Thiophene and naphthalene-based double helix: Synthesis, structures and chirality

Greviiig, 1974, Angew. Chem. Int. Ed., 13, 467, 10.1002/anie.197404672 Zhao, 2015, Chin. J. Chem., 33, 71, 10.1002/cjoc.201400524 Li, 2016, Chem. Rec., 6, 797, 10.1002/tcr.201500270 Zhao, 2019, Nat. Commun., 10, 2952, 10.1038/s41467-019-10818-5 Tian, 2018, Chem. -Eur. J., 24, 15993, 10.1002/chem.201803948 Urieta-Mora, 2019, J. Mater. Chem. C, 7, 6656, 10.1039/C9TC00437H Zhao, 2019, ACS Appl. Energy Mater., 2, 8173, 10.1021/acsaem.9b01658 Marsella, 2000, J. Am. Chem. Soc., 122, 974, 10.1021/ja9939340 Li, 2009, J. Org. Chem., 74, 408, 10.1021/jo802080g Wang, 2010, Org. Lett., 12, 456, 10.1021/ol902613g Liu, 2013, J. Org. Chem., 78, 6316, 10.1021/jo400691s Liu, 2018, Org. Chem. Front., 5, 1257, 10.1039/C7QO01049D Zhang, 2016, J. Am. Chem. Soc., 138, 10002, 10.1021/jacs.6b05709 Rajca, 1997, Angew. Chem. Int. Ed., 36, 488, 10.1002/anie.199704881 Chen, 2015, Org. Lett., 17, 4296, 10.1021/acs.orglett.5b02102 Marsella, 1999, Macromolecules, 32, 5982, 10.1021/ma990892r Sun, 2016, Polym. Chem., 7, 5031, 10.1039/C6PY00725B Marsella, 2002, J. Am. Chem. Soc., 124, 12507, 10.1021/ja0255352 Marsella, 2002, Acc. Chem. Res., 35, 944, 10.1021/ar010090s Li, 2018, Sci. China Chem., 61, 844, 10.1007/s11426-017-9233-2 Li, 2018, ACS Omega, 3, 16014, 10.1021/acsomega.8b02492