Ag-catalyzed sulfonylation-peroxidation of alkenes with sulfonyl hydrazides and T-hydro
Tài liệu tham khảo
Lan, 2017, Eur. J. Org. Chem., 5821, 10.1002/ejoc.201700678
Yi, 2017, Chem. Rev., 117, 9016, 10.1021/acs.chemrev.6b00620
Xuan, 2017, Chem. Soc. Rev., 46, 4329, 10.1039/C6CS00912C
Yu, 2016, Chem. Commun., 52, 2220, 10.1039/C5CC08872K
Studer, 2016, Angew. Chem. Int. Ed., 55, 58, 10.1002/anie.201505090
Clark, 2016, Eur. J. Org. Chem., 2231, 10.1002/ejoc.201501571
Kindt, 2016, Synthesis, 48, 1597, 10.1055/s-0035-1561586
Reiser, 2016, Acc. Chem. Res., 49, 1990, 10.1021/acs.accounts.6b00296
Cao, 2015, Tetrahedron Lett., 56, 3732, 10.1016/j.tetlet.2015.04.091
Egami, 2014, Angew. Chem. Int. Ed., 53, 8294, 10.1002/anie.201309260
Casteel, 1999, Nat. Prod. Rep., 16, 55, 10.1039/a705725c
Yin, 2011, Chem. Rev., 111, 5944, 10.1021/cr200084z
Posner, 2004, Acc. Chem. Res., 37, 397, 10.1021/ar020227u
Tang, 2004, Med. Res. Rev., 24, 425, 10.1002/med.10066
O'Neill, 2004, J. Med. Chem., 47, 2945, 10.1021/jm030571c
2006, Vol. 2
2000
Murahashi, 2008, Chem. Soc. Rev., 37, 1490, 10.1039/b706709g
Meier, 2011, Angew. Chem. Int. Ed., 50, 3280, 10.1002/anie.201007315
Tokuyasu, 2005, J. Org. Chem., 70, 251, 10.1021/jo048359j
Reeves, 2003, Chem. Rev., 103, 5199, 10.1021/cr0205053
Kharasch, 1953, J. Org. Chem., 18, 322, 10.1021/jo01131a016
Kharasch, 1958, J. Org. Chem., 23, 324
Kharasch, 1959, J. Org. Chem., 24, 72, 10.1021/jo01083a022
Sevin, 2001, J. Am. Chem. Soc., 123, 4591, 10.1021/ja010138x
Foote, 1995
Lissi, 1993, Chem. Rev., 93, 699, 10.1021/cr00018a004
Kearns, 1971, Chem. Rev., 71, 395, 10.1021/cr60272a004
Spantulescu, 2009, Org. Lett., 11, 645, 10.1021/ol802745n
Hou, 2009, J. Org. Chem., 74, 6362, 10.1021/jo901086s
Dai, 2005, Org. Lett., 7, 4333, 10.1021/ol051407h
Dussault, 2000, J. Chem. Soc., Perkin Trans. 1, 3006, 10.1039/b001391i
Liu, 2011, J. Am. Chem. Soc., 133, 10756, 10.1021/ja204226n
Lv, 2017, J. Org. Chem., 82, 5487, 10.1021/acs.joc.7b00693
Lv, 2014, Angew. Chem. Int. Ed., 53, 4164, 10.1002/anie.201400326
Gandhi, 2017, RSC Adv., 7, 19506, 10.1039/C6RA28489B
Zhao, 2017, Inorg. Chem., 56, 8166, 10.1021/acs.inorgchem.7b00888
Yang, 2015, Org. Biomol. Chem., 13, 2385, 10.1039/C4OB02621G
Liu, 2012, Tetrahedron, 68, 10333, 10.1016/j.tet.2012.09.110
Cheng, 2017, Chem. Commun., 53, 12830, 10.1039/C7CC08074C
Zong, 2015, Tetrahedron Lett., 56, 6719, 10.1016/j.tetlet.2015.10.052
Lu, 2017, Org. Chem., 6, 313
Lan, 2017, Org. Chem. Front., 4, 1411, 10.1039/C7QO00149E
Cheng, 2015, J. Am. Chem. Soc., 137, 42, 10.1021/ja510635k
Banerjee, 2015, Chem. Commun., 51, 15422, 10.1039/C5CC06200D
Jiang, 2015, Chem. Commun., 51, 14728, 10.1039/C5CC05183E
Banerjee, 2015, Org. Biomol. Chem., 13, 1307, 10.1039/C4OB01962H
Schweitzer-Chaput, 2014, Angew. Chem. Int. Ed., 53, 8737, 10.1002/anie.201401062
Zhang, 2017, Org. Lett., 19, 5260, 10.1021/acs.orglett.7b02353
Shi, 2016, J. Org. Chem., 81, 5878, 10.1021/acs.joc.6b00575
Chen, 2018, Org. Chem. Front., 5, 972, 10.1039/C7QO01045A
Wang, 2017, Beilstein J. Org. Chem., 13, 2023, 10.3762/bjoc.13.200
Terent’ev, 2015, Org. Biomol. Chem., 13, 1439, 10.1039/C4OB01823K
Lu, 2018, Tetrahedron Lett., 59, 2604, 10.1016/j.tetlet.2018.05.072
Lan, 2017, ACS Catal., 7, 7120, 10.1021/acscatal.7b02754
Ivachtchenko, 2011, J. Med. Chem., 54, 8161, 10.1021/jm201079g
Huang, 2011, Chem. Commun., 47, 8904, 10.1039/c1cc12575c
Whitham, 1995
Simpkins, 1993
He, 2018, Org. Chem. Front., 5, 2437, 10.1039/C8QO00528A
Zhang, 2017, Chem. Eur. J., 23, 9477, 10.1002/chem.201702190
Choudhuri, 2017, Adv. Synth. Catal., 359, 3566, 10.1002/adsc.201700772
Wang, 2017, Chem. Commun., 53, 2056, 10.1039/C7CC00090A
Wan, 2017, Sci. China Chem., 60, 353, 10.1007/s11426-016-0284-2
Liu, 2016, Eur. J. Org. Chem., 910, 10.1002/ejoc.201501613
Yang, 2016, Green. Chem., 18, 5630, 10.1039/C6GC01403H
Koike, 2016, Org. Chem. Front., 3, 1345, 10.1039/C6QO00139D
Tang, 2015, Org. Biomol. Chem., 13, 7084, 10.1039/C5OB00742A
Taniguchi, 2015, J. Org. Chem., 80, 7797, 10.1021/acs.joc.5b01176
Singh, 2014, Org. Biomol. Chem., 12, 8550, 10.1039/C4OB00776J
Wei, 2013, Chem. Commun., 49, 10239, 10.1039/c3cc45803b
Lu, 2013, Angew. Chem. Int. Ed., 52, 7156, 10.1002/anie.201301634
Xi, 2004, Synlett, 1595, 10.1055/s-2004-829090
Chen, 2018, Chem. Rec., 18, 1, 10.1002/tcr.201880101
Qiu, 2018, Org. Chem. Front., 5, 691, 10.1039/C7QO01073G
Hofman, 2018, Chem. Eur. J., 24
Glass, 2018, Top. Curr. Chem. (Z), 376, 22, 10.1007/s41061-018-0197-0
Zhu, 2018, Adv. Synth. Catal., 360, 386, 10.1002/adsc.201701194
Yang, 2017, Tetrahedron Lett., 58, 487, 10.1016/j.tetlet.2016.12.058
Zong, 2016, Tetrahedron Lett., 57, 3827, 10.1016/j.tetlet.2016.07.034
Liu, 2013, Chem. Asian J., 8, 359, 10.1002/asia.201200973