Alper, 2001, Alkaloids: Chem. Biol., 56, 1
Popik, 1995, Pharmacol. Rev., 47, 235
Terada, 2014, J. Nat. Prod., 77, 1831, 10.1021/np500235b
Sears, 2015, Acc. Chem. Res., 48, 653, 10.1021/ar500400w
Zhang, 2016, Chem. Sci., 7, 5530, 10.1039/C6SC00932H
Faisal, 2017, Tetrahedron: Asymmetry, 28, 1445, 10.1016/j.tetasy.2017.10.013
C. Lavaud and G.Massiot , in Progress in the Chemistry of Organic Natural Products , ed. A. D. Kinghorn , H. Falk , S. Gibbons and J. Kobayashi , Springer , Switzerland , 2017 , vol. 105 , p. 89
Jana, 2011, Org. Prep. Proced. Int., 43, 541, 10.1080/00304948.2011.629563
Jana, 2012, Tetrahedron, 68, 7155, 10.1016/j.tet.2012.06.027
Kruegel, 2015, J. Org. Chem., 80, 2062, 10.1021/jo5018102
Zhao, 2016, Org. Lett., 18, 2447, 10.1021/acs.orglett.6b00989
Höck, 2004, Tetrahedron: Asymmetry, 15, 1801, 10.1016/j.tetasy.2004.04.028
Höck, 2006, Helv. Chim. Acta, 89, 542, 10.1002/hlca.200690058
Achenbach, 1980, Phytochemistry, 19, 2185, 10.1016/S0031-9422(00)82220-7
Zhang, 2015, J. Nat. Prod., 78, 1253, 10.1021/acs.jnatprod.5b00051
Nge, 2016, J. Nat. Prod., 79, 1388, 10.1021/acs.jnatprod.6b00129
Nge, 2016, J. Nat. Prod., 79, 2709, 10.1021/acs.jnatprod.6b00674
Coldham, 2007, Angew. Chem., Int. Ed., 46, 6159, 10.1002/anie.200701943
Burrell, 2009, J. Org. Chem., 74, 2290, 10.1021/jo8019913
Burrell, 2009, Org. Lett., 11, 1515, 10.1021/ol9001653
Burrell, 2010, Org. Biomol. Chem., 8, 4530, 10.1039/c0ob00408a
Coldham, 2011, J. Org. Chem., 76, 2360, 10.1021/jo2000868
Coldham, 2012, Heterocycles, 84, 597, 10.3987/COM-11-S(P)29
Coldham, 2012, Beilstein J. Org. Chem., 8, 107, 10.3762/bjoc.8.11
Coldham, 2009, Org. Biomol. Chem., 7, 1674, 10.1039/b822743h
Guerrand, 2011, Org. Biomol. Chem., 9, 7921, 10.1039/c1ob06122d
Furnival, 2016, Org. Biomol. Chem., 14, 10953, 10.1039/C6OB01871H
Coldham, 2011, Org. Lett., 13, 1267, 10.1021/ol102961x
Saruengkhanphasit, 2017, J. Org. Chem., 82, 6489, 10.1021/acs.joc.7b00959
Dondas, 2001, Tetrahedron, 57, 1119, 10.1016/S0040-4020(00)01084-X
Karatholuvhu, 2006, J. Am. Chem. Soc., 128, 12656, 10.1021/ja065015x
Yuan, 2016, Org. Lett., 18, 5500, 10.1021/acs.orglett.6b02703
Yamada, 2016, Angew. Chem., Int. Ed., 55, 6067, 10.1002/anie.201601958
Zhang, 2016, Angew. Chem., Int. Ed., 55, 11638, 10.1002/anie.201605879
Boudreault, 2016, J. Org. Chem., 81, 9247, 10.1021/acs.joc.6b01835
Hauduc, 2017, J. Org. Chem., 82, 4703, 10.1021/acs.joc.7b00345
Boissarie, 2017, Org. Lett., 19, 3739, 10.1021/acs.orglett.7b01566
Sugita, 2017, Angew. Chem., Int. Ed., 56, 2469, 10.1002/anie.201611816
Hughes, 2017, Angew. Chem., Int. Ed., 56, 10830, 10.1002/anie.201706273
Hughes, 2018, Tetrahedron, 74, 759, 10.1016/j.tet.2017.12.026
Berthold, 1957, Chem. Ber., 90, 793, 10.1002/cber.19570900526
Utimoto, 1981, Tetrahedron Lett., 22, 4279, 10.1016/S0040-4039(01)82933-6
Coldham, 2002, J. Org. Chem., 67, 6181, 10.1021/jo016376s
Pathak, 2015, Org. Biomol. Chem., 13, 3331, 10.1039/C4OB02582B
