Enantioselective Copper‐Catalyzed Formal [2+1] and [4+1] Annulations of Diynes with Ketones via Carbonyl Ylides
Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst‐controlled highly...
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Published in | Angewandte Chemie International Edition Vol. 61; no. 43 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
WEINHEIM
Wiley
24.10.2022
Wiley Subscription Services, Inc |
Edition | International ed. in English |
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Abstract | Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst‐controlled highly enantioselective reaction of carbonyl ylides from metal carbenes is extremely challenging. Herein, we report a novel copper‐catalyzed asymmetric formal [2+1] and [4+1] annulations of diynes with ketones via carbonyl ylides. Importantly, this protocol not only represents the first example of successful asymmetric epoxidation via carbonyl ylides, but also constitutes the first reaction of vinyl cations with carbonyl compounds. This method leads to the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities via remote‐stereocontrol strategy.
A copper‐catalyzed asymmetric formal [2+1] and [4+1] annulation of diynes with ketones via carbonyl ylides is disclosed. This protocol enables the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities. |
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AbstractList | Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O-heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst-controlled highly enantioselective reaction of carbonyl ylides from metal carbenes is extremely challenging. Herein, we report a novel copper-catalyzed asymmetric formal [2+1] and [4+1] annulations of diynes with ketones via carbonyl ylides. Importantly, this protocol not only represents the first example of successful asymmetric epoxidation via carbonyl ylides, but also constitutes the first reaction of vinyl cations with carbonyl compounds. This method leads to the divergent, practical and atom-economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities via remote-stereocontrol strategy. Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by the reaction of metal carbenes with carbonyls has attracted increasing attention over the past decades. However, a catalyst‐controlled highly enantioselective reaction of carbonyl ylides from metal carbenes is extremely challenging. Herein, we report a novel copper‐catalyzed asymmetric formal [2+1] and [4+1] annulations of diynes with ketones via carbonyl ylides. Importantly, this protocol not only represents the first example of successful asymmetric epoxidation via carbonyl ylides, but also constitutes the first reaction of vinyl cations with carbonyl compounds. This method leads to the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities via remote‐stereocontrol strategy. A copper‐catalyzed asymmetric formal [2+1] and [4+1] annulation of diynes with ketones via carbonyl ylides is disclosed. This protocol enables the divergent, practical and atom‐economical synthesis of a range of chiral oxiranes and dihydrofurans in moderate to excellent yields with generally excellent enantioselectivities and diastereoselectivities. |
ArticleNumber | 202210637 |
Author | Qi, Lin‐Jun Huang, Zheng‐Qi Jiang, Jia‐Tian Lu, Xin Li, Cui‐Ting Zhu, Xin‐Qi Ye, Long‐Wu |
Author_xml | – sequence: 1 givenname: Lin‐Jun surname: Qi fullname: Qi, Lin‐Jun organization: Taizhou University – sequence: 2 givenname: Cui‐Ting surname: Li fullname: Li, Cui‐Ting organization: Xiamen University – sequence: 3 givenname: Zheng‐Qi surname: Huang fullname: Huang, Zheng‐Qi organization: Xiamen University – sequence: 4 givenname: Jia‐Tian surname: Jiang fullname: Jiang, Jia‐Tian organization: Xiamen University – sequence: 5 givenname: Xin‐Qi surname: Zhu fullname: Zhu, Xin‐Qi organization: Xiamen University – sequence: 6 givenname: Xin surname: Lu fullname: Lu, Xin email: xinlu@xmu.edu.cn organization: Xiamen University – sequence: 7 givenname: Long‐Wu orcidid: 0000-0003-3108-2611 surname: Ye fullname: Ye, Long‐Wu email: longwuye@xmu.edu.cn organization: Chinese Academy of Sciences |
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Cites_doi | 10.1002/ange.201105557 10.1002/anie.202115554 10.1021/ol015600x 10.1016/j.tetlet.2011.02.052 10.1016/j.chempr.2018.02.001 10.1039/D0CS00283F 10.1021/ja00997a060 10.1021/jacs.9b09303 10.1021/acscatal.9b01851 10.1016/S0040-4039(01)01415-0 10.1021/ol016703i 10.1021/om0609970 10.1016/j.xcrp.2021.100448 10.1039/C9CC06078B 10.1002/ange.201100551 10.1002/ange.201700057 10.1002/asia.201403325 10.1002/chem.201502009 10.1021/ja068344y 10.1002/ange.202113464 10.24820/ark.5550190.p010.416 10.1021/jacs.7b12673 10.1021/cs400437s 10.1021/jacs.9b13975 10.1002/anie.201100551 10.1002/anie.201700057 10.1016/j.tetlet.2014.03.105 10.1002/3527607862 10.1016/S0040-4039(00)90743-3 10.1002/ejoc.201001693 10.1002/ange.202115554 10.1002/ange.202007206 10.1055/s-2004-817750 10.1021/acscatal.0c04180 10.1021/ar400193g 10.1002/ange.202204603 10.1002/anie.200800568 10.1002/ange.200602056 10.1016/j.tetlet.2007.11.197 10.1039/D1SC02773E 10.1021/jo049403y 10.1007/s11172-016-1566-x 10.1039/D1NJ02034J 10.1039/D0CS00769B 10.1021/ja00382a038 10.1002/ange.201400241 10.1016/j.tetlet.2018.05.069 10.1039/c3sc50425e 10.1002/anie.201810701 10.1016/j.tet.2008.04.074 10.1021/acs.joc.8b01027 10.1016/S0040-4039(01)88729-3 10.2174/1570193X17999200807141622 10.1039/D0CS00474J 10.1002/ejoc.200500489 10.1021/ar500015k 10.1021/jacs.6b02158 10.1002/ange.202201436 10.1021/acs.chemrev.5b00121 10.1002/ajoc.202000123 10.1039/b816701j 10.2174/1385272819666150810225618 10.1016/j.bmcl.2011.10.127 10.1021/acs.accounts.0c00417 10.1002/anie.201400241 10.1038/s41557-021-00778-z 10.1007/s11426-021-1117-2 10.1002/anie.202007206 10.1002/adsc.201600005 10.1002/anie.202201436 10.1021/ol060266w 10.1002/ange.200800568 10.1002/9783527634880 10.2174/1385272821666170221151356 10.1016/j.tet.2015.06.076 10.1002/anie.202204603 10.1021/cr5006974 10.1021/ol061137i 10.1021/ja0057979 10.1002/anie.201105557 10.1002/anie.200602056 10.1039/C7QO01150D 10.1002/anie.202113464 10.1039/C6CS00023A 10.1021/cs400019u 10.1021/acscatal.6b02929 10.1021/np970030o 10.1002/ange.201810701 10.1021/ar800104y 10.1021/jacs.0c01918 10.1039/c6cs00023a 10.1055/s-2005-871553 10.1039/d1nj02034j 10.1039/c7qo01150d 10.1039/d0cs00474j 10.1039/d0cs00769b 10.1039/c9cc06078b 10.1039/d1sc02773e 10.1039/d0cs00283f |
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Keywords | Heterocycles CARBENOIDS REACTIVITY ALDEHYDES EPOXIDATION CYCLOADDITION EPOXIDES YNAMIDES Asymmetric Catalysis Carbonyl Ylides GENERATION Annulation ACCESS Alkynes DIHYDROFURANS |
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References | 2014 2014; 53 126 2017; 7 2013; 3 2013; 4 2015; 71 2019; 55 2004; 69 2020 2020; 59 132 2011; 52 1982; 104 2022; 65 2018; 83 2008 2008; 47 120 2020; 10 2001; 42 2015; 48 2022 2022; 61 134 2018; 5 2018; 4 2020; 53 2018 2018; 57 130 2020; 9 2020; 49 2016; 358 2008; 64 2012; 22 2014; 55 2007; 26 2016; 45 2001; 123 2019; 9 2007; 129 2021; 45 2018; 140 1997; 60 2021; 2 2011 2020; 142 1967; 89 2017; 21 1969; 10 2015; 10 2006; 8 2014; 47 2006 2005 2004 2003 2017 2017; 56 129 2021; 50 2019; 141 2006 2006; 45 118 2021; 13 1967; 8 2018; 2018 2021; 12 2015; 115 2021; 18 2008; 49 2015; 21 2016; 65 2016; 20 2021 2021; 60 133 2001; 3 2011 2011; 50 123 2016; 138 2009; 38 2018; 59 e_1_2_7_3_2 Li Z.-C. (e_1_2_7_28_2) 2005 e_1_2_7_7_2 e_1_2_7_19_1 e_1_2_7_83_2 e_1_2_7_15_3 e_1_2_7_15_2 e_1_2_7_60_2 e_1_2_7_41_2 e_1_2_7_87_2 e_1_2_7_11_2 e_1_2_7_64_2 e_1_2_7_45_1 e_1_2_7_68_2 e_1_2_7_26_2 e_1_2_7_49_1 e_1_2_7_26_3 Evano G. (e_1_2_7_61_2) 2015; 48 e_1_2_7_90_2 e_1_2_7_94_1 e_1_2_7_71_1 e_1_2_7_52_2 e_1_2_7_75_2 e_1_2_7_23_2 e_1_2_7_33_2 e_1_2_7_56_2 e_1_2_7_79_2 e_1_2_7_37_2 e_1_2_7_4_2 e_1_2_7_8_2 e_1_2_7_16_3 e_1_2_7_16_2 e_1_2_7_82_1 e_1_2_7_40_2 e_1_2_7_86_2 e_1_2_7_63_1 e_1_2_7_12_2 e_1_2_7_44_2 e_1_2_7_67_2 e_1_2_7_67_3 e_1_2_7_48_2 e_1_2_7_48_3 e_1_2_7_29_2 e_1_2_7_70_3 e_1_2_7_93_1 e_1_2_7_70_2 e_1_2_7_24_2 e_1_2_7_51_2 (e_1_2_7_53_3) 2022; 134 e_1_2_7_32_2 e_1_2_7_74_2 e_1_2_7_20_2 e_1_2_7_55_2 e_1_2_7_36_2 e_1_2_7_78_2 e_1_2_7_36_3 e_1_2_7_59_2 e_1_2_7_5_2 (e_1_2_7_65_3) 2022; 134 e_1_2_7_9_2 e_1_2_7_17_2 e_1_2_7_81_2 e_1_2_7_1_1 e_1_2_7_13_2 e_1_2_7_62_2 e_1_2_7_85_1 e_1_2_7_43_2 e_1_2_7_66_2 e_1_2_7_47_2 e_1_2_7_89_2 e_1_2_7_47_3 e_1_2_7_50_2 e_1_2_7_25_2 Garzino F. (e_1_2_7_92_2) 2003 e_1_2_7_77_1 e_1_2_7_31_2 e_1_2_7_73_2 e_1_2_7_54_1 e_1_2_7_96_1 e_1_2_7_21_2 e_1_2_7_35_1 e_1_2_7_58_2 e_1_2_7_39_2 e_1_2_7_2_2 (e_1_2_7_64_3) 2022; 134 e_1_2_7_6_2 e_1_2_7_18_2 e_1_2_7_80_2 e_1_2_7_14_2 e_1_2_7_42_1 e_1_2_7_65_2 e_1_2_7_84_2 e_1_2_7_10_1 e_1_2_7_46_2 e_1_2_7_69_2 e_1_2_7_88_2 e_1_2_7_88_3 e_1_2_7_27_2 e_1_2_7_95_1 e_1_2_7_72_2 e_1_2_7_91_2 e_1_2_7_30_2 e_1_2_7_76_2 e_1_2_7_22_2 e_1_2_7_53_2 e_1_2_7_34_2 e_1_2_7_57_2 e_1_2_7_38_2 Doyle, MP (WOS:000167614600036) 2001; 3 Padwa, A (WOS:000441863800004) 2018 Wang, XN (WOS:000331775200026) 2014; 47 Sahu, SK (WOS:000661178800001) 2021; 45 Lynch, CC (WOS:000596472400006) 2020; 49 Padín, D (WOS:000393539200006) 2017; 7 Muthusamy, S (WOS:000220191700011) 2004 Chen, P.F. (000847820400001.67) 2021; 133 Pettigrew, JD (WOS:000236397000044) 2006; 8 Tindall, DJ (WOS:000424851500043) 2018; 140 Zhang, YQ (WOS:000706045700004) 2021; 13 Braun, I (WOS:000322852900027) 2013; 3 Liu, Y (WOS:000363986500005) 2016; 20 Borrajo-Calleja, GM (WOS:000373518800020) 2016; 138 Kutateladze, AG (WOS:000441112900072) 2018; 83 Zhu, G.-Y. (000847820400001.61) 2022; 61 Wurm, T. (000847820400001.47) 2017; 129 Kim, CH (WOS:000255994700032) 2008; 47 Sartori, SK (WOS:000637314100002) 2021; 18 Wang, ZS (WOS:000515214000046) 2020; 142 Zhang, YQ (WOS:000665056400010) 2021; 2 Davis, RL (WOS:000339564800002) 2014; 53 Dalpozzo, R (WOS:000405956000001) 2017; 21 Geng, Z. (000847820400001.16) 2006; 118 Padwa, A (WOS:000271033400009) 2009; 38 Russell, AE (WOS:000223008100013) 2004; 69 Zhou, B (WOS:000474812400059) 2019; 9 Luo, J (WOS:000598140200022) 2020; 10 Zhu, XQ (WOS:000663879300001) 2021; 12 Zhang, XX (WOS:000428670900002) 2018; 5 Hanari, T (WOS:000359084700007) 2015; 21 Liu, X (WOS:000559994700001) 2020; 59 Li, ZC (WOS:000230448500014) 2005 (WOS:000339885000018) 2011 Doyle, MP (WOS:000172181700035) 2001; 3 Mori, N (WOS:000436221100024) 2018; 59 Celik, MA (WOS:000246764400008) 2007; 26 Wang, Z.-S. (000847820400001.63) 2022; 61 SPENCER, TA (WOS:A19679998200062) 1967; 89 Muthusamy, S (WOS:000358969400021) 2015; 71 Liao, SH (WOS:000340702000004) 2014; 47 Niggemann, M (WOS:000454575500003) 2018; 57 Hong, F.L. (000847820400001.64) 2022; 134 Hong, FL (WOS:000572833000027) 2020; 53 Muthusamy, S (WOS:000290746200027) 2011; 52 Yudin, A.K. (000847820400001.89) 2006 Chen, LF (WOS:000438546100010) 2018; 4 Chen, JR (WOS:000356316300016) 2015; 115 Geng, Z (WOS:000240815100028) 2006; 45 Mejía-Oneto, JM (WOS:000239001500030) 2006; 8 (000847820400001.26) 2011; 123 Hong, FL (WOS:000529156100050) 2020; 142 Bonollo, S (WOS:000290655100001) 2011; 2011 Wood, JL (WOS:000167253200054) 2001; 123 Asiri, AM (WOS:000381438600004) 2016; 45 Wang, HB (WOS:000319940400016) 2013; 4 Chen, PF (WOS:000719981600001) 2021; 60 Hong, F.L. (000847820400001.62) 2022; 134 MURAYAMA, ST (WOS:A1969E511800022) 1969 Wang, Z (WOS:000336114800018) 2014; 55 Chen, YB (WOS:000598713800002) 2020; 49 (000847820400001.86) 2014; 126 Leung, LT (WOS:000351623600032) 2015; 10 Hashmi, ASK (WOS:000333235800015) 2014; 47 Anaç, O (WOS:000253280500032) 2008; 49 Zhou, JL (WOS:000294175700028) 2011; 50 Hong, F.L. (000847820400001.52) 2022; 134 DEMARCH, P (WOS:A1982PF70300038) 1982; 104 Zhang, ZH (WOS:000257500500001) 2008; 64 Liu, X. (000847820400001.71) 2020; 132 Hong, FL (WOS:000492800500051) 2019; 141 Zhou, J.L. (000847820400001.36) 2011; 123 Son, S (WOS:000243840100017) 2007; 129 Zhou, JL (WOS:000317328000031) 2013; 3 Garzino, F (WOS:000181727400023) 2003 Kilroy, TG (WOS:000233713100001) 2005; 2005 Xu, XF (WOS:000297467100020) 2011; 50 Kim, C.H. (000847820400001.14) 2008; 120 Evano, G (WOS:000366962600001) 2015; 48 Day, DP (WOS:000375880200003) 2016; 358 Hong, FL (WOS:000733408800001) 2022; 61 Niggemann, M. (000847820400001.45) 2018; 130 Hu, YC (WOS:000624298500011) 2021; 50 Laha, D (WOS:000525293300001) 2020; 9 Davies, HML (WOS:000171083500005) 2001; 42 OketchRabah, HA (WOS:A1997XA68500006) 1997; 60 Padwa, A (WOS:000400400700008) 2016; 65 Zhao, XM (WOS:000489645500001) 2019; 55 Wurm, T (WOS:000397329300044) 2017; 56 STORM, DL (WOS:A19679319600005) 1967 Sugimoto, K (WOS:000298636700086) 2012; 22 Ford, A (WOS:000361935700007) 2015; 115 |
References_xml | – volume: 142 start-page: 7618 year: 2020 publication-title: J. Am. Chem. Soc. – year: 2011 – volume: 45 118 start-page: 6197 6343 year: 2006 2006 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 65 start-page: 2183 year: 2016 publication-title: Russ. Chem. Bull. – volume: 42 start-page: 6803 year: 2001 publication-title: Tetrahedron Lett. – volume: 53 start-page: 2003 year: 2020 publication-title: Acc. Chem. Res. – volume: 64 start-page: 6577 year: 2008 publication-title: Tetrahedron – volume: 115 start-page: 5301 year: 2015 publication-title: Chem. Rev. – volume: 115 start-page: 9981 year: 2015 publication-title: Chem. Rev. – volume: 10 start-page: 13978 year: 2020 publication-title: ACS Catal. – volume: 60 133 start-page: 27164 27370 year: 2021 2021 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 2 year: 2021 publication-title: Cell Rep. Phys. Sci. – volume: 3 start-page: 1902 year: 2013 publication-title: ACS Catal. – volume: 2018 start-page: 23 year: 2018 publication-title: Arkivoc – volume: 47 120 start-page: 4009 4073 year: 2008 2008 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 3 start-page: 933 year: 2001 publication-title: Org. Lett. – volume: 4 start-page: 1208 year: 2018 publication-title: Chem – volume: 141 start-page: 16961 year: 2019 publication-title: J. Am. Chem. Soc. – volume: 45 start-page: 4471 year: 2016 publication-title: Chem. Soc. Rev. – volume: 45 start-page: 11018 year: 2021 publication-title: New J. Chem. – volume: 140 start-page: 1884 year: 2018 publication-title: J. Am. Chem. Soc. – volume: 3 start-page: 3741 year: 2001 publication-title: Org. Lett. – volume: 13 start-page: 1093 year: 2021 publication-title: Nat. Chem. – start-page: 2587 year: 2011 publication-title: Eur. J. Org. Chem. – volume: 47 start-page: 560 year: 2014 publication-title: Acc. Chem. Res. – start-page: 598 year: 2003 publication-title: Synthesis – volume: 71 start-page: 6219 year: 2015 publication-title: Tetrahedron – volume: 8 start-page: 3275 year: 2006 publication-title: Org. Lett. – volume: 49 start-page: 1062 year: 2008 publication-title: Tetrahedron Lett. – volume: 47 start-page: 864 year: 2014 publication-title: Acc. Chem. Res. – start-page: 4929 year: 2005 publication-title: Eur. J. Org. Chem. – volume: 57 130 start-page: 16942 17186 year: 2018 2018 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 20 start-page: 19 year: 2016 publication-title: Curr. Org. Chem. – start-page: 639 year: 2004 publication-title: Synlett – volume: 49 start-page: 8897 year: 2020 publication-title: Chem. Soc. Rev. – volume: 61 134 year: 2022 2022 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 138 start-page: 4014 year: 2016 publication-title: J. Am. Chem. Soc. – volume: 9 start-page: 6393 year: 2019 publication-title: ACS Catal. – volume: 89 start-page: 5497 year: 1967 publication-title: J. Am. Chem. Soc. – volume: 49 start-page: 8543 year: 2020 publication-title: Chem. Soc. Rev. – volume: 142 start-page: 3636 year: 2020 publication-title: J. Am. Chem. Soc. – volume: 5 start-page: 1092 year: 2018 publication-title: Org. Chem. Front. – volume: 18 start-page: 606 year: 2021 publication-title: Mini-Rev. Org. Chem. – volume: 9 start-page: 918 year: 2020 publication-title: Asian J. Org. Chem. – volume: 60 start-page: 458 year: 1997 publication-title: J. Nat. Prod. – volume: 7 start-page: 992 year: 2017 publication-title: ACS Catal. – volume: 59 start-page: 2600 year: 2018 publication-title: Tetrahedron Lett. – volume: 50 123 start-page: 7874 8020 year: 2011 2011 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 55 start-page: 12127 year: 2019 publication-title: Chem. Commun. – volume: 55 start-page: 2969 year: 2014 publication-title: Tetrahedron Lett. – volume: 69 start-page: 5269 year: 2004 publication-title: J. Org. Chem. – volume: 123 start-page: 2097 year: 2001 publication-title: J. Am. Chem. Soc. – volume: 53 126 start-page: 7406 7534 year: 2014 2014 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 26 start-page: 2978 year: 2007 publication-title: Organometallics – volume: 8 start-page: 1427 year: 2006 publication-title: Org. Lett. – volume: 8 start-page: 1865 year: 1967 publication-title: Tetrahedron Lett. – volume: 12 start-page: 9466 year: 2021 publication-title: Chem. Sci. – volume: 3 start-page: 685 year: 2013 publication-title: ACS Catal. – volume: 129 start-page: 1046 year: 2007 publication-title: J. Am. Chem. Soc. – volume: 52 start-page: 1934 year: 2011 publication-title: Tetrahedron Lett. – volume: 48 start-page: 59 year: 2015 publication-title: Aldrichimica Acta – volume: 21 start-page: 1143 year: 2017 publication-title: Curr. Org. Chem. – volume: 358 start-page: 1368 year: 2016 publication-title: Adv. Synth. Catal. – volume: 59 132 start-page: 17984 18140 year: 2020 2020 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 4 start-page: 2844 year: 2013 publication-title: Chem. Sci. – volume: 10 start-page: 1042 year: 2015 publication-title: Chem. Asian J. – start-page: 1711 year: 2005 publication-title: Synlett – year: 2006 – volume: 104 start-page: 4952 year: 1982 publication-title: J. Am. Chem. Soc. – volume: 47 start-page: 2260 year: 2014 publication-title: Acc. Chem. Res. – volume: 21 start-page: 11671 year: 2015 publication-title: Chem. Eur. J. – volume: 83 start-page: 8341 year: 2018 publication-title: J. Org. Chem. – volume: 10 start-page: 4479 year: 1969 publication-title: Tetrahedron Lett. – volume: 38 start-page: 3072 year: 2009 publication-title: Chem. Soc. Rev. – volume: 56 129 start-page: 3364 3413 year: 2017 2017 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 22 start-page: 449 year: 2012 publication-title: Bioorg. Med. Chem. Lett. – volume: 65 start-page: 20 year: 2022 publication-title: Sci. China Chem. – volume: 50 123 start-page: 11152 11348 year: 2011 2011 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 50 start-page: 2582 year: 2021 publication-title: Chem. Soc. Rev. – ident: e_1_2_7_26_3 doi: 10.1002/ange.201105557 – ident: e_1_2_7_53_2 doi: 10.1002/anie.202115554 – ident: e_1_2_7_32_2 doi: 10.1021/ol015600x – ident: e_1_2_7_27_2 doi: 10.1016/j.tetlet.2011.02.052 – ident: e_1_2_7_96_1 doi: 10.1016/j.chempr.2018.02.001 – ident: e_1_2_7_55_2 doi: 10.1039/D0CS00283F – ident: e_1_2_7_40_2 doi: 10.1021/ja00997a060 – ident: e_1_2_7_50_2 doi: 10.1021/jacs.9b09303 – ident: e_1_2_7_60_2 doi: 10.1021/acscatal.9b01851 – ident: e_1_2_7_31_2 doi: 10.1016/S0040-4039(01)01415-0 – ident: e_1_2_7_33_2 doi: 10.1021/ol016703i – ident: e_1_2_7_38_2 doi: 10.1021/om0609970 – ident: e_1_2_7_10_1 – ident: e_1_2_7_68_2 doi: 10.1016/j.xcrp.2021.100448 – ident: e_1_2_7_72_2 doi: 10.1039/C9CC06078B – ident: e_1_2_7_36_3 doi: 10.1002/ange.201100551 – ident: e_1_2_7_48_3 doi: 10.1002/ange.201700057 – ident: e_1_2_7_13_2 doi: 10.1002/asia.201403325 – ident: e_1_2_7_14_2 doi: 10.1002/chem.201502009 – ident: e_1_2_7_44_2 doi: 10.1021/ja068344y – ident: e_1_2_7_67_3 doi: 10.1002/ange.202113464 – ident: e_1_2_7_54_1 – ident: e_1_2_7_3_2 doi: 10.24820/ark.5550190.p010.416 – ident: e_1_2_7_21_2 doi: 10.1021/jacs.7b12673 – ident: e_1_2_7_76_2 doi: 10.1021/cs400437s – ident: e_1_2_7_69_2 doi: 10.1021/jacs.9b13975 – ident: e_1_2_7_36_2 doi: 10.1002/anie.201100551 – ident: e_1_2_7_45_1 – ident: e_1_2_7_48_2 doi: 10.1002/anie.201700057 – ident: e_1_2_7_24_2 doi: 10.1016/j.tetlet.2014.03.105 – ident: e_1_2_7_91_2 doi: 10.1002/3527607862 – ident: e_1_2_7_41_2 doi: 10.1016/S0040-4039(00)90743-3 – ident: e_1_2_7_71_1 – ident: e_1_2_7_89_2 doi: 10.1002/ejoc.201001693 – volume: 134 start-page: e202115554 year: 2022 ident: e_1_2_7_53_3 publication-title: Angew. Chem. doi: 10.1002/ange.202115554 – ident: e_1_2_7_70_3 doi: 10.1002/ange.202007206 – ident: e_1_2_7_29_2 doi: 10.1055/s-2004-817750 – ident: e_1_2_7_59_2 doi: 10.1021/acscatal.0c04180 – ident: e_1_2_7_62_2 doi: 10.1021/ar400193g – ident: e_1_2_7_77_1 – start-page: 598 year: 2003 ident: e_1_2_7_92_2 publication-title: Synthesis – volume: 134 start-page: e202204603 year: 2022 ident: e_1_2_7_64_3 publication-title: Angew. Chem. doi: 10.1002/ange.202204603 – ident: e_1_2_7_15_2 doi: 10.1002/anie.200800568 – ident: e_1_2_7_16_3 doi: 10.1002/ange.200602056 – ident: e_1_2_7_42_1 – ident: e_1_2_7_37_2 doi: 10.1016/j.tetlet.2007.11.197 – ident: e_1_2_7_52_2 doi: 10.1039/D1SC02773E – ident: e_1_2_7_30_2 doi: 10.1021/jo049403y – ident: e_1_2_7_4_2 doi: 10.1007/s11172-016-1566-x – start-page: 1711 year: 2005 ident: e_1_2_7_28_2 publication-title: Synlett – ident: e_1_2_7_2_2 doi: 10.1039/D1NJ02034J – ident: e_1_2_7_56_2 doi: 10.1039/D0CS00769B – ident: e_1_2_7_34_2 doi: 10.1021/ja00382a038 – ident: e_1_2_7_82_1 – ident: e_1_2_7_88_3 doi: 10.1002/ange.201400241 – ident: e_1_2_7_12_2 doi: 10.1016/j.tetlet.2018.05.069 – ident: e_1_2_7_25_2 doi: 10.1039/c3sc50425e – ident: e_1_2_7_47_2 doi: 10.1002/anie.201810701 – ident: e_1_2_7_9_2 doi: 10.1016/j.tet.2008.04.074 – ident: e_1_2_7_79_2 doi: 10.1021/acs.joc.8b01027 – ident: e_1_2_7_39_2 doi: 10.1016/S0040-4039(01)88729-3 – ident: e_1_2_7_78_2 doi: 10.2174/1570193X17999200807141622 – ident: e_1_2_7_57_2 doi: 10.1039/D0CS00474J – ident: e_1_2_7_81_2 doi: 10.1002/ejoc.200500489 – ident: e_1_2_7_75_2 doi: 10.1021/ar500015k – ident: e_1_2_7_35_1 – ident: e_1_2_7_19_1 – ident: e_1_2_7_49_1 – ident: e_1_2_7_95_1 – ident: e_1_2_7_87_2 doi: 10.1021/jacs.6b02158 – volume: 134 start-page: e202201436 year: 2022 ident: e_1_2_7_65_3 publication-title: Angew. Chem. doi: 10.1002/ange.202201436 – volume: 48 start-page: 59 year: 2015 ident: e_1_2_7_61_2 publication-title: Aldrichimica Acta – ident: e_1_2_7_7_2 doi: 10.1021/acs.chemrev.5b00121 – ident: e_1_2_7_20_2 doi: 10.1002/ajoc.202000123 – ident: e_1_2_7_8_2 doi: 10.1039/b816701j – ident: e_1_2_7_5_2 doi: 10.2174/1385272819666150810225618 – ident: e_1_2_7_83_2 doi: 10.1016/j.bmcl.2011.10.127 – ident: e_1_2_7_58_2 doi: 10.1021/acs.accounts.0c00417 – ident: e_1_2_7_88_2 doi: 10.1002/anie.201400241 – ident: e_1_2_7_66_2 doi: 10.1038/s41557-021-00778-z – ident: e_1_2_7_46_2 doi: 10.1007/s11426-021-1117-2 – ident: e_1_2_7_70_2 doi: 10.1002/anie.202007206 – ident: e_1_2_7_74_2 doi: 10.1002/adsc.201600005 – ident: e_1_2_7_85_1 – ident: e_1_2_7_65_2 doi: 10.1002/anie.202201436 – ident: e_1_2_7_90_2 doi: 10.1021/ol060266w – ident: e_1_2_7_1_1 – ident: e_1_2_7_15_3 doi: 10.1002/ange.200800568 – ident: e_1_2_7_80_2 doi: 10.1002/9783527634880 – ident: e_1_2_7_63_1 – ident: e_1_2_7_86_2 doi: 10.2174/1385272821666170221151356 – ident: e_1_2_7_23_2 doi: 10.1016/j.tet.2015.06.076 – ident: e_1_2_7_64_2 doi: 10.1002/anie.202204603 – ident: e_1_2_7_6_2 doi: 10.1021/cr5006974 – ident: e_1_2_7_17_2 doi: 10.1021/ol061137i – ident: e_1_2_7_18_2 doi: 10.1021/ja0057979 – ident: e_1_2_7_94_1 – ident: e_1_2_7_26_2 doi: 10.1002/anie.201105557 – ident: e_1_2_7_16_2 doi: 10.1002/anie.200602056 – ident: e_1_2_7_11_2 doi: 10.1039/C7QO01150D – ident: e_1_2_7_67_2 doi: 10.1002/anie.202113464 – ident: e_1_2_7_73_2 doi: 10.1039/C6CS00023A – ident: e_1_2_7_43_2 doi: 10.1021/cs400019u – ident: e_1_2_7_22_2 doi: 10.1021/acscatal.6b02929 – ident: e_1_2_7_84_2 doi: 10.1021/np970030o – ident: e_1_2_7_47_3 doi: 10.1002/ange.201810701 – ident: e_1_2_7_93_1 doi: 10.1021/ar800104y – ident: e_1_2_7_51_2 doi: 10.1021/jacs.0c01918 – volume: 61 year: 2022 ident: 000847820400001.63 publication-title: Angew. Chem. Int. Ed – volume: 48 start-page: 59 year: 2015 ident: WOS:000366962600001 article-title: Ynamides: Powerful and Versatile Reagents for Chemical Synthesis publication-title: ALDRICHIMICA ACTA – volume: 89 start-page: 5497 year: 1967 ident: WOS:A19679998200062 article-title: TOTAL SYNTHESIS OF RACEMIC METHYL VINHATICOATE publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 53 start-page: 2003 year: 2020 ident: WOS:000572833000027 article-title: Transition Metal-Catalyzed Tandem Reactions of Ynamides for Divergent N-Heterocycle Synthesis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/acs.accounts.0c00417 – volume: 13 start-page: 1093 year: 2021 ident: WOS:000706045700004 article-title: Asymmetric dearomatization catalysed by chiral Bronsted acids via activation of ynamides publication-title: NATURE CHEMISTRY doi: 10.1038/s41557-021-00778-z – volume: 45 start-page: 6197 year: 2006 ident: WOS:000240815100028 article-title: Total synthesis of pseudolaric acid A publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200602056 – volume: 141 start-page: 16961 year: 2019 ident: WOS:000492800500051 article-title: Generation of Donor/Donor Copper Carbenes through Copper-Catalyzed Diyne Cyclization: Enantioselective and Divergent Synthesis of Chiral Polycyclic Pyrroles publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.9b09303 – volume: 134 year: 2022 ident: 000847820400001.62 publication-title: Angew. Chem – volume: 115 start-page: 9981 year: 2015 ident: WOS:000361935700007 article-title: Modern Organic Synthesis with α-Diazocarbonyl Compounds publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.5b00121 – volume: 358 start-page: 1368 year: 2016 ident: WOS:000375880200003 article-title: Gold-Catalyzed Cycloisomerizations of 1,n-Diyne Carbonates and Esters publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201600005 – volume: 26 start-page: 2978 year: 2007 ident: WOS:000246764400008 article-title: Metal-catalyzed cyclization reactions of carbonyl ylides:: Synthesis and DFT study of mechanisms publication-title: ORGANOMETALLICS doi: 10.1021/om0609970 – volume: 47 start-page: 560 year: 2014 ident: WOS:000331775200026 article-title: Ynamides in Ring Forming Transformations publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar400193g – volume: 45 start-page: 4471 year: 2016 ident: WOS:000381438600004 article-title: Gold-catalysed reactions of diynes publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c6cs00023a – start-page: 1711 year: 2005 ident: WOS:000230448500014 article-title: Rhodium acetate-mediated epoxidation from the reaction of diazobenzyl-phosphonates with aldehydes and a ketone:: A convenient and highly stereoselective synthetic method of cis-1,2-epoxypropylphosphonates publication-title: SYNLETT doi: 10.1055/s-2005-871553 – volume: 64 start-page: 6577 year: 2008 ident: WOS:000257500500001 article-title: Recent studies on the reactions of α-diazocarbonyl compounds publication-title: TETRAHEDRON doi: 10.1016/j.tet.2008.04.074 – volume: 2 start-page: ARTN 100448 year: 2021 ident: WOS:000665056400010 article-title: Rapid and practical access to diverse quindolines by catalyst-free and regioselectivity-reversed Povarov reaction publication-title: CELL REPORTS PHYSICAL SCIENCE doi: 10.1016/j.xcrp.2021.100448 – volume: 8 start-page: 3275 year: 2006 ident: WOS:000239001500030 article-title: Application of the Rh(II) cyclization/cycloaddition cascade for the total synthesis of (±)-aspidophytine publication-title: ORGANIC LETTERS doi: 10.1021/ol061137i – volume: 61 year: 2022 ident: 000847820400001.61 publication-title: Angew. Chem. Int. Ed – start-page: 1 year: 2011 ident: WOS:000339885000018 article-title: Heterocycles in Natural Product Synthesis publication-title: HETEROCYCLES IN NATURAL PRODUCT SYNTHESIS doi: 10.1002/9783527634880 – volume: 59 start-page: 17984 year: 2020 ident: WOS:000559994700001 article-title: Copper-Catalyzed Azide-Ynamide Cyclization to Generate α-Imino Copper Carbenes: Divergent and Enantioselective Access to Polycyclic N-Heterocycles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202007206 – volume: 2011 start-page: 2587 year: 2011 ident: WOS:000290655100001 article-title: Ring-Opening of Epoxides in Water publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.201001693 – volume: 45 start-page: 11018 year: 2021 ident: WOS:000661178800001 article-title: Recent advances in [3+2] cycloaddition of allenes with 1,3-carbonyl ylides; Rh(ii)-catalyzed access to bridged polyoxocarbocyles publication-title: NEW JOURNAL OF CHEMISTRY doi: 10.1039/d1nj02034j – volume: 115 start-page: 5301 year: 2015 ident: WOS:000356316300016 article-title: Formal [4+1] Annulation Reactions in the Synthesis of Carbocyclic and Heterocyclic Systems publication-title: CHEMICAL REVIEWS doi: 10.1021/cr5006974 – volume: 10 start-page: 1042 year: 2015 ident: WOS:000351623600032 article-title: Total Synthesis of (-)-Dolastatrienol publication-title: CHEMISTRY-AN ASIAN JOURNAL doi: 10.1002/asia.201403325 – volume: 5 start-page: 1092 year: 2018 ident: WOS:000428670900002 article-title: Application of a rhodium-catalyzed cyclization cycloaddition cascade strategy to the total synthesis of (-)-curcumol publication-title: ORGANIC CHEMISTRY FRONTIERS doi: 10.1039/c7qo01150d – volume: 47 start-page: 2260 year: 2014 ident: WOS:000340702000004 article-title: Side Arm Strategy for Catalyst Design: Modifying Bisoxazolines for Remote Control of Enantioselection and Related publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar800104y – start-page: 639 year: 2004 ident: WOS:000220191700011 article-title: Stereoselective epoxide generation with cyclic rhodium carbenoids: A new access to spiro-indolooxiranes publication-title: SYNLETT doi: 10.1055/s-2004-817750 – volume: 132 start-page: 18140 year: 2020 ident: 000847820400001.71 publication-title: Angew. Chem – volume: 49 start-page: 8897 year: 2020 ident: WOS:000598713800002 article-title: Bronsted acid-mediated reactions of ynamides publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/d0cs00474j – volume: 4 start-page: 1208 year: 2018 ident: WOS:000438546100010 article-title: Transition-Metal-Catalyzed Intramolecular Nucleophilic Addition of Carbonyl Groups to Alkynes publication-title: CHEM doi: 10.1016/j.chempr.2018.02.001 – volume: 49 start-page: 8543 year: 2020 ident: WOS:000596472400006 article-title: Asymmetric synthesis with ynamides: unique reaction control, chemical diversity and applications publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/d0cs00769b – volume: 49 start-page: 1062 year: 2008 ident: WOS:000253280500032 article-title: Carbonyl ylide reactions of α-benzylidene-β-dicarbonyl compounds:: Competitive formation of dihydrofurans and dihydrobenzoxepines publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2007.11.197 – volume: 120 start-page: 4073 year: 2008 ident: 000847820400001.14 publication-title: Angew. Chem – volume: 59 start-page: 2600 year: 2018 ident: WOS:000436221100024 article-title: Synthetic studies on pseudolaric acid B: Construction of the trans-fused [5-7] ring system via Dieckmann condensation publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2018.05.069 – volume: 42 start-page: 6803 year: 2001 ident: WOS:000171083500005 article-title: Stereoselective synthesis of epoxides by reaction of donor/acceptor-substituted carbenoids with α,β-unsaturated aldehydes publication-title: TETRAHEDRON LETTERS – volume: 3 start-page: 1902 year: 2013 ident: WOS:000322852900027 article-title: Gold Catalysis 2.0 publication-title: ACS CATALYSIS doi: 10.1021/cs400437s – volume: 55 start-page: 12127 year: 2019 ident: WOS:000489645500001 article-title: Dual gold catalysis - an update publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c9cc06078b – volume: 123 start-page: 2097 year: 2001 ident: WOS:000167253200054 article-title: Total synthesis of (±)-epoxysorbicillinol publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 9 start-page: 6393 year: 2019 ident: WOS:000474812400059 article-title: Reversal of Regioselectivity in Ynamide Chemistry publication-title: ACS CATALYSIS doi: 10.1021/acscatal.9b01851 – volume: 52 start-page: 1934 year: 2011 ident: WOS:000290746200027 article-title: Demonstration of 14-20-membered intramolecular carbonyl ylides: diastereoselective synthesis of macrocycles incorporating spiro-indolooxiranes publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2011.02.052 – volume: 56 start-page: 3364 year: 2017 ident: WOS:000397329300044 article-title: On the Gold-Catalyzed Generation of Vinyl Cations from 1,5-Diynes publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201700057 – volume: 140 start-page: 1884 year: 2018 ident: WOS:000424851500043 article-title: Structure and Reactivity of Half-Sandwich Rh(+3) and Ir(+3) Carbene Complexes. Catalytic Metathesis of Azobenzene Derivatives publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.7b12673 – volume: 3 start-page: 933 year: 2001 ident: WOS:000167614600036 article-title: Epoxides and aziridines from diazoacetates via ylide intermediates publication-title: ORGANIC LETTERS doi: 10.1021/ol015600x – volume: 104 start-page: 4952 year: 1982 ident: WOS:A1982PF70300038 article-title: CARBONYL YLIDES FROM ALDEHYDES AND CARBENES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 134 year: 2022 ident: 000847820400001.64 publication-title: Angew. Chem – volume: 18 start-page: 606 year: 2021 ident: WOS:000637314100002 article-title: Sharpless Asymmetric Epoxidation: Applications in the Synthesis of Bioactive Natural Products publication-title: MINI-REVIEWS IN ORGANIC CHEMISTRY doi: 10.2174/1570193X17999200807141622 – start-page: 23 year: 2018 ident: WOS:000441863800004 article-title: Use of nitrogen and oxygen dipole ylides for alkaloid synthesis publication-title: ARKIVOC doi: 10.24820/ark.5550190.p010.416 – volume: 60 start-page: 458 year: 1997 ident: WOS:A1997XA68500006 article-title: Two new antiprotozoal 5-methylcoumarins from Vernonia brachycalyx publication-title: JOURNAL OF NATURAL PRODUCTS – volume: 129 start-page: 3413 year: 2017 ident: 000847820400001.47 publication-title: Angew. Chem – volume: 142 start-page: 7618 year: 2020 ident: WOS:000529156100050 article-title: Copper-Catalyzed Asymmetric Reaction of Alkenyl Diynes with Styrenes by Formal [3+2] Cycloaddition via Cu-Containing AllCarbon 1,3-Dipoles: Access to Chiral Pyrrole-Fused Bridged [2.2.1] Skeletons publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.0c01918 – volume: 118 start-page: 6343 year: 2006 ident: 000847820400001.16 publication-title: Angew. Chem – volume: 50 start-page: 11152 year: 2011 ident: WOS:000297467100020 article-title: Divergent Outcomes of Carbene Transfer Reactions from Dirhodium- and Copper-Based Catalysts Separately or in Combination publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201105557 – volume: 7 start-page: 992 year: 2017 ident: WOS:000393539200006 article-title: [2+1] Cycloaddition of Catalytic Ruthenium Vinyl Carbenes: A Stereoselective Controlled Access to (Z)- and (E)-Vinyl Epoxypyrrolidines publication-title: ACS CATALYSIS doi: 10.1021/acscatal.6b02929 – volume: 47 start-page: 864 year: 2014 ident: WOS:000333235800015 article-title: Dual Gold Catalysis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar500015k – volume: 3 start-page: 685 year: 2013 ident: WOS:000317328000031 article-title: Highly Enantioselective Synthesis of Multifunctionalized Dihydrofurans by Copper-Catalyzed Asymmetric [4+1] Cycloadditions of α-Benzylidene-β-ketoester with Diazo Compound publication-title: ACS CATALYSIS doi: 10.1021/cs400019u – volume: 55 start-page: 2969 year: 2014 ident: WOS:000336114800018 article-title: Oxirane synthesis from diazocarbonyl compounds via NHC-Ag+ catalysis publication-title: TETRAHEDRON LETTERS doi: 10.1016/j.tetlet.2014.03.105 – volume: 71 start-page: 6219 year: 2015 ident: WOS:000358969400021 article-title: 'On-water' generation of carbonyl ylides from diazoamides: rhodium(II) catalyzed synthesis of spiroindolo-oxiranes and -dioxolanes with an interesting diastereoselectivity publication-title: TETRAHEDRON doi: 10.1016/j.tet.2015.06.076 – start-page: 1865 year: 1967 ident: WOS:A19679319600005 article-title: FURAN SYNTHESIS BY 1,4 ADDITION OF CARBOETHOXYCARBENE TO ALPHA-METHOXYMETHYLENE KETONES publication-title: TETRAHEDRON LETTERS – volume: 2005 start-page: 4929 year: 2005 ident: WOS:000233713100001 article-title: Synthesis of dihydrofurans substituted in the 2-position publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ejoc.200500489 – start-page: 4479 year: 1969 ident: WOS:A1969E511800022 article-title: ANOTHER NOVEL FURANOID PRODUCT FROM REACTION OF A 2-METHOXYMETHYLENE KETONE WITH CARBOETHOXYCARBENE publication-title: TETRAHEDRON LETTERS – volume: 126 start-page: 7534 year: 2014 ident: 000847820400001.86 publication-title: Angew. Chem – volume: 50 start-page: 7874 year: 2011 ident: WOS:000294175700028 article-title: Tunable Carbonyl Ylide Reactions: Selective Synthesis of Dihydrofurans and Dihydrobenzoxepines publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201100551 – volume: 57 start-page: 16942 year: 2018 ident: WOS:000454575500003 article-title: Are Vinyl Cations Finally Coming of Age? publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201810701 – volume: 142 start-page: 3636 year: 2020 ident: WOS:000515214000046 article-title: Ynamide Smiles Rearrangement Triggered by Visible-Light-Mediated Regioselective Ketyl-Ynamide Coupling: Rapid Access to Functionalized Indoles and Isoquinolines publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.9b13975 – volume: 3 start-page: 3741 year: 2001 ident: WOS:000172181700035 article-title: Highly stereoselective syntheses of five- and seven-membered ring heterocycles from ylides generated by catalytic reactions of styryldiazoacetates with aldehydes and imines publication-title: ORGANIC LETTERS – volume: 21 start-page: 11671 year: 2015 ident: WOS:000359084700007 article-title: Asymmetric Total Synthesis of (-)-Englerin A through Catalytic Diastereo- and Enantioselective Carbonyl Ylide Cycloaddition publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201502009 – volume: 123 start-page: 8020 year: 2011 ident: 000847820400001.36 publication-title: Angew. Chem – start-page: 598 year: 2003 ident: WOS:000181727400023 article-title: A new entry to functionalized 4-aryl-2-methylenetetralones publication-title: SYNTHESIS-STUTTGART – volume: 138 start-page: 4014 year: 2016 ident: WOS:000373518800020 article-title: Palladium-Catalyzed Enantioselective Intermolecular Carboetherification of Dihydrofurans publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/jacs.6b02158 – volume: 69 start-page: 5269 year: 2004 ident: WOS:000223008100013 article-title: Divergence of carbonyl ylide reactions as a function of diazocarbonyl compound and aldehyde substituent: Dioxolanes, dioxolenes, and epoxides publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo049403y – volume: 8 start-page: 1427 year: 2006 ident: WOS:000236397000044 article-title: Total synthesis of (-)-xyloketal A publication-title: ORGANIC LETTERS doi: 10.1021/ol060266w – volume: 9 start-page: 918 year: 2020 ident: WOS:000525293300001 article-title: Silver-Catalyzed Epoxidation of Aldehydes Using Donor-/ Acceptor-type Vinyl Diazosuccinimides to Access Spiro-Pyrrolidinedioneoxiranes publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ajoc.202000123 – volume: 4 start-page: 2844 year: 2013 ident: WOS:000319940400016 article-title: Rhodium-catalyzed enantioselective cyclopropanation of electron-deficient alkenes publication-title: CHEMICAL SCIENCE doi: 10.1039/c3sc50425e – year: 2006 ident: 000847820400001.89 publication-title: Aziridines and Epoxides in Organic Synthesis – volume: 22 start-page: 449 year: 2012 ident: WOS:000298636700086 article-title: Synthesis of dihydrofuran-fused perhydrophenanthrenes having a phenolic hydroxyl group as a novel anti-Alzheimer's disease agent publication-title: BIOORGANIC & MEDICINAL CHEMISTRY LETTERS doi: 10.1016/j.bmcl.2011.10.127 – volume: 21 start-page: 1143 year: 2017 ident: WOS:000405956000001 article-title: Applications of Chiral Three-membered Rings for Total Synthesis: A Review publication-title: CURRENT ORGANIC CHEMISTRY doi: 10.2174/1385272821666170221151356 – volume: 60 start-page: 27164 year: 2021 ident: WOS:000719981600001 article-title: Bronsted Acid Catalyzed Dearomatization by Intramolecular Hydroalkoxylation/Claisen Rearrangement: Diastereo- and Enantioselective Synthesis of Spirolactams publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202113464 – volume: 130 start-page: 17186 year: 2018 ident: 000847820400001.45 publication-title: Angew. Chem – volume: 133 start-page: 27370 year: 2021 ident: 000847820400001.67 publication-title: Angew. Chem – volume: 47 start-page: 4009 year: 2008 ident: WOS:000255994700032 article-title: A carbonyl ylide cycloaddition approach to platensimycin publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200800568 – volume: 83 start-page: 8341 year: 2018 ident: WOS:000441112900072 article-title: Addressing the Challenges of Structure Elucidation in Natural Products Possessing the Oxirane Moiety publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/acs.joc.8b01027 – volume: 53 start-page: 7406 year: 2014 ident: WOS:000339564800002 article-title: Asymmetric Organocatalytic Epoxidations: Reactions, Scope, Mechanisms, and Applications publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.201400241 – volume: 123 start-page: 11348 year: 2011 ident: 000847820400001.26 publication-title: Angew. Chem – volume: 38 start-page: 3072 year: 2009 ident: WOS:000271033400009 article-title: Domino reactions of rhodium(II) carbenoids for alkaloid synthesis publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/b816701j – volume: 20 start-page: 19 year: 2016 ident: WOS:000363986500005 article-title: Recent Advances in Catalytic Selective Synthesis of Epoxide and Aziridine via Diazocarbonyl Compound publication-title: CURRENT ORGANIC CHEMISTRY doi: 10.2174/1385272819666150810225618 – volume: 134 year: 2022 ident: 000847820400001.52 publication-title: Angew. Chem – volume: 65 start-page: 2183 year: 2016 ident: WOS:000400400700008 article-title: Cycloaddition chemistry of carbonyl ylides for alkaloid synthesis publication-title: RUSSIAN CHEMICAL BULLETIN doi: 10.1007/s11172-016-1566-x – volume: 12 start-page: 9466 year: 2021 ident: WOS:000663879300001 article-title: Copper-catalyzed asymmetric cyclization of alkenyl diynes: method development and new mechanistic insights publication-title: CHEMICAL SCIENCE doi: 10.1039/d1sc02773e – volume: 129 start-page: 1046 year: 2007 ident: WOS:000243840100017 article-title: Copper-catalyzed asymmetric [4+1] cycloadditions of enones with diazo compounds to form dihydrofurans publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja068344y – volume: 10 start-page: 13978 year: 2020 ident: WOS:000598140200022 article-title: Exploiting Remarkable Reactivities of Ynamides: Opportunities in Designing Catalytic Enantioselective Reactions publication-title: ACS CATALYSIS doi: 10.1021/acscatal.0c04180 – volume: 61 start-page: ARTN e202115554 year: 2022 ident: WOS:000733408800001 article-title: Copper-Catalyzed Asymmetric Diyne Cyclization via [1,2]-Stevens-Type Rearrangement for the Synthesis of Chiral Chromeno[3,4-c]pyrroles publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.202115554 – volume: 50 start-page: 2582 year: 2021 ident: WOS:000624298500011 article-title: Reactivity of ynamides in catalytic intermolecular annulations publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/d0cs00283f |
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Snippet | Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O‐heterocycles, and the formation of carbonyl ylides by... Carbonyl ylides have proven to be powerful synthons for the efficient construction of various valuable O-heterocycles, and the formation of carbonyl ylides by... |
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SubjectTerms | Alkynes Annulation Asymmetric Catalysis Asymmetry Carbenes Carbonyl compounds Carbonyl Ylides Carbonyls Catalysts Cations Chemistry Chemistry, Multidisciplinary Copper Divergence Enantiomers Epoxidation Heterocycles Ketones Physical Sciences Science & Technology |
Title | Enantioselective Copper‐Catalyzed Formal [2+1] and [4+1] Annulations of Diynes with Ketones via Carbonyl Ylides |
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