Chinese Journal of Organic Chemistry ›› 2022, Vol. 42 ›› Issue (5): 1265-1285.DOI: 10.6023/cjoc202111001 Previous Articles Next Articles
Special Issue: 有机氟化学虚拟合辑
REVIEWS
收稿日期:
2021-11-01
修回日期:
2022-01-14
发布日期:
2022-02-17
通讯作者:
牛丽亚, 杨清正
基金资助:
Bin-Kai Liu, Kun-Xu Teng, Li-Ya Niu(), Qing-Zheng Yang()
Received:
2021-11-01
Revised:
2022-01-14
Published:
2022-02-17
Contact:
Li-Ya Niu, Qing-Zheng Yang
Supported by:
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Bin-Kai Liu, Kun-Xu Teng, Li-Ya Niu, Qing-Zheng Yang. Progress in the Synthesis of Boron Dipyrromethene (BODIPY) Fluorescent Dyes[J]. Chinese Journal of Organic Chemistry, 2022, 42(5): 1265-1285.
[1] |
Loudet, A.; Burgess, K. Chem. Rev. 2007, 107, 4891.
doi: 10.1021/cr078381n |
[2] |
Ulrich, G.; Ziessel, R.; Harriman, A. Angew. Chem., Int. Ed. 2008, 47, 1184.
doi: 10.1002/anie.200702070 |
[3] |
Zheng, H.; Zhan, X. Q.; Bian, Q. N.; Zhang, X. J. Chem. Commun. 2013, 49, 429.
doi: 10.1039/C2CC35997A |
[4] |
Yan, F.; Fan, K.; Bai, Z.; Zhang, R.; Zu, F.; Xu, J.; Li, X. TrAC, Trends Anal. Chem. 2017, 97, 15.
doi: 10.1016/j.trac.2017.08.013 |
[5] |
Cao, D.; Liu, Z.; Verwilst, P.; Koo, S.; Jangjili, P.; Kim, J. S.; Lin, W. Chem. Rev. 2019, 119, 10403.
doi: 10.1021/acs.chemrev.9b00145 |
[6] |
Beija, M.; Afonso, C. A. M.; Martinho, J. M. G. Chem. Soc. Rev. 2009, 38, 2410.
doi: 10.1039/b901612k |
[7] |
Shindy, H. A. Dyes Pigm. 2017, 145, 505.
doi: 10.1016/j.dyepig.2017.06.029 |
[8] |
Guo, X.; Facchetti, A.; Marks, T. J. Chem. Rev. 2014, 114, 8943.
doi: 10.1021/cr500225d |
[9] |
Li, C.; Wonneberger, H. Adv. Mater. 2012, 24, 613.
doi: 10.1002/adma.201104447 |
[10] |
Chen, S.; Slattum, P.; Wang, C. Y.; Zang, L. Chem. Rev. 2015, 115, 11967.
doi: 10.1021/acs.chemrev.5b00312 |
[11] |
Jiang, C.; Huang, H.; Kang, X.; Yang, L.; Xi, Z.; Sun, H.; Pluth, M. D.; Yi, L. Chem. Soc. Rev. 2021, 50, 7436.
doi: 10.1039/D0CS01096K |
[12] |
Boens, N.; Leen, V.; Dehaen, W. Chem. Soc. Rev. 2012, 41, 1130.
doi: 10.1039/c1cs15132k pmid: 21796324 |
[13] |
Ni, Y.; Wu, J. Org. Biomol. Chem. 2014, 12, 3774.
doi: 10.1039/c3ob42554a |
[14] |
Kowada, T.; Maeda, H.; Kikuchi, K. Chem. Soc. Rev. 2015, 44, 4953.
doi: 10.1039/C5CS00030K |
[15] |
Shah, M.; Thangaraj, K.; Soong, M.-L.; Wolford, L. T.; Boyer, J. H.; Politzer, I. R.; Pavlopoulos, T. G. Heteroat. Chem. 1990, 1, 389.
doi: 10.1002/hc.520010507 |
[16] |
Awuah, S. G.; You, Y. RSC Adv. 2012, 2, 11169.
doi: 10.1039/c2ra21404k |
[17] |
Kamkaew, A.; Lim, S. H.; Lee, H. B.; Kiew, L. V.; Chung, L. Y.; Burgess, K. Chem. Soc. Rev. 2013, 42, 77.
doi: 10.1039/C2CS35216H |
[18] |
Zhao, J.; Xu, K.; Yang, W.; Wang, Z.; Zhong, F. Chem. Soc. Rev. 2015, 44, 8904.
doi: 10.1039/C5CS00364D |
[19] |
Singh, S. P.; Gayathri, T. Eur. J. Org. Chem. 2014, 2014, 4689.
doi: 10.1002/ejoc.201400093 |
[20] |
Yuan, B.; Wang, H.; Xu, J.-F.; Zhang, X. ACS Appl. Mater. Interfaces 2020, 12, 26982.
doi: 10.1021/acsami.0c07471 |
[21] |
Yuan, B.; Wu, H.; Wang, H.; Tang, B.; Xu, J.-F.; Zhang, X. Angew. Chem., Int. Ed. 2021, 60, 706.
doi: 10.1002/anie.202012477 |
[22] |
Treibs, A.; Kreuzer, F.-H. Justus Liebigs Ann. Chem. 1968, 718, 208.
doi: 10.1002/jlac.19687180119 |
[23] |
Wories, H. J.; Koek, J. H.; Lodder, G.; Lugtenburg, J.; Fokkens, R.; Driessen, O.; Mohn, G. R. Recl. Trav. Chim. Pays-Bas 1985, 104, 288.
doi: 10.1002/recl.19851041104 |
[24] |
Bañuelos-Prieto, J.; Agarrabeitia, A. R.; Garcia-Moreno, I.; Lopez-Arbeloa, I.; Costela, A.; Infantes, L.; Perez-Ojeda, M. E.; Palacios-Cuesta, M.; Ortiz, M. J. Chem.-Eur. J. 2010, 16, 14094.
doi: 10.1002/chem.201002095 pmid: 20960443 |
[25] |
Zhang, M.; Hao, E.; Zhou, J.; Yu, C.; Bai, G.; Wang, F.; Jiao, L. Org. Biomol. Chem. 2012, 10, 2139.
doi: 10.1039/c2ob06689k pmid: 22302220 |
[26] |
Lindsey, J. S.; Schreiman, I. C.; Hsu, H. C.; Kearney, P. C.; Marguerettaz, A. M. J. Org. Chem. 1987, 52, 827.
doi: 10.1021/jo00381a022 |
[27] |
Baruah, M.; Qin, W. W.; Basaric, N.; De Borggraeve, W. M.; Boens, N. J. Org. Chem. 2005, 70, 4152.
doi: 10.1021/jo0503714 |
[28] |
Duran-Sampedro, G.; Agarrabeitia, A. R.; Garcia-Moreno, I.; Costela, A.; Bañuelos, J.; Arbeloa, T.; López Arbeloa, I.; Chiara, J. L.; Ortiz, M. J. Eur. J. Org. Chem. 2012, 2012, 6335.
doi: 10.1002/ejoc.201200946 |
[29] |
Zhou, X.; Yu, C.; Feng, Z.; Yu, Y.; Wang, J.; Hao, E.; Wei, Y.; Mu, X.; Jiao, L. Org. Lett. 2015, 17, 4632.
doi: 10.1021/acs.orglett.5b02383 pmid: 26340068 |
[30] |
Frank, F.; Alice, L. M.; Mauker, P.; Alsimaree, A. A.; Waddell, P. G.; Probert, M. R.; Penfold, T. J.; Knight, J. G.; Hall, M. J. Tetrahedron 2020, 76, 131113.
doi: 10.1016/j.tet.2020.131113 |
[31] |
Satoh, T.; Fujii, K.; Kimura, Y.; Matano, Y. J. Org. Chem. 2018, 83, 5274.
doi: 10.1021/acs.joc.8b00087 |
[32] |
Cao, T.; Gong, D.; Zheng, L.; Wang, J.; Qian, J.; Liu, W.; Cao, Y.; Iqbal, K.; Qin, W.; Iqbal, A. Anal. Chim. Acta 2019, 1078, 168.
doi: 10.1016/j.aca.2019.06.033 |
[33] |
Rohand, T.; Baruah, M.; Qin, W.; Boens, N.; Dehaen, W. Chem. Commun. 2006, 266.
|
[34] |
Niu, L.-Y.; Guan, Y.-S.; Chen, Y.-Z.; Wu, L.-Z.; Tung, C.-H.; Yang, Q.-Z. J. Am. Chem. Soc. 2012, 134, 18928.
doi: 10.1021/ja309079f |
[35] |
Zou, J.; Wang, P.; Wang, Y.; Liu, G.; Zhang, Y.; Zhang, Q.; Shao, J.; Si, W.; Huang, W.; Dong, X. Chem. Sci. 2019, 10, 268.
doi: 10.1039/C8SC02443J |
[36] |
Ye, S.; Rao, J.; Qiu, S.; Zhao, J.; He, H.; Yan, Z.; Yang, T.; Deng, Y.; Ke, H.; Yang, H.; Zhao, Y.; Guo, Z.; Chen, H. Adv. Mater. 2018, 30, 1801216.
doi: 10.1002/adma.201801216 |
[37] |
Zhang, X.; Zhang, Y.; Chen, L.; Xiao, Y. RSC Adv. 2015, 5, 32283.
doi: 10.1039/C5RA02414E |
[38] |
Zhu, S.; Zhang, J.; Vegesna, G.; Tiwari, A.; Luo, F.-T.; Zeller, M.; Luck, R.; Li, H.; Green, S.; Liu, H. RSC Adv. 2012, 2, 404.
doi: 10.1039/C1RA00678A |
[39] |
Mula, S.; Ulrich, G.; Ziessel, R. Tetrahedron Lett. 2009, 50, 6383.
doi: 10.1016/j.tetlet.2009.08.091 |
[40] |
Kölmel, D. K.; Barandun, L. J.; Kool, E. T. Org. Biomol. Chem. 2016, 14, 6407.
doi: 10.1039/C6OB01199C |
[41] |
Obondi, C. O.; Lim, G. N.; Karr, P. A.; Nesterov, V. N.; D'Souza, F. Phys. Chem. Chem. Phys. 2016, 18, 18187.
doi: 10.1039/C6CP03479A |
[42] |
Ziessel, R.; Ulrich, G.; Harriman, A.; Alamiry, M. A. H.; Stewart, B.; Retailleau, P. Chem.-Eur. J. 2009, 15, 1359.
doi: 10.1002/chem.200801911 |
[43] |
Ansteatt, S.; Meares, A.; Ptaszek, M. J. Org. Chem. 2021, 86, 8755.
doi: 10.1021/acs.joc.1c00586 |
[44] |
Zhang, D.; Xu, N.; Xian, L.; Ge, H.; Fan, J.; Du, J.; Peng, X. Chin. J. Chem. 2018, 36, 119.
doi: 10.1002/cjoc.201700598 |
[45] |
Gomez-Duran, C. F. A.; Hu, R.; Feng, G.; Li, T.; Bu, F.; Arseneault, M.; Liu, B.; Peña-Cabrera, E.; Tang, B. Z. ACS Appl. Mater. Interfaces 2015, 7, 15168.
doi: 10.1021/acsami.5b05033 |
[46] |
Yin, J.-F.; Hu, Y.; Wang, H.; Jin, Z.; Zhang, Y.; Kuang, G.-C. Chem. - Asian J. 2017, 12, 3088.
doi: 10.1002/asia.201701323 |
[47] |
Wang, R.; Gu, X.; Li, Q.; Gao, J.; Shi, B.; Xu, G.; Zhu, T.; Tian, H.; Zhao, C. J. Am. Chem. Soc. 2020, 142, 15084.
doi: 10.1021/jacs.0c06533 |
[48] |
Wang, L. F.; Qian, Y. Chin. J. Org. Chem. 2020, 40, 1246. (in Chinese)
doi: 10.6023/cjoc201911022 |
(王凌锋, 钱鹰, 有机化学, 2020, 40, 1246.)
doi: 10.6023/cjoc201911022 |
|
[49] |
Pereira, N.; Serra, A. C.; Pineiro, M.; Rocha -Gonsalves, A. M. d. A.; Abrantes, M.; Laranjo, M.; Botelho, F. J. Porphyrins Phthalocyanines 2010, 14, 438.
doi: 10.1142/S1088424610002227 |
[50] |
Ramos-Torres, A.; Avellanal-Zaballa, E.; Prieto-Castaneda, A.; Garcia-Garrido, F.; Banuelos, J.; Agarrabeitia, A. R.; Ortiz, M. J. Org. Lett. 2019, 21, 4563.
doi: 10.1021/acs.orglett.9b01465 pmid: 31179708 |
[51] |
Lv, F.; Yu, Y.; Hao, E.; Yu, C.; Wang, H.; Boens, N.; Jiao, L. Org. Biomol. Chem. 2019, 17, 5121.
doi: 10.1039/C9OB00927B |
[52] |
Ali, H.; Guerin, B.; van Lier, J. E. Dyes Pigm. 2020, 179, 108399.
doi: 10.1016/j.dyepig.2020.108399 |
[53] |
Lee, J.-J.; Lee, S.-C.; Zhai, D.; Ahn, Y.-H.; Yeo, H. Y.; Tan, Y. L.; Chang, Y.-T. Chem. Commun. 2011, 47, 4508.
doi: 10.1039/c1cc10362h |
[54] |
Sritharan, S. R.; Hussein, B. A.; Machin, D. D.; El-Aooiti, M. A.; Adjei, J. A.; Singh, J. K.; Pau, J. T. H.; Dhindsa, J. S.; Lough, A. J.; Koivisto, B. D. RSC Adv. 2017, 7, 8922.
doi: 10.1039/C6RA28114A |
[55] |
Zhang, Y.; Zhang, J.; Su, M.; Li, C. Biosens. Bioelectron. 2021, 175, 112866.
doi: 10.1016/j.bios.2020.112866 |
[56] |
Verbelen, B.; Cunha Dias Rezende, L.; Boodts, S.; Jacobs, J.; Van Meervelt, L.; Hofkens, J.; Dehaen, W. Chem.-Eur. J. 2015, 21, 12667.
doi: 10.1002/chem.201500938 pmid: 26215785 |
[57] |
Verbelen, B.; Boodts, S.; Hofkens, J.; Boens, N.; Dehaen, W. Angew. Chem., Int. Ed. 2015, 54, 4612.
doi: 10.1002/anie.201410853 |
[58] |
Wang, D.; Cheng, C.; Wu, Q.; Wang, J.; Kang, Z.; Guo, X.; Wu, H.; Hao, E.; Jiao, L. Org. Lett. 2019, 21, 5121.
doi: 10.1021/acs.orglett.9b01722 |
[59] |
Lv, F.; Yu, Y.; Hao, E.; Yu, C.; Wang, H.; Jiao, L.; Boens, N. Chem. Commun. 2018, 54, 9059.
doi: 10.1039/C8CC04679D |
[60] |
Wang, D.; Wu, Q.; Zhang, X.; Wang, W.; Hao, E.; Jiao, L. Org. Lett. 2020, 22, 7694.
doi: 10.1021/acs.orglett.0c02895 |
[61] |
Su, G.; Zhang, K.; Sha, F.; Tong, Z.; Ni, J.; Li, C.; Li, Q.; Du, Y.; Cao, X.; Wu, X.-Y.; Xie, Y. Dyes Pigm. 2020, 180, 108504.
doi: 10.1016/j.dyepig.2020.108504 |
[62] |
Wang, D.; Guo, X.; Wu, H.; Wu, Q.; Wang, H.; Zhang, X.; Hao, E.; Jiao, L. J. Org. Chem. 2020, 85, 8360.
doi: 10.1021/acs.joc.0c00620 |
[63] |
Zhang, H.; Chen, X.; Lan, J.; Liu, Y.; Zhou, F.; Wu, D.; You, J. Chem. Commun. 2018, 54, 3219.
doi: 10.1039/C8CC00238J |
[64] |
Lv, F.; Tang, B.; Hao, E.; Liu, Q.; Wang, H.; Jiao, L. Chem. Commun. 2019, 55, 1639.
doi: 10.1039/C8CC09821B |
[65] |
Ma, F.; Zhou, L.; Liu, Q.; Li, C.; Xie, Y. Org. Lett. 2019, 21, 733.
doi: 10.1021/acs.orglett.8b03954 |
[66] |
Li, H.; Lv, F.; Guo, X.; Wu, Q.; Wu, H.; Tang, B.; Yu, C.; Wang, H.; Jiao, L.; Hao, E. Chem. Commun. 2021, 57, 1647.
doi: 10.1039/D0CC07961H |
[67] |
Hayashi, Y.; Yamaguchi, S.; Cha, W. Y.; Kim, D.; Shinokubo, H. Org. Lett. 2011, 13, 2992.
doi: 10.1021/ol200799u pmid: 21591621 |
[68] |
Jiao, L.; Pang, W.; Zhou, J.; Wei, Y.; Mu, X.; Bai, G.; Hao, E. J. Org. Chem. 2011, 76, 9988.
doi: 10.1021/jo201754m |
[69] |
Ortiz, M. J.; Agarrabeitia, A. R.; Duran-Sampedro, G.; Bañuelos Prieto, J.; Lopez, T. A.; Massad, W. A.; Montejano, H. A.; García, N. A.; Lopez Arbeloa, I. Tetrahedron 2012, 68, 1153.
doi: 10.1016/j.tet.2011.11.070 |
[70] |
Yogo, T.; Urano, Y.; Ishitsuka, Y.; Maniwa, F.; Nagano, T. J. Am. Chem. Soc. 2005, 127, 12162.
doi: 10.1021/ja0528533 |
[71] |
Chen, Y.; Zhao, J.; Xie, L.; Guo, H.; Li, Q. RSC Adv. 2012, 2, 3942.
doi: 10.1039/c2ra01064j |
[72] |
Jiao, L.; Yu, C.; Li, J.; Wang, Z.; Wu, M.; Hao, E. J. Org. Chem. 2009, 74, 7525.
doi: 10.1021/jo901407h |
[73] |
Mirri, G.; Schoenmakers, D. C.; Kouwer, P. H. J.; Veranič, P.; Muševič, I.; Štefane, B. ChemistryOpen 2016, 5, 450.
doi: 10.1002/open.201600067 |
[74] |
Zhu, S.; Bi, J.; Vegesna, G.; Zhang, J.; Luo, F.-T.; Valenzano, L.; Liu, H. RSC Adv. 2013, 3, 4793.
doi: 10.1039/c3ra22610g |
[75] |
Cheng, H.-r.; Qian, Y. RSC Adv. 2015, 5, 82887.
doi: 10.1039/C5RA15546K |
[76] |
Cakmak, Y.; Kolemen, S.; Duman, S.; Dede, Y.; Dolen, Y.; Kilic, B.; Kostereli, Z.; Yildirim, L. T.; Dogan, A. L.; Guc, D.; Akkaya, E. U. Angew. Chem., Int. Ed. 2011, 50, 11937.
doi: 10.1002/anie.201105736 |
[77] |
Li, L.; Han, J.; Nguyen, B.; Burgess, K. J. Org. Chem. 2008, 73, 1963.
doi: 10.1021/jo702463f |
[78] |
Gupta, M.; Mula, S.; Tyagi, M.; Ghanty, T. K.; Murudkar, S.; Ray, A. K.; Chattopadhyay, S. Chem.-Eur. J. 2013, 19, 17766.
doi: 10.1002/chem.201302359 |
[79] |
Ou, Q.; Peng, Q.; Shuai, Z. J. Phys. Chem. Lett. 2020, 11, 7790.
doi: 10.1021/acs.jpclett.0c02054 |
[80] |
de Rezende, L. C. D.; de Melo, S. M. G.; Boodts, S.; Verbelen, B.; Dehaen, W.; da Silva Emery, F. Org. Biomol. Chem. 2015, 13, 6031.
doi: 10.1039/c5ob00499c pmid: 25946645 |
[81] |
Luo, L.; Wu, D.; Li, W.; Zhang, S.; Ma, Y.; Yan, S.; You, J. Org. Lett. 2014, 16, 6080.
doi: 10.1021/ol502883x |
[82] |
Leen, V.; Miscoria, D.; Yin, S.; Filarowski, A.; Molisho Ngongo, J.; Van der Auweraer, M.; Boens, N.; Dehaen, W. J. Org. Chem. 2011, 76, 8168.
doi: 10.1021/jo201082z |
[83] |
Leen, V.; Yuan, P.; Wang, L.; Boens, N.; Dehaen, W. Org. Lett. 2012, 14, 6150.
doi: 10.1021/ol3028225 |
[84] |
Liu, Y.; Lv, X.; Hou, M.; Shi, Y.; Guo, W. Anal. Chem. 2015, 87, 11475.
doi: 10.1021/acs.analchem.5b03286 |
[85] |
Goud, T. V.; Tutar, A.; Biellmann, J.-F. Tetrahedron 2006, 62, 5084.
doi: 10.1016/j.tet.2006.03.036 |
[86] |
Esnal, I.; Urías-Benavides, A.; Gómez-Durán, C. F. A.; Osorio-Martínez, C. A.; García-Moreno, I.; Costela, A.; Bañuelos, J.; Epelde, N.; López Arbeloa, I.; Hu, R.; Zhong Tang, B.; Peña-Cabrera, E. Chem.-Asian J. 2013, 8, 2691.
doi: 10.1002/asia.201300760 |
[87] |
Roacho, R. I.; Metta-Magaña, A.; Peña-Cabrera, E.; Pannell, K. Org. Biomol. Chem. 2015, 13, 995.
doi: 10.1039/C4OB01892C |
[88] |
Flores-Rizo, J. O.; Esnal, I.; Osorio-Martı́nez, C. A.; Gómez-Durán, C. F. A.; Bañuelos, J.; López Arbeloa, I.; Pannell, K. H.; Metta-Magaña, A. J.; Peña-Cabrera, E. J. Org. Chem. 2013, 78, 5867.
doi: 10.1021/jo400417h pmid: 23721096 |
[89] |
Gutiérrez-Ramos, B. D.; Bañuelos, J.; Arbeloa, T.; Arbeloa, I. L.; González-Navarro, P. E.; Wrobel, K.; Cerdán, L.; García-Moreno, I.; Costela, A.; Peña-Cabrera, E. Chem.-Eur. J. 2015, 21, 1755.
doi: 10.1002/chem.201405233 pmid: 25470456 |
[90] |
Esnal, I.; Valois-Escamilla, I.; Gómez-Durán, C. F. A.; Urías-Benavides, A.; Betancourt-Mendiola, M. L.; López-Arbeloa, I.; Bañuelos, J.; García-Moreno, I.; Costela, A.; Peña-Cabrera, E. ChemPhysChem 2013, 14, 4134.
doi: 10.1002/cphc.201300818 |
[91] |
Gao, J.; Tao, Y.; Zhang, J.; Wang, N.; Ji, X.; He, J.; Si, Y.; Zhao, W. Chem.-Eur. J. 2019, 25, 11246.
|
[92] |
Ji, X.; Lv, M.; Pan, F.; Zhang, J.; Wang, J.; Wang, J.; Zhao, W. Spectrochim. Acta, Part A 2019, 206, 1.
|
[93] |
Ji, X.; Wang, N.; Zhang, J.; Xu, S.; Si, Y.; Zhao, W. Dyes Pigm. 2021, 187, 109089.
doi: 10.1016/j.dyepig.2020.109089 |
[94] |
Peña-Cabrera, E.; Aguilar-Aguilar, A.; González-Domínguez, M.; Lager, E.; Zamudio-Vázquez, R.; Godoy-Vargas, J.; Villanueva-García, F. Org. Lett. 2007, 9, 3985.
pmid: 17764191 |
[95] |
Betancourt-Mendiola, L.; Valois-Escamilla, I.; Arbeloa, T.; Bañuelos, J.; López Arbeloa, I.; Flores-Rizo, J. O.; Hu, R.; Lager, E.; Gómez-Durán, C. F. A.; Belmonte-Vázquez, J. L.; Martínez- González, M. R.; Arroyo, I. J.; Osorio-Martínez, C. A.; Alvarado- Martínez, E.; Urías-Benavides, A.; Gutiérrez-Ramos, B. D.; Tang, B. Z.; Peña-Cabrera, E. J. Org. Chem. 2015, 80, 5771.
doi: 10.1021/acs.joc.5b00731 pmid: 25965325 |
[96] |
Ulrich, G.; Goze, C.; Guardigli, M.; Roda, A.; Ziessel, R. Angew. Chem., Int. Ed. 2005, 44, 3694.
doi: 10.1002/anie.200500808 |
[97] |
Goze, C.; Ulrich, G.; Ziessel, R. Org. Lett. 2006, 8, 4445.
doi: 10.1021/ol061601j |
[98] |
Goze, C.; Ulrich, G.; Ziessel, R. J. Org. Chem. 2007, 72, 313.
doi: 10.1021/jo060984w |
[99] |
Ulrich, G.; Goze, C.; Goeb, S.; Retailleau, P.; Ziessel, R. New J. Chem. 2006, 30, 982.
doi: 10.1039/b604830g |
[100] |
Goze, C.; Ulrich, G.; Mallon, L. J.; Allen, B. D.; Harriman, A.; Ziessel, R. J. Am. Chem. Soc. 2006, 128, 10231.
doi: 10.1021/ja062405a |
[101] |
More, A. B.; Mula, S.; Thakare, S.; Sekar, N.; Ray, A. K.; Chattopadhyay, S. J. Org. Chem. 2014, 79, 10981.
doi: 10.1021/jo502028g |
[102] |
Tahtaoui, C.; Thomas, C.; Rohmer, F.; Klotz, P.; Duportail, G.; Mély, Y.; Bonnet, D.; Hibert, M. J. Org. Chem. 2007, 72, 269.
pmid: 17194109 |
[103] |
Liu, Y.; Niu, L.-Y.; Liu, X.-L.; Chen, P.-Z.; Yao, Y.-S.; Chen, Y.-Z.; Yang, Q.-Z. Chem.-Eur. J. 2018, 24, 13549.
doi: 10.1002/chem.201802157 pmid: 29952087 |
[104] |
Alnoman, R. B.; Rihn, S.; O'Connor, D. C.; Black, F. A.; Costello, B.; Waddell, P. G.; Clegg, W.; Peacock, R. D.; Herrebout, W.; Knight, J. G.; Hall, M. J. Chem.-Eur. J. 2016, 22, 93.
doi: 10.1002/chem.201504484 pmid: 26555772 |
[105] |
Lundrigan, T.; Crawford, S. M.; Cameron, T. S.; Thompson, A. Chem. Commun. 2012, 48, 1003.
doi: 10.1039/C1CC16351E |
[106] |
Lundrigan, T.; Thompson, A. J. Org. Chem. 2013, 78, 757.
doi: 10.1021/jo302277d pmid: 23237433 |
[107] |
Teng, K.-X.; Chen, W.-K.; Niu, L.-Y.; Fang, W.-H.; Cui, G.; Yang, Q.-Z. Angew. Chem., Int. Ed. 2021, 60, 19912.
doi: 10.1002/anie.202106748 |
[108] |
Zhou, Z.; Zhou, J.; Gai, L.; Yuan, A.; Shen, Z. Chem. Commun. 2017, 53, 6621.
doi: 10.1039/C7CC02918G |
[109] |
Wang, Z.; Huang, L.; Yan, Y.; El-Zohry, A. M.; Toffoletti, A.; Zhao, J.; Barbon, A.; Dick, B.; Mohammed, O. F.; Han, G. Angew. Chem., Int. Ed. 2020, 59, 16114.
doi: 10.1002/anie.202005269 |
[110] |
Zhang, W.; Sheng, W.; Yu, C.; Wei, Y.; Wang, H.; Hao, E.; Jiao, L. Chem. Commun. 2017, 53, 5318.
doi: 10.1039/C7CC02393F |
[111] |
Xu, Y.; Chang, D.; Feng, S.; Zhang, C.; Jiang, J.-X. New J. Chem. 2016, 40, 9415.
doi: 10.1039/C6NJ01812B |
[112] |
Teng, K.-X.; Niu, L.-Y.; Li, J.; Jia, L.; Yang, Q.-Z. Chem. Commun. 2019, 55, 13761.
doi: 10.1039/C9CC07730H |
[113] |
Wang, H.; Fronczek, F. R.; Vicente, M. G. H.; Smith, K. M. J. Org. Chem. 2014, 79, 10342.
doi: 10.1021/jo501969z |
[114] |
Wu, Q.; Kang, Z.; Gong, Q.; Guo, X.; Wang, H.; Wang, D.; Jiao, L.; Hao, E. Org. Lett. 2020, 22, 7513.
doi: 10.1021/acs.orglett.0c02704 |
[115] |
Duran-Sampedro, G.; Palao, E.; Agarrabeitia, A. R.; Moya, S. d. l.; Boens, N.; Ortiz, M. J. RSC Adv. 2014, 4, 19210.
doi: 10.1039/C4RA00651H |
[116] |
Gai, L.; Mack, J.; Lu, H.; Yamada, H.; Kuzuhara, D.; Lai, G.; Li, Z.; Shen, Z. Chem.-Eur. J. 2014, 20, 1091.
doi: 10.1002/chem.201303291 |
[117] |
Lu, H.; Mack, J.; Yang, Y.; Shen, Z. Chem. Soc. Rev. 2014, 43, 4778.
doi: 10.1039/C4CS00030G |
[118] |
Li, K.; Duan, X.; Jiang, Z.; Ding, D.; Chen, Y.; Zhang, G.-Q.; Liu, Z. Nat. Commun. 2021, 12, 2376.
doi: 10.1038/s41467-021-22686-z |
[119] |
Hayashi, Y.; Obata, N.; Tamaru, M.; Yamaguchi, S.; Matsuo, Y.; Saeki, A.; Seki, S.; Kureishi, Y.; Saito, S.; Yamaguchi, S.; Shinokubo, H. Org. Lett. 2012, 14, 866.
doi: 10.1021/ol2033916 pmid: 22273338 |
[120] |
Ito, H.; Sakai, H.; Suzuki, Y.; Kawamata, J.; Hasobe, T. Chem.-Eur. J. 2020, 26, 316.
doi: 10.1002/chem.201904282 |
[121] |
Gobo, Y.; Matsuoka, R.; Chiba, Y.; Nakamura, T.; Nabeshima, T. Tetrahedron Lett. 2018, 59, 4149.
doi: 10.1016/j.tetlet.2018.10.003 |
[122] |
Miao, W.; Feng, Y.; Wu, Q.; Sheng, W.; Li, M.; Liu, Q.; Hao, E.; Jiao, L. J. Org. Chem. 2019, 84, 9693.
doi: 10.1021/acs.joc.9b01425 pmid: 31287311 |
[123] |
Patra, A.; Patalag, L. J.; Jones, P. G.; Werz, D. B. Angew. Chem., Int. Ed. 2021, 60, 747.
doi: 10.1002/anie.202012335 |
[124] |
Yokoi, H.; Wachi, N.; Hiroto, S.; Shinokubo, H. Chem. Commun. 2014, 50, 2715.
doi: 10.1039/C3CC48738E |
[125] |
Yang, X.; Jiang, L.; Yang, M.; Zhang, H.; Lan, J.; Zhou, F.; Chen, X.; Wu, D.; You, J. J. Org. Chem. 2018, 83, 9538.
doi: 10.1021/acs.joc.8b01239 |
[126] |
Labella, J.; Durán-Sampedro, G.; Martínez-Díaz, M. V.; Torres, T. Chem. Sci. 2020, 11, 10778.
doi: 10.1039/d0sc01054e pmid: 34094331 |
[127] |
Zhou, B.; Guo, M.; Pan, Q.; Zhou, M.; Xu, L.; Rao, Y.; Wang, K.; Yin, B.; Zhou, J.; Song, J. Org. Chem. Front. 2021, 8, 868.
doi: 10.1039/D0QO01625J |
[128] |
Fan, G.; Yang, L.; Chen, Z. Front. Chem. Sci. Eng. 2014, 8, 405.
doi: 10.1007/s11705-014-1445-7 |
[129] |
Zhao, X. L.; Li, N.; Liu, F. Y.; Gao, C.; Feng, J. B.; Liu, L. P.; Guan, X. L.; Yan, N. Chin. J. Org. Chem. 2020, 40, 4339. (in Chinese)
doi: 10.6023/cjoc202007022 |
(赵小龙, 李娜, 刘发玉, 高超, 丰久彪, 刘乐平, 关晓琳, 燕娜, 有机化学, 2020, 40, 4339.)
doi: 10.6023/cjoc202007022 |
|
[130] |
Morgan, L. R.; Boyer, J. H. US 5446157, 1995[Chem. Abstr. 1994, 2156508]
|
[131] |
Zhang, H.; Liu, J.; Sun, Y.-Q.; Liu, M.; Guo, W. J. Am. Chem. Soc. 2020, 142, 17069.
doi: 10.1021/jacs.0c06916 |
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