Visible‐Light‐Promoted Cascade Radical Cyclization: Synthesis of 1,4‐Diketones Containing Chroman‐4‐One Skeletons
A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes advantages of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4‐diketones bearing bio...
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Published in | Chemistry, an Asian journal Vol. 14; no. 19; pp. 3269 - 3273 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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01.10.2019
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Abstract | A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes advantages of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4‐diketones bearing biologically important chroman‐4‐one skeletons with moderate to good yields.
A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes advantage of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4‐diketones bearing biologically important chroman‐4‐one skeletons in moderate to good yields. |
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AbstractList | A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes advantages of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4‐diketones bearing biologically important chroman‐4‐one skeletons with moderate to good yields. A visible-light-induced cascade radical cyclization of aroyl chlorides with 2-(allyloxy)-benzaldehyde derivatives has been developed. The method takes advantages of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4-diketones bearing biologically important chroman-4-one skeletons with moderate to good yields.A visible-light-induced cascade radical cyclization of aroyl chlorides with 2-(allyloxy)-benzaldehyde derivatives has been developed. The method takes advantages of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4-diketones bearing biologically important chroman-4-one skeletons with moderate to good yields. A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes advantages of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4‐diketones bearing biologically important chroman‐4‐one skeletons with moderate to good yields. A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes advantage of unactivated C=C bonds as the acyl radical acceptors and offers a mild and green approach for the synthesis of 1,4‐diketones bearing biologically important chroman‐4‐one skeletons in moderate to good yields. |
Author | Wang, Long He, Xiang‐Kui Xuan, Jun Cai, Bao‐Gui Yang, Qing‐Qing |
Author_xml | – sequence: 1 givenname: Xiang‐Kui surname: He fullname: He, Xiang‐Kui organization: Anhui University – sequence: 2 givenname: Bao‐Gui surname: Cai fullname: Cai, Bao‐Gui organization: Anhui University – sequence: 3 givenname: Qing‐Qing surname: Yang fullname: Yang, Qing‐Qing organization: China Three Gorges University – sequence: 4 givenname: Long surname: Wang fullname: Wang, Long email: wanglongchem@ctgu.edu.cn organization: China Three Gorges University – sequence: 5 givenname: Jun orcidid: 0000-0003-0578-9330 surname: Xuan fullname: Xuan, Jun email: xuanjun@ahu.edu.cn organization: Ministry of Education |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31464012$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1002/chem.201304823 10.1002/anie.200604820 10.6023/cjoc201806009 10.1007/s11426-018-9399-2 10.1055/s-1993-22381 10.1039/C6CS00912C 10.1016/j.tet.2018.12.023 10.1002/ange.201004854 10.1039/B913880N 10.1055/s-0037-1610329 10.1016/S0040-4039(01)81920-1 10.1002/anie.201809601 10.1002/ange.200604820 10.1002/anie.201810798 10.1021/ol2023483 10.1021/acs.orglett.9b01338 10.1039/C5CC09730D 10.1016/S0065-2725(08)60594-2 10.1002/adsc.201601407 10.1039/b104000f 10.1002/adsc.201700913 10.1002/asia.201701738 10.1002/anie.201004854 10.1021/acs.orglett.5b02392 10.1002/ajoc.201900272 10.1021/acs.jmedchem.6b01117 10.1021/cr60225a004 10.1021/ol034252r 10.1002/chem.201704224 10.1039/p29760001047 10.1002/adsc.201801181 10.1002/adsc.201701072 10.1002/anie.199610501 10.1021/acs.orglett.8b03840 10.1016/j.jorganchem.2004.04.045 10.1002/ange.201810798 10.1002/anie.201200223 10.1002/asia.201801496 10.1002/ange.19760882103 10.1002/anie.201709766 10.1039/b210764c 10.1039/c3ob40137e 10.1002/cjoc.201600729 10.1021/ja204226n 10.1021/acs.orglett.7b03794 10.1039/b602596j 10.1002/cber.188401702228 10.1002/chem.201304898 10.7164/antibiotics.49.50 10.1016/j.scib.2019.02.002 10.1021/jo00269a001 10.1002/352760183X 10.1021/jm500930h 10.1002/anie.197606391 10.1002/ange.201200223 10.1021/cr300503r 10.1021/acs.orglett.8b02627 10.1021/acs.chemrev.6b00057 10.1039/C7QO00453B 10.1002/ange.19961081005 10.1021/acs.orglett.9b01416 10.1039/C9CC01047E 10.1021/jo00083a029 10.1002/ange.201709766 10.1016/j.tet.2006.05.024 10.1002/cber.188401702254 10.1021/ja00362a047 10.1002/ange.201809601 10.1039/C8GC03810D 10.1021/acs.orglett.6b03684 10.1021/acs.orglett.7b01162 10.1016/j.tetlet.2008.10.139 |
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Keywords | Photoredox catalysis Radical cyclization Visible light Acyl radical 1,4-Diketones |
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References | 2019; 51 2017; 4 2019; 55 2017; 46 1976 2011; 13 2019; 361 2004; 689 1993; 1993 2017; 359 2014; 20 1983; 105 2019; 62 2019 2019 2006; 62 2013; 11 2019; 64 2009; 50 2019; 21 2012 2012; 51 124 2018 2018; 57 130 2017; 35 2003; 5 2013; 113 2014; 57 2016; 116 2018; 38 2019; 8 2015; 17 2019; 75 1963; 63 2011; 40 2017; 23 2016; 52 2006; 4 2003 1976 1976; 15 88 2018; 20 2016; 59 2011; 133 2019 2019; 58 131 1981; 22 1967; 7 1996 1996; 35 108 1989; 54 2007 2007; 46 119 1884; 17 2017; 19 1994; 59 2011 2011; 50 123 2013 1996; 49 2001; 30 2018; 13 e_1_2_2_24_2 e_1_2_2_47_2 e_1_2_2_4_2 e_1_2_2_22_3 e_1_2_2_22_2 e_1_2_2_49_2 e_1_2_2_6_2 e_1_2_2_20_3 e_1_2_2_20_2 e_1_2_2_2_2 e_1_2_2_62_2 e_1_2_2_41_1 e_1_2_2_64_2 e_1_2_2_8_2 e_1_2_2_28_2 e_1_2_2_43_2 e_1_2_2_26_3 e_1_2_2_66_1 e_1_2_2_26_2 e_1_2_2_45_2 e_1_2_2_68_2 e_1_2_2_8_3 e_1_2_2_60_2 e_1_2_2_13_2 e_1_2_2_36_2 e_1_2_2_38_1 e_1_2_2_57_3 e_1_2_2_59_1 e_1_2_2_11_2 (e_1_2_2_42_2) 2013 e_1_2_2_74_2 e_1_2_2_51_1 e_1_2_2_72_2 e_1_2_2_76_1 e_1_2_2_19_2 e_1_2_2_30_2 e_1_2_2_53_1 e_1_2_2_17_2 e_1_2_2_32_2 e_1_2_2_78_2 e_1_2_2_55_1 e_1_2_2_34_2 e_1_2_2_15_1 e_1_2_2_34_3 e_1_2_2_70_2 Zhang K. (e_1_2_2_57_2) 2019 e_1_2_2_3_2 e_1_2_2_5_1 e_1_2_2_23_2 e_1_2_2_48_2 e_1_2_2_69_2 e_1_2_2_21_1 e_1_2_2_1_1 e_1_2_2_40_2 e_1_2_2_61_2 e_1_2_2_29_3 e_1_2_2_29_2 e_1_2_2_63_2 e_1_2_2_7_2 e_1_2_2_44_2 e_1_2_2_65_2 e_1_2_2_27_1 e_1_2_2_46_1 e_1_2_2_9_2 e_1_2_2_25_2 e_1_2_2_67_2 e_1_2_2_12_2 e_1_2_2_37_2 e_1_2_2_10_2 e_1_2_2_39_2 e_1_2_2_50_3 e_1_2_2_52_1 e_1_2_2_50_2 e_1_2_2_75_2 e_1_2_2_54_1 e_1_2_2_73_1 e_1_2_2_18_2 e_1_2_2_31_2 e_1_2_2_16_2 e_1_2_2_33_2 e_1_2_2_79_2 e_1_2_2_56_3 e_1_2_2_58_1 e_1_2_2_77_1 e_1_2_2_14_2 e_1_2_2_35_2 e_1_2_2_56_2 e_1_2_2_71_2 |
References_xml | – volume: 8 start-page: 1376 year: 2019 end-page: 1379 publication-title: Asian J. Org. Chem. – volume: 133 start-page: 10756 year: 2011 end-page: 10759 publication-title: J. Am. Chem. Soc. – volume: 50 123 start-page: 1869 1909 year: 2011 2011 end-page: 1872 1912 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 30 start-page: 313 year: 2001 end-page: 320 publication-title: Chem. Soc. Rev. – volume: 62 start-page: 24 year: 2019 end-page: 57 publication-title: Sci. China Chem. – volume: 20 start-page: 3045 year: 2014 end-page: 3049 publication-title: Chem. Eur. J. – volume: 17 start-page: 2756 year: 1884 publication-title: Ber. Dtsch. Chem. Ges. – year: 2019 2019 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 35 start-page: 311 year: 2017 end-page: 315 publication-title: Chin. J. Chem. – volume: 116 start-page: 10075 year: 2016 end-page: 10166 publication-title: Chem. Rev. – volume: 46 start-page: 4329 year: 2017 end-page: 4346 publication-title: Chem. Soc. Rev. – volume: 689 start-page: 3873 year: 2004 end-page: 3890 publication-title: J. Organomet. Chem. – volume: 359 start-page: 2390 year: 2017 end-page: 2395 publication-title: Adv. Synth. Catal. – volume: 63 start-page: 511 year: 1963 end-page: 556 publication-title: Chem. Rev. – volume: 54 start-page: 1777 year: 1989 end-page: 1779 publication-title: J. Org. Chem. – volume: 51 124 start-page: 6828 6934 year: 2012 2012 end-page: 6838 6944 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 75 start-page: 1647 year: 2019 end-page: 1651 publication-title: Tetrahedron – volume: 51 start-page: 303 year: 2019 end-page: 333 publication-title: Synthesis – volume: 15 88 start-page: 639 695 year: 1976 1976 end-page: 647 704 publication-title: Angew. Chem. Int. Ed. Engl. Angew. Chem. – volume: 4 start-page: 2230 year: 2017 end-page: 2234 publication-title: Org. Chem. Front. – volume: 359 start-page: 3560 year: 2017 end-page: 3565 publication-title: Adv. Synth. Catal. – volume: 7 start-page: 377 year: 1967 end-page: 490 publication-title: Adv. Heterocycl. Chem. – volume: 38 start-page: 3155 year: 2018 end-page: 3164 publication-title: Chin. J. Org. Chem. – volume: 46 119 start-page: 2531 2583 year: 2007 2007 end-page: 2534 2586 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 13 start-page: 5624 year: 2011 end-page: 5627 publication-title: Org. Lett. – volume: 20 start-page: 449 year: 2018 end-page: 452 publication-title: Org. Lett. – volume: 13 start-page: 3855 year: 2018 end-page: 3858 publication-title: Chem. Asian J. – volume: 58 131 start-page: 1208 1221 year: 2019 2019 end-page: 1212 1225 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 23 start-page: 15899 year: 2017 end-page: 15902 publication-title: Chem. Eur. J. – volume: 59 start-page: 10794 year: 2016 end-page: 10799 publication-title: J. Med. Chem. – volume: 57 start-page: 9870 year: 2014 end-page: 9888 publication-title: J. Med. Chem. – volume: 359 start-page: 3945 year: 2017 end-page: 3949 publication-title: Adv. Synth. Catal. – start-page: 1047 year: 1976 publication-title: J. Chem. Soc. Perkin Trans. 2 – volume: 19 start-page: 512 year: 2017 publication-title: Org. Lett. – volume: 21 start-page: 4153 year: 2019 end-page: 4158 publication-title: Org. Lett. – volume: 49 start-page: 50 year: 1996 end-page: 53 publication-title: J. Antibiot. – volume: 113 start-page: 5322 year: 2013 end-page: 5363 publication-title: Chem. Rev. – year: 2003 – volume: 105 start-page: 7200 year: 1983 end-page: 7202 publication-title: J. Am. Chem. Soc. – volume: 19 start-page: 2929 year: 2017 end-page: 2932 publication-title: Org. Lett. – volume: 55 start-page: 5408 year: 2019 end-page: 5419 publication-title: Chem. Commun. – volume: 50 start-page: 274 year: 2009 end-page: 276 publication-title: Tetrahedron Lett. – volume: 20 start-page: 6157 year: 2018 end-page: 6160 publication-title: Org. Lett. – volume: 40 start-page: 102 year: 2011 end-page: 113 publication-title: Chem. Soc. Rev. – volume: 22 start-page: 3417 year: 1981 end-page: 3420 publication-title: Tetrahedron Lett. – volume: 361 start-page: 1230 year: 2019 end-page: 1235 publication-title: Adv. Synth. Catal. – volume: 59 start-page: 850 year: 1994 end-page: 853 publication-title: J. Org. Chem. – volume: 35 108 start-page: 1050 1140 year: 1996 1996 end-page: 1066 1157 publication-title: Angew. Chem. Int. Ed. Engl. Angew. Chem. – volume: 62 start-page: 7213 year: 2006 end-page: 7256 publication-title: Tetrahedron – volume: 21 start-page: 748 year: 2019 end-page: 764 publication-title: Green Chem. – volume: 64 start-page: 337 year: 2019 end-page: 350 publication-title: Sci. Bull. – volume: 4 start-page: 2076 year: 2006 end-page: 2080 publication-title: Org. Biomol. Chem. – volume: 57 130 start-page: 10034 10188 year: 2018 2018 end-page: 10072 10228 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 58 131 start-page: 1213 1226 year: 2019 2019 end-page: 1217 1230 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 1993 start-page: 143 year: 1993 end-page: 145 publication-title: Synlett – volume: 11 start-page: 2387 year: 2013 end-page: 2403 publication-title: Org. Biomol. Chem. – volume: 17 start-page: 4830 year: 2015 end-page: 4833 publication-title: Org. Lett. – volume: 21 start-page: 913 year: 2019 end-page: 916 publication-title: Org. Lett. – volume: 13 start-page: 271 year: 2018 end-page: 274 publication-title: Chem. Asian J. – start-page: 204 year: 2003 end-page: 205 publication-title: Chem. Commun. – volume: 5 start-page: 1313 year: 2003 end-page: 1316 publication-title: Org. Lett. – volume: 17 start-page: 2863 year: 1884 end-page: 2870 publication-title: Ber. Dtsch. Chem. Ges. – volume: 52 start-page: 3661 year: 2016 end-page: 3664 publication-title: Chem. Commun. – volume: 20 start-page: 3874 year: 2014 end-page: 3886 publication-title: Chem. Eur. J. – year: 2013 – volume: 21 start-page: 4234 year: 2019 end-page: 4238 publication-title: Org. Lett. – ident: e_1_2_2_32_2 doi: 10.1002/chem.201304823 – ident: e_1_2_2_46_1 – ident: e_1_2_2_20_2 doi: 10.1002/anie.200604820 – ident: e_1_2_2_43_2 doi: 10.6023/cjoc201806009 – ident: e_1_2_2_36_2 doi: 10.1007/s11426-018-9399-2 – ident: e_1_2_2_18_2 doi: 10.1055/s-1993-22381 – ident: e_1_2_2_57_3 – ident: e_1_2_2_77_1 – ident: e_1_2_2_60_2 doi: 10.1039/C6CS00912C – ident: e_1_2_2_40_2 doi: 10.1016/j.tet.2018.12.023 – ident: e_1_2_2_38_1 – ident: e_1_2_2_26_3 doi: 10.1002/ange.201004854 – ident: e_1_2_2_28_2 doi: 10.1039/B913880N – volume-title: Photochemically-generated intermediates in synthesis year: 2013 ident: e_1_2_2_42_2 – ident: e_1_2_2_45_2 doi: 10.1055/s-0037-1610329 – ident: e_1_2_2_10_2 doi: 10.1016/S0040-4039(01)81920-1 – ident: e_1_2_2_15_1 – ident: e_1_2_2_50_2 doi: 10.1002/anie.201809601 – ident: e_1_2_2_20_3 doi: 10.1002/ange.200604820 – ident: e_1_2_2_56_2 doi: 10.1002/anie.201810798 – ident: e_1_2_2_74_2 doi: 10.1021/ol2023483 – ident: e_1_2_2_58_1 doi: 10.1021/acs.orglett.9b01338 – ident: e_1_2_2_69_2 doi: 10.1039/C5CC09730D – ident: e_1_2_2_6_2 doi: 10.1016/S0065-2725(08)60594-2 – ident: e_1_2_2_70_2 doi: 10.1002/adsc.201601407 – ident: e_1_2_2_11_2 doi: 10.1039/b104000f – ident: e_1_2_2_53_1 doi: 10.1002/adsc.201700913 – ident: e_1_2_2_54_1 doi: 10.1002/asia.201701738 – ident: e_1_2_2_26_2 doi: 10.1002/anie.201004854 – ident: e_1_2_2_55_1 – ident: e_1_2_2_41_1 – ident: e_1_2_2_47_2 doi: 10.1021/acs.orglett.5b02392 – year: 2019 ident: e_1_2_2_57_2 publication-title: Angew. Chem. Int. Ed. – ident: e_1_2_2_65_2 doi: 10.1002/ajoc.201900272 – ident: e_1_2_2_68_2 doi: 10.1021/acs.jmedchem.6b01117 – ident: e_1_2_2_7_2 doi: 10.1021/cr60225a004 – ident: e_1_2_2_24_2 doi: 10.1021/ol034252r – ident: e_1_2_2_52_1 doi: 10.1002/chem.201704224 – ident: e_1_2_2_66_1 – ident: e_1_2_2_78_2 doi: 10.1039/p29760001047 – ident: e_1_2_2_64_2 doi: 10.1002/adsc.201801181 – ident: e_1_2_2_71_2 doi: 10.1002/adsc.201701072 – ident: e_1_2_2_22_2 doi: 10.1002/anie.199610501 – ident: e_1_2_2_49_2 doi: 10.1021/acs.orglett.8b03840 – ident: e_1_2_2_12_2 doi: 10.1016/j.jorganchem.2004.04.045 – ident: e_1_2_2_56_3 doi: 10.1002/ange.201810798 – ident: e_1_2_2_1_1 – ident: e_1_2_2_29_2 doi: 10.1002/anie.201200223 – ident: e_1_2_2_62_2 doi: 10.1002/asia.201801496 – ident: e_1_2_2_27_1 – ident: e_1_2_2_8_3 doi: 10.1002/ange.19760882103 – ident: e_1_2_2_34_2 doi: 10.1002/anie.201709766 – ident: e_1_2_2_23_2 doi: 10.1039/b210764c – ident: e_1_2_2_30_2 doi: 10.1039/c3ob40137e – ident: e_1_2_2_48_2 doi: 10.1002/cjoc.201600729 – ident: e_1_2_2_25_2 doi: 10.1021/ja204226n – ident: e_1_2_2_61_2 doi: 10.1021/acs.orglett.7b03794 – ident: e_1_2_2_73_1 – ident: e_1_2_2_13_2 doi: 10.1039/b602596j – ident: e_1_2_2_2_2 doi: 10.1002/cber.188401702228 – ident: e_1_2_2_39_2 doi: 10.1002/chem.201304898 – ident: e_1_2_2_9_2 doi: 10.7164/antibiotics.49.50 – ident: e_1_2_2_35_2 doi: 10.1016/j.scib.2019.02.002 – ident: e_1_2_2_17_2 doi: 10.1021/jo00269a001 – ident: e_1_2_2_4_2 doi: 10.1002/352760183X – ident: e_1_2_2_67_2 doi: 10.1021/jm500930h – ident: e_1_2_2_8_2 doi: 10.1002/anie.197606391 – ident: e_1_2_2_29_3 doi: 10.1002/ange.201200223 – ident: e_1_2_2_31_2 doi: 10.1021/cr300503r – ident: e_1_2_2_72_2 doi: 10.1021/acs.orglett.8b02627 – ident: e_1_2_2_33_2 doi: 10.1021/acs.chemrev.6b00057 – ident: e_1_2_2_51_1 doi: 10.1039/C7QO00453B – ident: e_1_2_2_22_3 doi: 10.1002/ange.19961081005 – ident: e_1_2_2_63_2 doi: 10.1021/acs.orglett.9b01416 – ident: e_1_2_2_37_2 doi: 10.1039/C9CC01047E – ident: e_1_2_2_59_1 – ident: e_1_2_2_19_2 doi: 10.1021/jo00083a029 – ident: e_1_2_2_34_3 doi: 10.1002/ange.201709766 – ident: e_1_2_2_14_2 doi: 10.1016/j.tet.2006.05.024 – ident: e_1_2_2_3_2 doi: 10.1002/cber.188401702254 – ident: e_1_2_2_5_1 – ident: e_1_2_2_16_2 doi: 10.1021/ja00362a047 – ident: e_1_2_2_50_3 doi: 10.1002/ange.201809601 – ident: e_1_2_2_21_1 – ident: e_1_2_2_44_2 doi: 10.1039/C8GC03810D – ident: e_1_2_2_76_1 doi: 10.1021/acs.orglett.6b03684 – ident: e_1_2_2_79_2 doi: 10.1021/acs.orglett.7b01162 – ident: e_1_2_2_75_2 doi: 10.1016/j.tetlet.2008.10.139 |
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Snippet | A visible‐light‐induced cascade radical cyclization of aroyl chlorides with 2‐(allyloxy)‐benzaldehyde derivatives has been developed. The method takes... A visible-light-induced cascade radical cyclization of aroyl chlorides with 2-(allyloxy)-benzaldehyde derivatives has been developed. The method takes... |
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SubjectTerms | 1,4-Diketones Acyl radical Benzaldehyde Chemistry Diketones Photoredox catalysis Radical cyclization Synthesis Visible light |
Title | Visible‐Light‐Promoted Cascade Radical Cyclization: Synthesis of 1,4‐Diketones Containing Chroman‐4‐One Skeletons |
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