Enabling syntheses of diterpenoid alkaloids and related diterpenes by an oxidative dearomatization/Diels-Alder cycloaddition strategy
Covering: 2015 to March 2017 ortho -Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels-Alder cycloadditions, facilitating rapid access to molecular com...
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Published in | Natural product reports Vol. 34; no. 9; pp. 144 - 15 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
30.08.2017
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Subjects | |
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Abstract | Covering: 2015 to March 2017
ortho
-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels-Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight.
Recent accomplishments in the total syntheses of diterpenoid alkaloids and their biosynthetically associated diterpenes have highly relied on an oxidative dearomatization/Diels-Alder cycloaddition strategy, and are highlighted in this article. |
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AbstractList | Covering: 2015 to March 2017ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels-Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight. Covering: 2015 to March 2017ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels-Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight.Covering: 2015 to March 2017ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels-Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight. Covering: 2015 to March 2017 ortho -Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels-Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight. Recent accomplishments in the total syntheses of diterpenoid alkaloids and their biosynthetically associated diterpenes have highly relied on an oxidative dearomatization/Diels-Alder cycloaddition strategy, and are highlighted in this article. Covering: 2015 to March 2017 ortho -Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels–Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight. Covering: 2015 to March 2017 ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis. One of their most important applications involves the participation in Diels–Alder cycloadditions, facilitating rapid access to molecular complexity. This powerful strategy has recently been utilized in the syntheses of diverse diterpenoid alkaloids and their biogenetically relevant diterpenes, which is the subject of this Highlight. |
Author | Liu, Xiao-Yu Qin, Yong |
AuthorAffiliation | Key Laboratory of Drug Targeting and Drug Delivery Systems of the Ministry of Education Sichuan University West China School of Pharmacy |
AuthorAffiliation_xml | – name: West China School of Pharmacy – name: Sichuan University – name: Key Laboratory of Drug Targeting and Drug Delivery Systems of the Ministry of Education |
Author_xml | – sequence: 1 givenname: Xiao-Yu surname: Liu fullname: Liu, Xiao-Yu – sequence: 2 givenname: Yong surname: Qin fullname: Qin, Yong |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28799605$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1002/anie.201609882 10.1021/ja8078835 10.1038/nature16440 10.1007/BF02234909 10.1002/anie.201508996 10.1002/anie.200460332 10.1021/ja503023h 10.1021/ja4064958 10.1002/anie.201103950 10.1021/jacs.5b08958 10.1139/v78-237 10.1021/jo961529a 10.1021/ja01056a043 10.1002/anie.201305822 10.1016/j.tetlet.2008.11.028 10.1002/anie.201006017 10.1016/S0040-4039(01)82712-X 10.1002/ijch.201100005 10.1021/acs.joc.6b01011 10.1038/ncomms12183 10.1039/C6OB00053C 10.1021/ja507321j 10.1021/cr0306900 10.1016/j.tet.2009.12.046 10.1021/ja00159a042 10.1021/ja00822a048 10.1021/acs.orglett.6b00789 10.1016/j.tet.2015.11.050 10.1016/j.tet.2016.04.027 10.1016/S1099-4831(09)06701-7 10.1039/c3ob42541j 10.1039/b916679c 10.1021/ar000194n 10.1002/jlac.19596280112 10.1055/s-0034-1379906 10.1002/ajoc.201500295 10.1351/pac197951040689 10.1039/C6SC00671J 10.1021/jacs.6b07268 10.1016/j.cclet.2016.11.010 10.2174/0929867033456684 10.1021/ja0625430 10.1002/anie.201209030 10.1039/C1OB06704D 10.1002/anie.200800167 10.1023/A:1014479628541 10.1021/ja00898a048 10.1016/j.tetlet.2016.02.110 10.1002/9780470742761 10.1016/j.tet.2015.11.057 10.1139/v80-298 |
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Notes | Yong Qin received his BS degree from Yunnan University in 1989 and his PhD from the Institute of Chemistry, Chinese Academy of Sciences in 1995. After a short stay at the Chengdu Institute of Organic Chemistry as an assistant and associate professor, he moved to the USA, working as a postdoctoral associate (1996 to 2000) at the University of Vermont. He was a research scientist at Triad Therapeutics (San Diego) before he joined the faculty of Sichuan University as a full professor in 2003. His research has been focused on the total synthesis of bioactive natural products and medicinal chemistry. Xiao-Yu Liu was born in 1985 in Sichuan Province, China. He received his PhD degree in 2012 under the supervision of Prof. Feng-Peng Wang at Sichuan University. He then carried out postdoctoral studies at Seoul National University with Prof. David Y.-K. Chen. After that, he joined the faculty of Sichuan University in 2014 working with Prof. Yong Qin. His research interests include target- and diversity-oriented synthesis based on complex natural products, especially the diterpenoid alkaloids. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
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References | Peese (C7NP00033B-(cit4f)/*[position()=1]) 2006; 128 Schneider (C7NP00033B-(cit23b)/*[position()=1]) 1959; 628 Tang (C7NP00033B-(cit19a)/*[position()=1]) 2009; 50 Fujioka (C7NP00033B-(cit13d)/*[position()=1]) 2016; 27 Suzuki (C7NP00033B-(cit4g)/*[position()=1]) 2011; 50 Cherney (C7NP00033B-(cit4k)/*[position()=1]) 2014; 136 Wang (C7NP00033B-(cit1d)/*[position()=1]) 2010; vol. 69 Pouységu (C7NP00033B-(cit14c)/*[position()=1]) 2010; 66 Wiesner (C7NP00033B-(cit23a)/*[position()=1]) 1959; 1 Han (C7NP00033B-(cit22)/*[position()=1]) 1996; 61 Zhu (C7NP00033B-(cit5d)/*[position()=1]) 2015; 47 Tashkhodzhaev (C7NP00033B-(cit19b)/*[position()=1]) 2000; 36 Wang (C7NP00033B-(cit1c)/*[position()=1]) 2009; vol. 67 Wang (C7NP00033B-(cit1a)/*[position()=1]) 2010; 27 Hamlin (C7NP00033B-(cit5b)/*[position()=1]) 2014; 12 Wiesner (C7NP00033B-(cit15a)/*[position()=1]) 1978; 56 Hao (C7NP00033B-(cit18)/*[position()=1]) 2003; 10 Nagata (C7NP00033B-(cit4a)/*[position()=1]) 1963; 85 Hamlin (C7NP00033B-(cit4i)/*[position()=1]) 2013; 52 Song (C7NP00033B-(cit7)/*[position()=1]) 2015; 137 Masamune (C7NP00033B-(cit4b)/*[position()=1]) 1964; 86 Nishiyama (C7NP00033B-(cit9)/*[position()=1]) 2016; 18 Tang (C7NP00033B-(cit13c)/*[position()=1]) 2016; 14 Trost (C7NP00033B-(cit17)/*[position()=1]) 2008; 130 Cheng (C7NP00033B-(cit8)/*[position()=1]) 2016; 55 Gong (C7NP00033B-(cit11)/*[position()=1]) 2016; 7 Liu (C7NP00033B-(cit20)/*[position()=1]) 2012; 10 Dewick (C7NP00033B-(cit2)/*[position()=1]) 2009 Kou (C7NP00033B-(cit10)/*[position()=1]) 2016; 138 Roche (C7NP00033B-(cit14d)/*[position()=1]) 2011; 50 Muratake (C7NP00033B-(cit4e)/*[position()=1]) 2004; 43 Breitler (C7NP00033B-(cit4j)/*[position()=1]) 2013; 52 Magdziak (C7NP00033B-(cit14b)/*[position()=1]) 2004; 104 Meng (C7NP00033B-(cit19d)/*[position()=1]) 2017; 28 Ihara (C7NP00033B-(cit4d)/*[position()=1]) 1990; 112 Liu (C7NP00033B-(cit5c)/*[position()=1]) 2015; 4 Hagiwara (C7NP00033B-(cit13a)/*[position()=1]) 2016; 7 Dickson (C7NP00033B-(cit13f)/*[position()=1]) 2016; 72 Maimone (C7NP00033B-(cit21)/*[position()=2]) 2008; 47 Tabuchi (C7NP00033B-(cit13b)/*[position()=1]) 2016; 81 Li (C7NP00033B-(cit13g)/*[position()=1]) 2016; 72 Shi (C7NP00033B-(cit4h)/*[position()=1]) 2013; 135 Nishiyama (C7NP00033B-(cit4l)/*[position()=1]) 2014; 136 Wang (C7NP00033B-(cit1b)/*[position()=1]) 2002; vol. 59 Jiang (C7NP00033B-(cit13h)/*[position()=1]) 2016; 57 Li (C7NP00033B-(cit12)/*[position()=1]) 2016; 55 Wiesner (C7NP00033B-(cit15b)/*[position()=1]) 1979; 51 Saidkhodzhaeva (C7NP00033B-(cit19c)/*[position()=1]) 2001; 37 Wiesner (C7NP00033B-(cit4c)/*[position()=1]) 1974; 96 Marth (C7NP00033B-(cit6)/*[position()=1]) 2015; 528 Cherney (C7NP00033B-(cit5a)/*[position()=1]) 2011; 51 Chen (C7NP00033B-(cit13e)/*[position()=1]) 2016; 72 Wada (C7NP00033B-(cit3)/*[position()=1]) 2012; vol. 38 Sethi (C7NP00033B-(cit16)/*[position()=2]) 1980; 58 Liao (C7NP00033B-(cit14a)/*[position()=1]) 2002; 35 |
References_xml | – issn: 2009 publication-title: Medicinal Natural Products: A Biosynthetic Approach doi: Dewick – issn: 2012 issue: vol. 38 end-page: 191 publication-title: Studies in Natural Products Chemistry doi: Wada – issn: 2010 issue: vol. 69 end-page: 1 publication-title: The Alkaloids: Chemistry and Biology doi: Wang Chen – issn: 2009 issue: vol. 67 end-page: 1 publication-title: The Alkaloids: Chemistry and Biology doi: Wang Chen Liang – issn: 2002 issue: vol. 59 end-page: 1 publication-title: The Alkaloids: Chemistry and Biology doi: Wang Liang – volume: 55 start-page: 15667 year: 2016 ident: C7NP00033B-(cit12)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201609882 – volume: 130 start-page: 16176 year: 2008 ident: C7NP00033B-(cit17)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja8078835 – volume: 528 start-page: 493 year: 2015 ident: C7NP00033B-(cit6)/*[position()=1] publication-title: Nature doi: 10.1038/nature16440 – volume: 36 start-page: 79 year: 2000 ident: C7NP00033B-(cit19b)/*[position()=1] publication-title: Chem. Nat. Compd. doi: 10.1007/BF02234909 – volume: 55 start-page: 392 year: 2016 ident: C7NP00033B-(cit8)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201508996 – volume: 43 start-page: 4646 year: 2004 ident: C7NP00033B-(cit4e)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200460332 – volume: 136 start-page: 6598 year: 2014 ident: C7NP00033B-(cit4l)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja503023h – volume: 135 start-page: 14313 year: 2013 ident: C7NP00033B-(cit4h)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja4064958 – volume: 50 start-page: 9177 year: 2011 ident: C7NP00033B-(cit4g)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201103950 – volume: 137 start-page: 13706 year: 2015 ident: C7NP00033B-(cit7)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.5b08958 – volume: 56 start-page: 1451 year: 1978 ident: C7NP00033B-(cit15a)/*[position()=1] publication-title: Can. J. Chem. doi: 10.1139/v78-237 – volume: 61 start-page: 9483 year: 1996 ident: C7NP00033B-(cit22)/*[position()=1] publication-title: J. Org. Chem. doi: 10.1021/jo961529a – volume: 86 start-page: 291 year: 1964 ident: C7NP00033B-(cit4b)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja01056a043 – volume: 52 start-page: 11168 year: 2013 ident: C7NP00033B-(cit4j)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201305822 – volume: 50 start-page: 460 year: 2009 ident: C7NP00033B-(cit19a)/*[position()=1] publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2008.11.028 – volume: 50 start-page: 4068 year: 2011 ident: C7NP00033B-(cit14d)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201006017 – volume: vol. 59 start-page: 1 volume-title: The Alkaloids: Chemistry and Biology year: 2002 ident: C7NP00033B-(cit1b)/*[position()=1] – volume: 1 start-page: 15 year: 1959 ident: C7NP00033B-(cit23a)/*[position()=1] publication-title: Tetrahedron Lett. doi: 10.1016/S0040-4039(01)82712-X – volume: 51 start-page: 391 year: 2011 ident: C7NP00033B-(cit5a)/*[position()=1] publication-title: Isr. J. Chem. doi: 10.1002/ijch.201100005 – volume: 81 start-page: 10204 year: 2016 ident: C7NP00033B-(cit13b)/*[position()=1] publication-title: J. Org. Chem. doi: 10.1021/acs.joc.6b01011 – volume: 7 start-page: 12183 year: 2016 ident: C7NP00033B-(cit11)/*[position()=1] publication-title: Nat. Commun. doi: 10.1038/ncomms12183 – volume: 14 start-page: 2716 year: 2016 ident: C7NP00033B-(cit13c)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/C6OB00053C – volume: 136 start-page: 12592 year: 2014 ident: C7NP00033B-(cit4k)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja507321j – volume: 104 start-page: 1383 year: 2004 ident: C7NP00033B-(cit14b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr0306900 – volume: vol. 69 start-page: 1 volume-title: The Alkaloids: Chemistry and Biology year: 2010 ident: C7NP00033B-(cit1d)/*[position()=1] – volume: 66 start-page: 2235 year: 2010 ident: C7NP00033B-(cit14c)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2009.12.046 – volume: 112 start-page: 1164 year: 1990 ident: C7NP00033B-(cit4d)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00159a042 – volume: 96 start-page: 4990 year: 1974 ident: C7NP00033B-(cit4c)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00822a048 – volume: 18 start-page: 2359 year: 2016 ident: C7NP00033B-(cit9)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.6b00789 – volume: 72 start-page: 347 year: 2016 ident: C7NP00033B-(cit13e)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2015.11.050 – volume: 72 start-page: 3171 year: 2016 ident: C7NP00033B-(cit13g)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2016.04.027 – volume: vol. 67 start-page: 1 volume-title: The Alkaloids: Chemistry and Biology year: 2009 ident: C7NP00033B-(cit1c)/*[position()=1] doi: 10.1016/S1099-4831(09)06701-7 – volume: 12 start-page: 1846 year: 2014 ident: C7NP00033B-(cit5b)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/c3ob42541j – volume: 27 start-page: 529 year: 2010 ident: C7NP00033B-(cit1a)/*[position()=1] publication-title: Nat. Prod. Rep. doi: 10.1039/b916679c – volume: 35 start-page: 856 year: 2002 ident: C7NP00033B-(cit14a)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar000194n – volume: 628 start-page: 114 year: 1959 ident: C7NP00033B-(cit23b)/*[position()=1] publication-title: Justus Liebigs Ann. Chem. doi: 10.1002/jlac.19596280112 – volume: 47 start-page: 2691 year: 2015 ident: C7NP00033B-(cit5d)/*[position()=1] publication-title: Synthesis doi: 10.1055/s-0034-1379906 – volume: 4 start-page: 1010 year: 2015 ident: C7NP00033B-(cit5c)/*[position()=1] publication-title: Asian J. Org. Chem. doi: 10.1002/ajoc.201500295 – volume: 51 start-page: 689 year: 1979 ident: C7NP00033B-(cit15b)/*[position()=1] publication-title: Pure Appl. Chem. doi: 10.1351/pac197951040689 – volume: 7 start-page: 4372 year: 2016 ident: C7NP00033B-(cit13a)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/C6SC00671J – volume: 138 start-page: 10830 year: 2016 ident: C7NP00033B-(cit10)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.6b07268 – volume: 28 start-page: 588 year: 2017 ident: C7NP00033B-(cit19d)/*[position()=1] publication-title: Chin. Chem. Lett. doi: 10.1016/j.cclet.2016.11.010 – volume: 10 start-page: 2253 year: 2003 ident: C7NP00033B-(cit18)/*[position()=1] publication-title: Curr. Med. Chem. doi: 10.2174/0929867033456684 – volume: 128 start-page: 8734 year: 2006 ident: C7NP00033B-(cit4f)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0625430 – volume: 52 start-page: 4854 year: 2013 ident: C7NP00033B-(cit4i)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201209030 – volume: 10 start-page: 1411 year: 2012 ident: C7NP00033B-(cit20)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/C1OB06704D – volume: 47 start-page: 3054 year: 2008 ident: C7NP00033B-(cit21)/*[position()=2] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200800167 – volume: vol. 38 start-page: 191 volume-title: Studies in Natural Products Chemistry year: 2012 ident: C7NP00033B-(cit3)/*[position()=1] – volume: 37 start-page: 466 year: 2001 ident: C7NP00033B-(cit19c)/*[position()=1] publication-title: Chem. Nat. Compd. doi: 10.1023/A:1014479628541 – volume: 85 start-page: 2342 year: 1963 ident: C7NP00033B-(cit4a)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00898a048 – volume: 57 start-page: 1610 year: 2016 ident: C7NP00033B-(cit13h)/*[position()=1] publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2016.02.110 – volume: 27 start-page: 621 year: 2016 ident: C7NP00033B-(cit13d)/*[position()=1] publication-title: Synlett – volume-title: Medicinal Natural Products: A Biosynthetic Approach year: 2009 ident: C7NP00033B-(cit2)/*[position()=1] doi: 10.1002/9780470742761 – volume: 72 start-page: 400 year: 2016 ident: C7NP00033B-(cit13f)/*[position()=1] publication-title: Tetrahedron doi: 10.1016/j.tet.2015.11.057 – volume: 58 start-page: 1889 year: 1980 ident: C7NP00033B-(cit16)/*[position()=2] publication-title: Can. J. Chem. doi: 10.1139/v80-298 |
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ortho
-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis.... Covering: 2015 to March 2017ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis.... Covering: 2015 to March 2017 ortho-Benzoquinones generated from dearomatization of aromatic compounds are highly reactive intermediates in organic synthesis.... |
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SubjectTerms | Alkaloids - chemical synthesis Alkaloids - chemistry benzoquinones Cycloaddition Reaction cycloaddition reactions Diterpenes - chemical synthesis Diterpenes - chemistry diterpenoid alkaloids Molecular Structure Oxidation-Reduction Stereoisomerism |
Title | Enabling syntheses of diterpenoid alkaloids and related diterpenes by an oxidative dearomatization/Diels-Alder cycloaddition strategy |
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