8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)–H disulfenylation of o -carboranes
A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)–H disulfenylation of o -carboranes has been achieved, leading to a series of B(4,5)–disulfenylated o -carborane derivatives in high yields with excellent regioselectivity. The in situ departure of the 8-aminoquinoline b...
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| Published in | Chemical communications (Cambridge, England) Vol. 56; no. 85; pp. 12997 - 13000 |
|---|---|
| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
Cambridge
Royal Society of Chemistry
27.10.2020
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1359-7345 1364-548X 1364-548X |
| DOI | 10.1039/D0CC05207H |
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| Abstract | A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)–H disulfenylation of
o
-carboranes has been achieved, leading to a series of B(4,5)–disulfenylated
o
-carborane derivatives in high yields with excellent regioselectivity. The
in situ
departure of the 8-aminoquinoline bidentate auxiliary circumvents additional processes for directing group removal, thus enhancing the atom-/step-economy. |
|---|---|
| AbstractList | A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)–H disulfenylation of o-carboranes has been achieved, leading to a series of B(4,5)–disulfenylated o-carborane derivatives in high yields with excellent regioselectivity. The in situ departure of the 8-aminoquinoline bidentate auxiliary circumvents additional processes for directing group removal, thus enhancing the atom-/step-economy. A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)-H disulfenylation of o-carboranes has been achieved, leading to a series of B(4,5)-disulfenylated o-carborane derivatives in high yields with excellent regioselectivity. The in situ departure of the 8-aminoquinoline bidentate auxiliary circumvents additional processes for directing group removal, thus enhancing the atom-/step-economy.A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)-H disulfenylation of o-carboranes has been achieved, leading to a series of B(4,5)-disulfenylated o-carborane derivatives in high yields with excellent regioselectivity. The in situ departure of the 8-aminoquinoline bidentate auxiliary circumvents additional processes for directing group removal, thus enhancing the atom-/step-economy. A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)–H disulfenylation of o -carboranes has been achieved, leading to a series of B(4,5)–disulfenylated o -carborane derivatives in high yields with excellent regioselectivity. The in situ departure of the 8-aminoquinoline bidentate auxiliary circumvents additional processes for directing group removal, thus enhancing the atom-/step-economy. |
| Author | Chen, Yu Quan, Yangjian Xie, Zuowei |
| Author_xml | – sequence: 1 givenname: Yu orcidid: 0000-0002-7049-1285 surname: Chen fullname: Chen, Yu organization: Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, N.T., China – sequence: 2 givenname: Yangjian orcidid: 0000-0002-6500-3152 surname: Quan fullname: Quan, Yangjian organization: Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, N.T., China – sequence: 3 givenname: Zuowei orcidid: 0000-0001-6206-004X surname: Xie fullname: Xie, Zuowei organization: Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong, Shatin, N.T., China |
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| Cites_doi | 10.1002/chem.201701965 10.1002/anie.201109069 10.1002/chem.201705025 10.1021/cr2000866 10.1021/jacs.7b07160 10.1039/C8CC08693A 10.1007/978-3-319-24630-7 10.1007/s11426-018-9388-3 10.1002/chem.201905647 10.1002/adma.201704238 10.1002/anie.201914500 10.1021/ar5004626 10.1021/acs.chemrev.6b00772 10.1021/ar010146i 10.1039/C9DT01140D 10.1002/cjoc.201900475 10.1038/nchem.2686 10.1021/ja1045378 10.1002/chem.202000549 10.1021/cr200038x 10.1021/jacs.0c02228 10.1126/science.1138690 10.1039/C5CC03608A 10.1002/1521-3773(20020816)41:16<2991::AID-ANIE2991>3.0.CO;2-6 10.1021/ja203367h 10.1021/jacs.8b07872 10.1002/chem.201600510 10.1039/C9DT04553H 10.1039/D0CC02531C 10.1039/C7QO01016H 10.1021/acs.jmedchem.5b01932 10.1021/acs.chemrev.8b00551 10.1002/chem.201704937 10.1002/asia.202000642 10.1021/acs.inorgchem.8b00038 10.1021/jacs.8b01754 10.1039/C6CC06200H 10.1021/jacs.8b08826 10.1016/j.ccr.2013.02.004 10.1039/C9CS00169G 10.1021/acs.accounts.5b00134 10.1021/cr068440h 10.1021/cr980442h 10.1021/ja3092278 10.1021/jacs.8b01896 10.1016/j.ccr.2017.11.006 10.1039/b904403e 10.1021/jacs.8b00605 10.1038/s41563-018-0021-9 10.1021/jacs.6b05172 10.1039/c3sc21818j 10.1021/ar100156f 10.1021/jacs.0c02490 10.1021/jacs.9b06204 10.1039/D0OB00698J 10.1021/acs.chemrev.6b00198 10.1021/jacs.7b04080 10.1039/d0sc01515f 10.1002/chem.201705181 10.1002/anie.201807664 10.1039/C3CS60440C 10.1021/cr00091a001 10.1039/C5CC08213G 10.1021/jacs.0c02121 10.1021/cr500410y 10.1021/jacs.0c00300 10.1021/jacs.9b00302 10.1021/ic50062a038 10.1021/acs.orglett.9b03790 10.1038/ncomms14827 10.1021/acs.chemrev.9b00495 10.1039/c39890001633 |
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| References | Zhang (D0CC05207H-(cit15d)/*[position()=1]) 2018; 140 Au (D0CC05207H-(cit12b)/*[position()=1]) 2020; 142 Poater (D0CC05207H-(cit6a)/*[position()=1]) 2020; 142 Kung (D0CC05207H-(cit5d)/*[position()=1]) 2018; 140 Poater (D0CC05207H-(cit6b)/*[position()=1]) 2016; 22 Au (D0CC05207H-(cit8j)/*[position()=1]) 2020; 15 Au (D0CC05207H-(cit8g)/*[position()=1]) 2019; 141 Quan (D0CC05207H-(cit7b)/*[position()=1]) 2018; 24 Hawthorne (D0CC05207H-(cit2a)/*[position()=1]) 1999; 99 Dziedzic (D0CC05207H-(cit9f)/*[position()=1]) 2017; 139 Dixneuf (D0CC05207H-(cit11a)/*[position()=1]) 2016 Willert-Porada (D0CC05207H-(cit17b)/*[position()=1]) 1989 Saha (D0CC05207H-(cit4c)/*[position()=1]) 2017; 29 Cheng (D0CC05207H-(cit8e)/*[position()=1]) 2020; 26 Chen (D0CC05207H-(cit8i)/*[position()=1]) 2020; 56 Liang (D0CC05207H-(cit9j)/*[position()=1]) 2020 Tran (D0CC05207H-(cit16a)/*[position()=1]) 2012; 134 Guo (D0CC05207H-(cit5c)/*[position()=1]) 2015; 51 Lin (D0CC05207H-(cit9d)/*[position()=1]) 2018; 140 Hirschbeck (D0CC05207H-(cit10c)/*[position()=1]) 2018; 24 Daugulis (D0CC05207H-(cit11b)/*[position()=1]) 2015; 48 Wee (D0CC05207H-(cit5e)/*[position()=1]) 2012; 51 Guo (D0CC05207H-(cit11e)/*[position()=1]) 2015; 115 Cheng (D0CC05207H-(cit8b)/*[position()=1]) 2018; 140 Koshino (D0CC05207H-(cit5b)/*[position()=1]) 2007; 316 Zhang (D0CC05207H-(cit9l)/*[position()=1]) 2020; 18 Xu (D0CC05207H-(cit9c)/*[position()=1]) 2019; 21 Quan (D0CC05207H-(cit7a)/*[position()=1]) 2019; 48 Zhang (D0CC05207H-(cit9e)/*[position()=1]) 2017; 139 DuBois (D0CC05207H-(cit10a)/*[position()=1]) 1989; 89 Xiong (D0CC05207H-(cit16d)/*[position()=1]) 2018; 5 Rej (D0CC05207H-(cit13)/*[position()=1]) 2020; 120 Zhang (D0CC05207H-(cit9k)/*[position()=1]) 2020; 26 Zhang (D0CC05207H-(cit7c)/*[position()=1]) 2019; 378 Chen (D0CC05207H-(cit12a)/*[position()=1]) 2019; 62 Quan (D0CC05207H-(cit7d)/*[position()=1]) 2019; 48 Grimes (D0CC05207H-(cit1a)/*[position()=1]) 2016 Cheng (D0CC05207H-(cit8a)/*[position()=1]) 2017; 8 Couto (D0CC05207H-(cit2e)/*[position()=1]) 2017; 23 Xu (D0CC05207H-(cit14)/*[position()=1]) 2018; 57 Leśnikowski (D0CC05207H-(cit2d)/*[position()=1]) 2016; 59 Dziedzic (D0CC05207H-(cit7e)/*[position()=1]) 2019; 55 Shang (D0CC05207H-(cit11c)/*[position()=1]) 2017; 117 Xu (D0CC05207H-(cit9b)/*[position()=1]) 2018; 57 King (D0CC05207H-(cit15a)/*[position()=1]) 2010; 132 Chirik (D0CC05207H-(cit11d)/*[position()=1]) 2015; 48 Srogl (D0CC05207H-(cit16b)/*[position()=1]) 2009 Jung (D0CC05207H-(cit4d)/*[position()=1]) 2018; 17 Mills (D0CC05207H-(cit9h)/*[position()=1]) 2020; 142 Lyu (D0CC05207H-(cit8c)/*[position()=1]) 2019; 141 Issa (D0CC05207H-(cit2c)/*[position()=1]) 2011; 111 Cui (D0CC05207H-(cit8f)/*[position()=1]) 2020; 49 Yao (D0CC05207H-(cit3c)/*[position()=1]) 2013; 257 Núñez (D0CC05207H-(cit5a)/*[position()=1]) 2016; 116 Qian (D0CC05207H-(cit4b)/*[position()=1]) 2017; 9 Scholz (D0CC05207H-(cit2b)/*[position()=1]) 2011; 111 Xie (D0CC05207H-(cit3b)/*[position()=1]) 2003; 36 Mellah (D0CC05207H-(cit10b)/*[position()=1]) 2007; 107 Mukherjee (D0CC05207H-(cit4a)/*[position()=1]) 2016; 52 Ribas (D0CC05207H-(cit15c)/*[position()=1]) 2002; 41 Hosmane (D0CC05207H-(cit1b)/*[position()=1]) 2011 Ge (D0CC05207H-(cit8d)/*[position()=1]) 2020; 59 Eleazer (D0CC05207H-(cit9g)/*[position()=1]) 2016; 138 Kim (D0CC05207H-(cit15b)/*[position()=1]) 2018; 140 Izatt (D0CC05207H-(cit11f)/*[position()=1]) 2014; 43 Beurskens (D0CC05207H-(cit17a)/*[position()=1]) 1968; 7 Couto (D0CC05207H-(cit2f)/*[position()=1]) 2018; 24 Au (D0CC05207H-(cit8h)/*[position()=1]) 2020; 38 Fisher (D0CC05207H-(cit3a)/*[position()=1]) 2019; 119 Baek (D0CC05207H-(cit9i)/*[position()=1]) 2020; 142 Cao (D0CC05207H-(cit9a)/*[position()=1]) 2016; 52 Cioran (D0CC05207H-(cit4e)/*[position()=1]) 2012; 134 Casitas (D0CC05207H-(cit16c)/*[position()=1]) 2013; 4 Qiu (D0CC05207H-(cit3d)/*[position()=1]) 2011; 44 |
| References_xml | – volume: 23 start-page: 9233 year: 2017 ident: D0CC05207H-(cit2e)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.201701965 – volume: 51 start-page: 2677 year: 2012 ident: D0CC05207H-(cit5e)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201109069 – volume: 24 start-page: 7092 year: 2018 ident: D0CC05207H-(cit10c)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.201705025 – volume: 111 start-page: 5701 year: 2011 ident: D0CC05207H-(cit2c)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr2000866 – volume: 139 start-page: 14511 year: 2017 ident: D0CC05207H-(cit9e)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.7b07160 – volume: 55 start-page: 430 year: 2019 ident: D0CC05207H-(cit7e)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C8CC08693A – volume-title: Topics in Organometallic Chemistry: C–H Bond Activation and Catalytic Functionalization II year: 2016 ident: D0CC05207H-(cit11a)/*[position()=1] doi: 10.1007/978-3-319-24630-7 – volume: 62 start-page: 74 year: 2019 ident: D0CC05207H-(cit12a)/*[position()=1] publication-title: Sci. China: Chem. doi: 10.1007/s11426-018-9388-3 – volume: 26 start-page: 5037 year: 2020 ident: D0CC05207H-(cit9k)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.201905647 – volume: 29 start-page: 1704238 year: 2017 ident: D0CC05207H-(cit4c)/*[position()=1] publication-title: Adv. Mater. doi: 10.1002/adma.201704238 – volume: 59 start-page: 4851 year: 2020 ident: D0CC05207H-(cit8d)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201914500 – volume: 48 start-page: 1053 year: 2015 ident: D0CC05207H-(cit11b)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar5004626 – volume: 117 start-page: 9086 year: 2017 ident: D0CC05207H-(cit11c)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.6b00772 – volume: 36 start-page: 1 year: 2003 ident: D0CC05207H-(cit3b)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar010146i – volume: 48 start-page: 7494 year: 2019 ident: D0CC05207H-(cit7d)/*[position()=1] publication-title: Dalton Trans. doi: 10.1039/C9DT01140D – volume: 38 start-page: 383 year: 2020 ident: D0CC05207H-(cit8h)/*[position()=1] publication-title: Chin. J. Chem. doi: 10.1002/cjoc.201900475 – volume: 9 start-page: 333 year: 2017 ident: D0CC05207H-(cit4b)/*[position()=1] publication-title: Nat. Chem. doi: 10.1038/nchem.2686 – volume: 132 start-page: 12068 year: 2010 ident: D0CC05207H-(cit15a)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja1045378 – volume: 26 start-page: 7212 year: 2020 ident: D0CC05207H-(cit8e)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.202000549 – volume: 111 start-page: 7035 year: 2011 ident: D0CC05207H-(cit2b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr200038x – volume: 142 start-page: 9396 year: 2020 ident: D0CC05207H-(cit6a)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.0c02228 – volume: 316 start-page: 853 year: 2007 ident: D0CC05207H-(cit5b)/*[position()=1] publication-title: Science doi: 10.1126/science.1138690 – volume: 51 start-page: 12004 year: 2015 ident: D0CC05207H-(cit5c)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C5CC03608A – volume: 41 start-page: 2991 year: 2002 ident: D0CC05207H-(cit15c)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/1521-3773(20020816)41:16<2991::AID-ANIE2991>3.0.CO;2-6 – volume: 134 start-page: 212 year: 2012 ident: D0CC05207H-(cit4e)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja203367h – volume: 140 start-page: 13798 year: 2018 ident: D0CC05207H-(cit9d)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b07872 – volume: 22 start-page: 7437 year: 2016 ident: D0CC05207H-(cit6b)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.201600510 – volume: 49 start-page: 1380 year: 2020 ident: D0CC05207H-(cit8f)/*[position()=1] publication-title: Dalton Trans. doi: 10.1039/C9DT04553H – volume: 56 start-page: 7001 year: 2020 ident: D0CC05207H-(cit8i)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/D0CC02531C – volume: 5 start-page: 982 year: 2018 ident: D0CC05207H-(cit16d)/*[position()=1] publication-title: Org. Chem. Front. doi: 10.1039/C7QO01016H – volume: 59 start-page: 7738 year: 2016 ident: D0CC05207H-(cit2d)/*[position()=1] publication-title: J. Med. Chem. doi: 10.1021/acs.jmedchem.5b01932 – volume: 119 start-page: 8262 year: 2019 ident: D0CC05207H-(cit3a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.8b00551 – volume: 24 start-page: 2795 year: 2018 ident: D0CC05207H-(cit7b)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.201704937 – volume: 15 start-page: 2170 year: 2020 ident: D0CC05207H-(cit8j)/*[position()=1] publication-title: Chem. – Asian J. doi: 10.1002/asia.202000642 – volume-title: Carboranes year: 2016 ident: D0CC05207H-(cit1a)/*[position()=1] – volume: 57 start-page: 2925 year: 2018 ident: D0CC05207H-(cit9b)/*[position()=1] publication-title: Inorg. Chem. doi: 10.1021/acs.inorgchem.8b00038 – volume-title: Boron Science: New Technologies and Applications year: 2011 ident: D0CC05207H-(cit1b)/*[position()=1] – volume: 140 start-page: 4508 year: 2018 ident: D0CC05207H-(cit8b)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b01754 – volume: 52 start-page: 11446 year: 2016 ident: D0CC05207H-(cit9a)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C6CC06200H – volume: 140 start-page: 14350 year: 2018 ident: D0CC05207H-(cit15b)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b08826 – volume: 257 start-page: 2522 year: 2013 ident: D0CC05207H-(cit3c)/*[position()=1] publication-title: Coord. Chem. Rev. doi: 10.1016/j.ccr.2013.02.004 – volume: 48 start-page: 3660 year: 2019 ident: D0CC05207H-(cit7a)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/C9CS00169G – volume: 48 start-page: 1687 year: 2015 ident: D0CC05207H-(cit11d)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/acs.accounts.5b00134 – volume: 107 start-page: 5133 year: 2007 ident: D0CC05207H-(cit10b)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr068440h – volume: 99 start-page: 3421 year: 1999 ident: D0CC05207H-(cit2a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr980442h – volume: 134 start-page: 18237 year: 2012 ident: D0CC05207H-(cit16a)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/ja3092278 – volume: 140 start-page: 5579 year: 2018 ident: D0CC05207H-(cit15d)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b01896 – volume: 378 start-page: 466 year: 2019 ident: D0CC05207H-(cit7c)/*[position()=1] publication-title: Coord. Chem. Rev. doi: 10.1016/j.ccr.2017.11.006 – start-page: 3463 year: 2009 ident: D0CC05207H-(cit16b)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/b904403e – volume: 140 start-page: 3871 year: 2018 ident: D0CC05207H-(cit5d)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.8b00605 – volume: 17 start-page: 341 year: 2018 ident: D0CC05207H-(cit4d)/*[position()=1] publication-title: Nat. Mater. doi: 10.1038/s41563-018-0021-9 – volume: 138 start-page: 10531 year: 2016 ident: D0CC05207H-(cit9g)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.6b05172 – volume: 4 start-page: 2301 year: 2013 ident: D0CC05207H-(cit16c)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/c3sc21818j – volume: 44 start-page: 299 year: 2011 ident: D0CC05207H-(cit3d)/*[position()=1] publication-title: Acc. Chem. Res. doi: 10.1021/ar100156f – volume: 142 start-page: 6940 year: 2020 ident: D0CC05207H-(cit12b)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.0c02490 – volume: 141 start-page: 12855 year: 2019 ident: D0CC05207H-(cit8g)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.9b06204 – volume: 18 start-page: 4723 year: 2020 ident: D0CC05207H-(cit9l)/*[position()=1] publication-title: Org. Biomol. Chem. doi: 10.1039/D0OB00698J – volume: 116 start-page: 14307 year: 2016 ident: D0CC05207H-(cit5a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.6b00198 – volume: 139 start-page: 7729 year: 2017 ident: D0CC05207H-(cit9f)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.7b04080 – year: 2020 ident: D0CC05207H-(cit9j)/*[position()=1] publication-title: Chem. Sci. doi: 10.1039/d0sc01515f – volume: 24 start-page: 3122 year: 2018 ident: D0CC05207H-(cit2f)/*[position()=1] publication-title: Chem. – Eur. J. doi: 10.1002/chem.201705181 – volume: 57 start-page: 11797 year: 2018 ident: D0CC05207H-(cit14)/*[position()=1] publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201807664 – volume: 43 start-page: 2451 year: 2014 ident: D0CC05207H-(cit11f)/*[position()=1] publication-title: Chem. Soc. Rev. doi: 10.1039/C3CS60440C – volume: 89 start-page: 1 year: 1989 ident: D0CC05207H-(cit10a)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr00091a001 – volume: 52 start-page: 1070 year: 2016 ident: D0CC05207H-(cit4a)/*[position()=1] publication-title: Chem. Commun. doi: 10.1039/C5CC08213G – volume: 142 start-page: 9890 year: 2020 ident: D0CC05207H-(cit9i)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.0c02121 – volume: 115 start-page: 1622 year: 2015 ident: D0CC05207H-(cit11e)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/cr500410y – volume: 142 start-page: 4586 year: 2020 ident: D0CC05207H-(cit9h)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.0c00300 – volume: 141 start-page: 4219 year: 2019 ident: D0CC05207H-(cit8c)/*[position()=1] publication-title: J. Am. Chem. Soc. doi: 10.1021/jacs.9b00302 – volume: 7 start-page: 810 year: 1968 ident: D0CC05207H-(cit17a)/*[position()=1] publication-title: Inorg. Chem. doi: 10.1021/ic50062a038 – volume: 21 start-page: 9276 year: 2019 ident: D0CC05207H-(cit9c)/*[position()=1] publication-title: Org. Lett. doi: 10.1021/acs.orglett.9b03790 – volume: 8 start-page: 14827 year: 2017 ident: D0CC05207H-(cit8a)/*[position()=1] publication-title: Nat. Commun. doi: 10.1038/ncomms14827 – volume: 120 start-page: 1788 year: 2020 ident: D0CC05207H-(cit13)/*[position()=1] publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.9b00495 – start-page: 1633 year: 1989 ident: D0CC05207H-(cit17b)/*[position()=1] publication-title: J. Chem. Soc., Chem. Commun. doi: 10.1039/c39890001633 |
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-carboranes has been achieved, leading to a series of... A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)–H disulfenylation of o-carboranes has been achieved, leading to a series of... A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)-H disulfenylation of o-carboranes has been achieved, leading to a series of... |
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| SubjectTerms | Aminoquinolines cages Carborane Copper Crystallography NMR Nuclear magnetic resonance Organometallic compounds Regioselectivity |
| Title | 8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)–H disulfenylation of o -carboranes |
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