Chem. J. Chinese Universities ›› 2020, Vol. 41 ›› Issue (7): 1407.doi: 10.7503/cjcu20200205
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ZHU Min1,2,ZHANG Xiao1,YOU Shuli1,2,*()
Received:
2020-04-14
Online:
2020-07-10
Published:
2020-06-10
Contact:
Shuli YOU
E-mail:slyou@sioc.ac.cn
Supported by:
CLC Number:
TrendMD:
ZHU Min, ZHANG Xiao, YOU Shuli. Visible-light-promoted Dearomatization of Benzene and Derivatives†[J]. Chem. J. Chinese Universities, 2020, 41(7): 1407.
[1] |
Pape A. R., Kaliappan K. P., Kündig E. P., Chem. Rev., 2000, 100, 2917—2940
doi: 10.1021/cr9902852 URL pmid: 11749310 |
[2] |
Zhuo C. X., Zhang W., You S. L., Angew. Chem. Int. Ed., 2012, 51, 12662—12686
doi: 10.1002/anie.201204822 URL |
[3] |
Zhuo C. X., Zheng C., You S. L., Acc. Chem. Res., 2014, 47, 2558—2573
doi: 10.1021/ar500167f URL pmid: 24940612 |
[4] |
Duan D. H., Yin Q., Wang S. G., Gu Q., You S. L., Acta Chim. Sinica, 2014, 72, 1001—1004
doi: 10.6023/A14060497 URL |
( 段德河, 殷勤, 王守国, 顾庆, 游书力. 化学学报, 2014, 72, 1001—1004)
doi: 10.6023/A14060497 URL |
|
[5] |
Wu W. T., Zhang L., You S. L., Chem. Soc. Rev., 2016, 45, 1570—1580
doi: 10.1039/c5cs00356c URL pmid: 26796922 |
[6] |
Zheng C., You S. L., Chem., 2016, 1, 830—857
doi: 10.1016/j.chempr.2016.11.005 URL |
[7] |
Wu W. T., Zhang L. M You S. L., Acta Chim. Sinica, 2017, 75, 419
doi: 10.6023/A17020049 URL |
( 吴文挺, 张立明, 游书力. 化学学报, 2017, 75, 419—438)
doi: 10.6023/A17020049 URL |
|
[8] |
Southgate E. H., Holycross D. R., Sarlah D., Angew. Chem. Int. Ed., 2017, 56, 15049—15052
doi: 10.1002/anie.201709712 URL |
[9] |
Hernandez L. W., Pospech J., Klöeckner U., Bingham T. W., Sarlah D., J. Am. Chem. Soc., 2017, 139, 15656—15659
doi: 10.1021/jacs.7b10351 URL pmid: 29059521 |
[10] |
Dennis D. G., Okumura M., Sarlah D., J. Am. Chem. Soc., 2019, 141, 10193—10198
URL pmid: 31244190 |
[11] |
Bingham T. W., Hernandez L. W., Olson D. G., Svec R. L., Hergenrother P. J., Sarlah D., J. Am. Chem. Soc., 2019, 141, 657—670
URL pmid: 30520639 |
[12] |
Zheng C., You S. L., Nat. Prod. Rep., 2019, 36, 1589—1605
URL pmid: 30839047 |
[13] |
Boyd D. R., Bugg T. D. H., Org. Biomol. Chem., 2006, 4, 181—192
doi: 10.1039/b513226f URL pmid: 16391757 |
[14] |
Rosillo M., Domınguez G., Perez-Castells J., Chem. Soc. Rev., 2007, 36, 1589—1604
URL pmid: 17721584 |
[15] |
Liebov B. K., Harman W. D., Chem. Rev., 2017, 117, 13721—13755
doi: 10.1021/acs.chemrev.7b00480 URL pmid: 29064228 |
[16] |
Wertjes W. C., Southgate E. H., Sarlah D., Chem. Soc. Rev., 2018, 47, 7996—8017
URL pmid: 30073226 |
[17] |
Bryce-Smith D., Gilbert A., Tetrahedron, 1976, 32, 1309—1326
doi: 10.1016/0040-4020(76)85002-8 URL |
[18] | Bryce-Smith D., Gilbert A., Tetrahedron, 1977, 33, 2459—2489 |
[19] | McCullough J. J., Chem. Rev., 1987, 87, 811—860 |
[20] |
Remy R., Bochet C. G., Chem. Rev., 2016, 116, 9816—9849
URL pmid: 27340900 |
[21] | Okumura M., Sarlah D., Eur. J. Org. Chem., 2020, 2020, 1259—1273 |
[22] |
Dong W., Yuan Y., Xie X., Zhang Z. G., Org. Lett., 2020, 22, 528—532
URL pmid: 31908167 |
[23] |
Dai W., Geib S. J., Curran D. P., J. Am. Chem. Soc., 2020, 142, 6261—6267
URL pmid: 32101418 |
[24] |
Guo Y., Nguyen T. V., Koenigs R. M., Org. Lett., 2019, 21, 8814—8818
URL pmid: 31617724 |
[25] | Hamrock S. J., Sheridan R. S., J. Am. Chem. Soc., 1989, 111, 9247—9249 |
[26] |
Southgate E. H., Pospech J., Fu J., Holycross D. R., Sarlah D., Nat. Chem., 2016, 8, 922—928
URL pmid: 27657867 |
[27] |
Hernandez L. W., Klöckner U., Pospech J., Hauss L., Sarlah D., J. Am. Chem. Soc., 2018, 140, 4503—4507
URL pmid: 29544244 |
[28] |
James M. J., Schwarz J. L., Strieth-Kalthoff F., Wibbeling B., Glorius F., J. Am. Chem. Soc., 2018, 140, 8624—8628
doi: 10.1021/jacs.8b03302 URL |
[29] |
Zhu M., Zheng C., Zhang X., You S. L., J. Am. Chem. Soc., 2019, 141, 2636—2644
URL pmid: 30653315 |
[30] |
Cheng Y. Z., Zhao Q. R., Zhang X., You S. L., Angew. Chem. Int. Ed., 2019, 58, 18069—18074
doi: 10.1002/anie.v58.50 URL |
[31] | Zhu M., Huang X. L., Xu H., Zheng C., Zhang X., You S. L., CCS Chem., 2020, 2, 652—664 |
[32] | Ma J., Strieth-Kalthoff F., Dalton T., Freitag M., Schwarz J. L., Bergander K., Daniliuc C., Glorius F., Chem., 2019, 5, 2854—2864 |
[33] |
Soni V. K., Hwang H. S., Moon Y. K., Park S. W., You Y., Cho E. J., J. Am. Chem. Soc., 2019, 141, 10538—10545
URL pmid: 31244191 |
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