Page 34 - Read Online

Wu et al. Chem Synth 2023;3:6 https://dx.doi.org/10.20517/cs.2022.42 Page 15 of 17

19. DOI PubMed PMC
88. Cheng JK, Xiang SH, Tan B. Organocatalytic enantioselective synthesis of axially chiral molecules: development of strategies and
skeletons. Acc Chem Res 2022;55:2920-37. DOI PubMed
89. Kumar A, Sasai H, Takizawa S. Atroposelective synthesis of C-C axially chiral compounds via mono- and dinuclear vanadium
catalysis. Acc Chem Res 2022;55:2949-65. DOI PubMed
90. Norton RS, Wells RJ. A series of chiral polybrominated biindoles from the marine blue-green alga Rivularia firma. Application of
carbon-13 NMR spin-lattice relaxation data and carbon-13-proton coupling constants to structure elucidation. J Am Chem Soc
1982;104:3628-35. DOI
91. Ito C, Thoyama Y, Omura M, Kajiura I, Furukawa H. Alkaloidal constituents of murraya koenigii. isolation and structural elucidation
of novel binary carbazolequinones and carbazole alkaloids. Chem Pharm Bull 1993;41:2096-100. DOI
92. Zhang Q, Mándi A, Li S, et al. N-N-coupled indolo-sesquiterpene atropo-diastereomers from a marine-derived actinomycete. Eur J
Org Chem 2012;2012:5256-62. DOI
93. Jiang F, Chen KW, Wu P, Zhang YC, Jiao Y, Shi F. A strategy for synthesizing axially chiral naphthyl-indoles: catalytic asymmetric
addition reactions of racemic substrates. Angew Chem Int Ed Engl 2019;58:15104-10. DOI PubMed
94. Chen KW, Chen ZH, Yang S, Wu SF, Zhang YC, Shi F. Organocatalytic atroposelective synthesis of N-N axially chiral indoles and
pyrroles by de novo ring formation. Angew Chem Int Ed Engl 2022;61:e202116829. DOI PubMed
95. Xia W, An QJ, Xiang SH, Li S, Wang YB, Tan B. Chiral phosphoric acid catalyzed atroposelective C-H amination of arenes. Angew
Chem Int Ed Engl 2020;59:6775-9. DOI PubMed
96. Baumann T, Brückner R. Atropselective dibrominations of a 1, 1'-disubstituted 2, 2'-biindolyl with diverging point-to-axial
asymmetric inductions. Deriving 2, 2'-biindolyl-3, 3'-diphosphane ligands for asymmetric catalysis. Angew Chem Int Ed Engl
2019;58:4714-9. DOI PubMed
97. He T, Peng L, Li S, et al. Chiral naphthyl-C2-indole as scaffold for phosphine organocatalysis: application in asymmetric formal
[4+2] cycloaddition reactions. Org Lett 2020;22:6966-71. DOI PubMed
98. Wang L, Zhong J, Lin X. Atroposelective phosphoric acid catalyzed three-component cascade reaction: enantioselective synthesis of
axially chiral N-arylindoles. Angew Chem Int Ed Engl 2019;58:15824-8. DOI PubMed
99. Ren Q, Cao T, He C, Yang M, Liu H, Wang L. Highly atroposelective rhodium(II)-catalyzed N-H bond insertion: access to axially
chiral N-arylindolocarbazoles. ACS Catal 2021;11:6135-40. DOI
100. Wang ZS, Zhu LJ, Li CT, Liu BY, Hong X, Ye LW. Synthesis of axially chiral N-arylindoles via atroposelective cyclization of
ynamides catalyzed by chiral Brønsted acids. Angew Chem Int Ed Engl 2022;61:e202201436. DOI PubMed
101. Yang H, Sun HR, He RQ, et al. Organocatalytic cycloaddition of alkynylindoles with azonaphthalenes for atroposelective
construction of indole-based biaryls. Nat Commun 2022;13:632. DOI PubMed PMC
102. Ototake N, Morimoto Y, Mokuya A, Fukaya H, Shida Y, Kitagawa O. Catalytic enantioselective synthesis of atropisomeric indoles
with an N-C chiral axis. Chem Eur J 2010;16:6752-5. DOI PubMed
103. Zhang J, Xu Q, Wu J, Fan J, Xie M. Construction of N-C axial chirality through atroposelective C-H olefination of N-arylindoles by
palladium/amino acid cooperative catalysis. Org Lett 2019;21:6361-5. DOI PubMed
104. Sun L, Chen H, Liu B, et al. Rhodium-catalyzed atroposelective construction of indoles via C-H bond activation. Angew Chem Int Ed
Engl 2021;60:8391-5. DOI PubMed
105. Kim A, Kim A, Park S, et al. Catalytic and enantioselective control of the C-N stereogenic axis via the Pictet-Spengler reaction.
Angew Chem Int Ed Engl 2021;60:12279-83. DOI PubMed
106. Corti V, Thøgersen MK, Enemaerke VJ, Rezayee NM, Barløse CL, Anker Jørgensen K. Construction of C-N atropisomers by
aminocatalytic enantioselective addition of indole-2-carboxaldehydes to o-quinone derivatives. Chem Eur J 2022;28:e202202395.
DOI PubMed
107. Li Y, Liou YC, Chen X, Ackermann L. Thioether-enabled palladium-catalyzed atroposelective C-H olefination for N-C and C-C
axial chirality. Chem Sci 2022;13:4088-94. DOI PubMed PMC
108. Wang Y, Zhou X, Shan W, et al. Construction of axially chiral indoles by cycloaddition-isomerization via atroposelective phosphoric
acid and silver sequential catalysis. ACS Catal 2022;12:8094-103. DOI
109. Wang P, Huang Y, Jing J, Wang F, Li X. Rhodium(III)-catalyzed atroposelective synthesis of C-N axially chiral naphthylamines and
variants via C-H activation. Org Lett 2022;24:2531-5. DOI PubMed
110. Niu C, Zhou Y, Chen Q, et al. Atroposelective synthesis of N-arylindoles via enantioselective N-H bond insertion. Org Lett
2022;24:7428-33. DOI PubMed
111. Qi LW, Mao JH, Zhang J, Tan B. Organocatalytic asymmetric arylation of indoles enabled by azo groups. Nat Chem 2018;10:58-64.
DOI PubMed
112. Bisag GD, Pecorari D, Mazzanti A, et al. Central-to-axial chirality conversion approach designed on organocatalytic enantioselective
povarov cycloadditions: first access to configurationally stable indole-quinoline atropisomers. Chem Eur J 2019;25:15694-701. DOI
PubMed
113. Mao JH, Wang YB, Yang L, et al. Organocatalyst-controlled site-selective arene C-H functionalization. Nat Chem 2021;13:982-91.
DOI PubMed
114. Xu WL, Zhao WM, Zhang RX, Chen J, Zhou L. Organocatalytic cycloaddition-elimination cascade for atroposelective construction
of heterobiaryls. Chem Sci 2021;12:14920-6. DOI PubMed PMC