doi: 10.1002/chem.201503598 – ident: e_1_2_6_3_5 doi: 10.1002/ijch.201300040 – ident: e_1_2_6_30_1 doi: 10.1039/C6QO00087H – ident: e_1_2_6_10_1 doi: 10.1039/c3cc41514g – ident: e_1_2_6_42_1 doi: 10.1039/C9QO00647H – ident: e_1_2_6_26_1 doi: 10.1039/C4CC08736D – ident: e_1_2_6_34_6 doi: 10.1021/acs.orglett.7b01868 – ident: e_1_2_6_3_13 doi: 10.1016/B978-0-08-095167-6.00222-6 – ident: e_1_2_6_18_2 doi: 10.1002/ange.200907078 – ident: e_1_2_6_14_3 doi: 10.1002/anie.200704566 – ident: e_1_2_6_41_1 doi: 10.1021/ja200084a – ident: e_1_2_6_48_2 doi: 10.1039/C6CC04474C – ident: e_1_2_6_17_1 doi: 10.1039/C3CC45518A – ident: e_1_2_6_34_5 doi: 10.1039/C1OB06604H – ident: e_1_2_6_25_1 doi: 10.1039/b907043e – ident: e_1_2_6_34_3 doi: 10.1039/c0cc03621h – start-page: 567 volume-title: Chemistry of Organogold Compounds year: 2014 ident: e_1_2_6_13_2 – ident: e_1_2_6_2_4 doi: 10.1002/ejoc.201800125 – ident: e_1_2_6_34_4 doi: 10.1002/chem.201100260 – ident: e_1_2_6_33_2 doi: 10.1016/B978-0-12-408100-0.00001-X – ident: e_1_2_6_5_1 doi: 10.1021/jo070579k – ident: e_1_2_6_8_4 doi: 10.1039/C6CC00633G – ident: e_1_2_6_14_2 doi: 10.1002/chem.200900164 – ident: e_1_2_6_39_1 doi: 10.1039/C4QO00130C – ident: e_1_2_6_37_2 doi: 10.1002/ejoc.201403580 – ident: e_1_2_6_4_3 doi: 10.1002/ejoc.201300725 – ident: e_1_2_6_21_6 doi: 10.1016/j.tetlet.2013.10.036 – ident: e_1_2_6_14_1 doi: 10.1021/ja901649s – ident: e_1_2_6_50_2 doi: 10.1002/cnma.201800132 – ident: e_1_2_6_35_2 doi: 10.1021/jacs.6b01008 – ident: e_1_2_6_32_1 doi: 10.1002/jhet.5570140605 – ident: e_1_2_6_21_7 doi: 10.1002/ijch.201300029 – ident: e_1_2_6_32_4 doi: 10.1016/j.tet.2007.07.068 – ident: e_1_2_6_21_3 doi: 10.1002/chem.201602822 – ident: e_1_2_6_3_2 doi: 10.1055/s-0035-1561638 – ident: e_1_2_6_7_1 doi: 10.1021/cr078346g – ident: e_1_2_6_21_11 doi: 10.1021/ar400188g – ident: e_1_2_6_51_5 doi: 10.1002/ange.201404029 – ident: e_1_2_6_9_2 doi: 10.1002/ange.200802517 – ident: e_1_2_6_3_12 doi: 10.1021/ar4001839 – ident: e_1_2_6_24_1 doi: 10.1021/ja062707c – ident: e_1_2_6_4_2 doi: 10.1055/s-0032-1317588 – ident: e_1_2_6_48_3 doi: 10.1007/s10562-014-1400-8 – ident: e_1_2_6_35_1 doi: 10.1002/ejoc.201500878 – ident: e_1_2_6_36_1 doi: 10.1002/adsc.201000644 – ident: e_1_2_6_22_1 doi: 10.1021/ja3065446 – ident: e_1_2_6_20_2 doi: 10.1021/cs400922y – ident: e_1_2_6_2_3 doi: 10.1039/C7OB00413C – ident: e_1_2_6_44_1 doi: 10.1021/jacs.7b07531 – ident: e_1_2_6_3_6 doi: 10.1351/PAC-CON-11-09-05 – ident: e_1_2_6_29_1 doi: 10.1039/C5SC01827G – ident: e_1_2_6_43_1 doi: 10.1002/chem.201402500 – ident: e_1_2_6_11_1 doi: 10.1055/s-2005-918509 – ident: e_1_2_6_18_1 doi: 10.1002/anie.200907078 – ident: e_1_2_6_13_4 – ident: e_1_2_6_45_1 doi: 10.1007/BF00506385 – ident: e_1_2_6_34_2 doi: 10.1039/c0cc03620j – ident: e_1_2_6_47_2 – ident: e_1_2_6_3_4 doi: 10.1246/cl.131230 – ident: e_1_2_6_13_3 doi: 10.1039/c3cs60441a – ident: e_1_2_6_19_1 doi: 10.1002/adsc.201500913 – ident: e_1_2_6_48_1 doi: 10.1021/acs.accounts.8b00625 – ident: e_1_2_6_31_2 doi: 10.1021/jm00161a026 – ident: e_1_2_6_50_1 doi: 10.1021/acs.accounts.9b00144 – ident: e_1_2_6_23_1 doi: 10.1039/c2cs15333e – ident: e_1_2_6_2_1 doi: 10.1002/anie.200901843 – ident: e_1_2_6_20_1 doi: 10.1002/9783527646869.ch4 – ident: e_1_2_6_33_3 doi: 10.1021/acs.orglett.9b02085 – ident: e_1_2_6_3_11 doi: 10.1021/ar4002558 – ident: e_1_2_6_21_10 doi: 10.1002/chem.201601129 – ident: e_1_2_6_51_2 doi: 10.1021/acs.orglett.6b00191 – ident: e_1_2_6_13_1 doi: 10.1021/acs.accounts.8b00567 – ident: e_1_2_6_14_5 doi: 10.1002/anie.200906550 – ident: e_1_2_6_15_1 doi: 10.1002/adsc.201000597 – ident: e_1_2_6_3_3 doi: 10.1515/pac-2016-0101 – ident: e_1_2_6_32_2 doi: 10.1002/jhet.5570150126 – volume: 771 start-page: 78 year: 2014 ident: e_1_2_6_21_5 publication-title: J. Organomet. Chem – ident: e_1_2_6_49_1 doi: 10.1002/cctc.201000413 – start-page: 1501 year: 2011 ident: e_1_2_6_21_9 publication-title: Synthesis – ident: e_1_2_6_6_1 doi: 10.3762/bjoc.7.124 – ident: e_1_2_6_9_1 doi: 10.1002/anie.200802517 – ident: e_1_2_6_45_3 doi: 10.1002/ange.201405381 – ident: e_1_2_6_51_6 doi: 10.1039/c2cc33030j – ident: e_1_2_6_16_1 doi: 10.1039/c0sc00630k – ident: e_1_2_6_50_4 doi: 10.1002/chem.201700727 – ident: e_1_2_6_46_2 doi: 10.1002/jlac.199019900185 – ident: e_1_2_6_3_8 doi: 10.1002/ange.201107575 – ident: e_1_2_6_21_1 doi: 10.1002/anie.201710105 – ident: e_1_2_6_14_4 doi: 10.1002/ange.200704566 |
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| Snippet | The reactivity of vinyl‐/furoindole derivatives with gold‐activated π‐systems is the subject of extensive investigation. In the presence of these electrophilic... |
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| SubjectTerms | Allenes Carbene ligands Cascade chemical reactions Chemical reactions Cycloaddition Derivatives Gold Homogeneous catalysis Indoles Inorganic chemistry |
| Title | Vinyl‐/Furoindoles and Gold Catalysis: New Achievements and Future Perspectives for the Synthesis of Complex Indole Derivatives |
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