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Journal articles on the topic 'Aminoanilino'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Dorn, Angelika, Dieter Schollmeyer, and Stefan A. Laufer. "1-[4-(2-Aminoanilino)phenyl]-2,2,2-trifluoroethanone." Acta Crystallographica Section E Structure Reports Online 66, no. 5 (2010): o1149. http://dx.doi.org/10.1107/s1600536810008937.

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2

Huynh, Huy, Selçuk Çalimsiz, Hilaire Wangun та ін. "An Aniline-Mediated Regioselective Synthesis of Quinoxalin-2-ones via the Condensation of α-Ketimine Esters with 2-Aminoanilines". Synthesis 50, № 11 (2018): 2221–30. http://dx.doi.org/10.1055/s-0037-1609345.

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A highly regioselective method for the condensation of α-ketimine esters with 2-aminoanilines for the construction of quinoxalin-2-one derivatives is described. The substrate scope with 2-aminoaniline derivatives and different α-keto esters is explored with yields ranging from 44 to 90% and typical isolated regioselectivities between 6.4 to >25:1.

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3

Karthikeyan, Subramani, Thothadri Srinivasan, Elumalai Sundaravadivel, Muthusamy Kandaswamy, and Devadasan Velmurugan. "(Z)-3-(2-Aminoanilino)-1-phenylbut-2-en-1-one." Acta Crystallographica Section E Structure Reports Online 69, no. 5 (2013): o780. http://dx.doi.org/10.1107/s160053681301060x.

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4

M.A., LlKHATE, and S. FERNANDES P. "Synthesis of some Substituted-dibenzodiazepinones. A Tricyclic System." Journal of Indian Chemical Society Vol. 67, July 1990 (1990): 609–10. https://doi.org/10.5281/zenodo.6240604.

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Department of Chemistry. St. Xavier's College, Bombay-400 001 <em>Manuscript received 11 September 1989 revised 25 January 1990, accepted 30 March 1990</em> Synthesis of some Substituted-dibenzodiazepinones. A Tricyclic System

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5

Hammal, Lamouri, Samia Bouzroura, Chantal André, Bellara Nedjar‐Kolli, and Pascal Hoffmann. "Versatile Cyclization of Aminoanilino Lactones: Access to Benzotriazoles and Condensed Benzodiazepin‐2‐thiones." Synthetic Communications 37, no. 3 (2007): 501–11. http://dx.doi.org/10.1080/00397910601039259.

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6

Yuan, De-Qi, Kahee Fujita, Hidefumi Mizushima, and Masatoshi Yamaguchi. "Selective mono- and bis-condensations of isophthalaldehyde derivative with 6-(o-aminoanilino)cyclodextrins." Journal of the Chemical Society, Perkin Transactions 1, no. 21 (1997): 3135–36. http://dx.doi.org/10.1039/a705506d.

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7

Lu, Rong, Hua Xia, Xingqiang Lü, and Shunsheng Zhao. "(Z)-4-[(2-Aminoanilino)(phenyl)methylidene]-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one." Acta Crystallographica Section E Structure Reports Online 67, no. 10 (2011): o2701. http://dx.doi.org/10.1107/s1600536811037470.

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8

YUKI, Yasuo, Hideo KUNISADA, and Kiyotaka TAWARA. "Preparation of polyguanamine by self-polyaddition of 2-amino-4-(m-aminoanilino)-6-isopropenyl-1,3,5-triazine." NIPPON KAGAKU KAISHI, no. 1 (1987): 74–77. http://dx.doi.org/10.1246/nikkashi.1987.74.

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9

Dzvinchuk, I. B., and M. O. Lozinskii. "Isomerization of 2-Phenacyl-1H-benzimidazole Arylhydrazones to 1-Aryl-5-(o-aminoanilino)-3-phenylpyrazoles by Trifluoroacetylation and Hydrazinolysis." Chemistry of Heterocyclic Compounds 41, no. 7 (2005): 845–49. http://dx.doi.org/10.1007/s10593-005-0236-y.

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10

Renfrew, A. H. M., I. Bates, D. A. S. Phillips, T. Rosenau, T. Tomic та J. Xu. "Functionalisation of lyocell. Part 2: Synthesis of 6-p-aminoanilino-4-p-(β-sulphatoethylsulphonyl)anilino-1,3,5-triazin-2(1H)-one†". Coloration Technology 124, № 1 (2008): 56–61. http://dx.doi.org/10.1111/j.1478-4408.2007.00120.x.

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11

Akai, Nobuyuki, Satoshi Kudoh, and Munetaka Nakata. "UV Photolysis of 1,4-Diaminobenzene in a Low-Temperature Argon Matrix to 2,5-Cyclohexadiene-1,4-diimine via 4-Aminoanilino Radical." Journal of Physical Chemistry A 107, no. 34 (2003): 6725–30. http://dx.doi.org/10.1021/jp022694z.

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12

Okamoto, Yoshihisa, Yoshimi Yamaguchi, Kaname Takagi, Kazuho Harada, and Yoshihisa Kurasawa. "Ring Closure of 4-Substituted 1-Amino-1-(2-aminoanilino)-2,4-dicyanobuta-1,3-diene via 5-exo-Trig and 6-exo-Dig Process." HETEROCYCLES 51, no. 8 (1999): 1855. http://dx.doi.org/10.3987/com-99-8561.

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13

Yamaguchi, Yoshimi, Kaname Takagi, Yoshihisa Okamoto, Kazuho Harada, and Yoshihisa Kurasawa. "ChemInform Abstract: Ring Closure of 4-Substituted 1-Amino-1-(2-aminoanilino)-2,4-dicyanobuta-1,3-diene via 5-exo-trig and 6-exo-dig Process." ChemInform 30, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199945062.

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14

Takagi, Kaname, Tomoji Aotsuka, And Hikari Morita, and Yoshihisa Okamoto. "Synthesis of pyrimidino[4,5-b][1,5]benzodiazepin-2-ones and pyrimidino[1,6-a]benzimidazol-1-ones from 4-ethoxycarbonylamino-1H-1,5-benzodiazpine-3-carbonitrilevia4-(2-aminoanilino)pyrimidin-2(1H)-one-5-carbonitriles." Journal of Heterocyclic Chemistry 23, no. 5 (1986): 1443–49. http://dx.doi.org/10.1002/jhet.5570230539.

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15

Singh, Ram, and G. Geetanjali. "Synthesis of selected novel 7-methoxycarbonyl-10-substituted isoalloxazines." Journal of the Serbian Chemical Society 71, no. 6 (2006): 575–79. http://dx.doi.org/10.2298/jsc0606575s.

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The synthesis of selected novel 7-methoxycarbonyl-10-substituted isoalloxazines by the cyclocondensation of 2-substituted aminoanilines with alloxan monohydrate under acidic condition in 21-52 % yields, is described.

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16

Strashnova, S. B., O. V. Avramenko, M. N. Zhuk, O. V. Kovalchukova, P. V. Strashnov, and B. E. Zaitsev. "Synthesis and Study of Complexes of Copper(II), Zinc, Cobalt(II) and Nickel(II) with Nitrofluorenylidene-9-Amino(Imino) Derivatives." Chemistry Journal of Moldova 4, no. 2 (2009): 68–71. http://dx.doi.org/10.19261/cjm.2009.04(2).09.

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The complexes of general formula MCl2∙L1-4∙nH2O (where L1 - N-(2,4,7-trinitrofluorenilidene-9)-p-dimethyl-aminoanilin, L2 - N-(2,4,5,7-tetranitrofluorenilidene-9)-p-dimethylaminoaniline, L3 - N-(2,4,7-trinitrofluorenilidene)-N-(p-dimethylaminophenyl)hydroxylamine, L4 - N-(2,4,5,7-tetranitrofluorenilidene-9)-N-(p-dimethylaminophenyl)-hydroxylamine; M=Cu, Co, Ni, Zn; n= 1-3 have been synthesized and investigated by different methods. Spectral criteria of co-ordination of the molecules L1 –L4 in electronic adsorption spectra were detected.

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17

Abe, Noritaka, Naomi Ishikawa, Takashi Hayashi та Yoshiaki Miura. "Synthesis and Some Reactions of 2-(2-Aminoanilino)cyclohepta[b]pyrroles: Leading to 5H-Cyclohepta[1′,2′: 4,5]pyrrolo[2,3-b][1,5]benzodiazepine, a Novel 20π Antiaromatic System, and Cydohepta[1′,2′: 4,5] pyrrolo[1,2-a]benzimidazoles". Bulletin of the Chemical Society of Japan 63, № 6 (1990): 1617–22. http://dx.doi.org/10.1246/bcsj.63.1617.

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18

Detert, Heiner, and Volker Schmitt. "Acidochromism of stilbenoid chromophores with ap-aminoaniline centre." Journal of Physical Organic Chemistry 19, no. 8-9 (2006): 603–7. http://dx.doi.org/10.1002/poc.1091.

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19

Shaimaa hatem Abdullah. "Synthesis, diagnosis and biological activity study of some heterocyclic compounds derived from 2-aminobenzothiazole." Tikrit Journal of Pure Science 23, no. 4 (2018): 32–38. http://dx.doi.org/10.25130/tjps.v23i4.521.

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This study includes synthesis of some benzothiazole derivatives from treatment 2 -aminothiazole with choroacyle chloride to form 1-hydrogen-benzothiazole-2yl-2-chloroastiamide (1).the last one was reacted with urea, thiurea, thiosymigarizaide, 2- amibenzothiazole and para- aminoaniline, respectively to form the compounds (2,6). Some shiff bases for 2-aminobenzothiazole (7,8) were prepared from the reacting with aromatic aldehydes and it was cycled by reaction with glycine to form two derivatives of amidazolidine (9,10). The prepared compounds were diagnosed by IR spectra and H1NMR for proton,

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20

Mai, Antonello, Andrea Perrone, Angela Nebbioso, et al. "Novel uracil-based 2-aminoanilide and 2-aminoanilide-like derivatives: Histone deacetylase inhibition and in-cell activities." Bioorganic & Medicinal Chemistry Letters 18, no. 8 (2008): 2530–35. http://dx.doi.org/10.1016/j.bmcl.2008.03.055.

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21

Yalçınkaya, Süleyman, and Nureddin Çolak. "Synthesis and Characterization of Poly(Aniline-co-o-Aminoaniline)." Designed Monomers and Polymers 15, no. 2 (2012): 147–57. http://dx.doi.org/10.1163/156855511x615038.

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22

Porzelle, Achim, Michael D. Woodrow, and Nicholas C. O. Tomkinson. "Rearrangement Strategy for the Synthesis of 2-Aminoanilines." Organic Letters 12, no. 7 (2010): 1492–95. http://dx.doi.org/10.1021/ol100196a.

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23

Lovrinčević, Vilma, Dragana Vuk, Irena Škorić, and Nikola Basarić. "Chromo-Orthogonal Deprotection of Carboxylic Acids by Aminonaphthalene and Aminoaniline Photocages." Journal of Organic Chemistry 87, no. 5 (2022): 2489–500. http://dx.doi.org/10.1021/acs.joc.1c02407.

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24

Porzelle, Achim, Michael D. Woodrow, and Nicholas C. O. Tomkinson. "ChemInform Abstract: Rearrangement Strategy for the Synthesis of 2-Aminoanilines." ChemInform 41, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.201033067.

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25

Olsen, Stine T., and Kurt V. Mikkelsen. "First hyperpolarizability of para-aminoaniline induced by a variety of gold nano particles." Physical Chemistry Chemical Physics 18, no. 35 (2016): 24343–49. http://dx.doi.org/10.1039/c6cp01078d.

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26

Patch, Raymond J., Benjamin M. Brandt, Davoud Asgari, et al. "Potent 2′-aminoanilide inhibitors of cFMS as potential anti-inflammatory agents." Bioorganic & Medicinal Chemistry Letters 17, no. 22 (2007): 6070–74. http://dx.doi.org/10.1016/j.bmcl.2007.09.057.

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27

Ohara, Takumi, Masato Kaneda, Tomo Saito, Nobutaka Fujii, Hiroaki Ohno, and Shinya Oishi. "Head-to-tail macrocyclization of cysteine-free peptides using an o -aminoanilide linker." Bioorganic & Medicinal Chemistry Letters 28, no. 8 (2018): 1283–86. http://dx.doi.org/10.1016/j.bmcl.2018.03.027.

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28

Sathya, D., R. Jagan, R. Padmavathy, R. Mohan Kumar, and K. Sivakumar. "N—H...O, O—H...O hydrogen-bonded supramolecular sheet formation in the bis(2-aminoanilinium) fumarate, 3-methylanilinium hydrogen fumarate and 4-chloroanilinium hydrogen fumarate salts." Acta Crystallographica Section C Crystal Structure Communications 69, no. 8 (2013): 904–9. http://dx.doi.org/10.1107/s0108270113017629.

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In bis(2-aminoanilinum) fumarate, 2C6H9N2+·C4H2O42−, (I), the asymmetric unit consists of two aminoanilinium cations and one fumarate dianion, whereas in 3-methylanilinium hydrogen fumarate, C7H10N+·C4H3O4−, (II), and 4-chloroanilinium hydrogen fumarate, C6H7ClN+·C4H3O4−, (III), the asymmetric unit contains two symmetry-independent hydrogen fumate anions and anilinium cations with a slight difference in their geometric parameters; the two salts are isostructural. In (II) and (III), the carboxylic acid H atoms of the anions are disordered across both ends of the anion, with equal site occupanci

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29

Ma, P. P., H. L. Wu, and H. F. Gan. "Synthesis of 2-(Arylmethyl)benzazoles by the Sulfur-mediated Cyclization of 2-Aminophenol or 2-Aminoaniline with Arylacetylenes." Russian Journal of Organic Chemistry 59, no. 8 (2023): 1424–35. http://dx.doi.org/10.1134/s1070428023080171.

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30

von Bredow, Lukas, Thomas Martin Schäfer, Julian Hogenkamp, et al. "Synthesis, Antiplasmodial, and Antileukemia Activity of Dihydroartemisinin–HDAC Inhibitor Hybrids as Multitarget Drugs." Pharmaceuticals 15, no. 3 (2022): 333. http://dx.doi.org/10.3390/ph15030333.

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Artemisinin-based combination therapies (ACTs) are the gold standard for the treatment of malaria, but the efficacy is threatened by the development of parasite resistance. Histone deacetylase inhibitors (HDACis) are an emerging new class of potential antiplasmodial drugs. In this work, we present the design, synthesis, and biological evaluation of a mini library of dihydroartemisinin–HDACi hybrid molecules. The screening of the hybrid molecules for their activity against selected human HDAC isoforms, asexual blood stage P. falciparum parasites, and a panel of leukemia cell lines delivered imp

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31

Lamblin, Marc, Russell Spingarn, Tian-Tian Wang та ін. "Ano-Aminoanilide Analogue of 1α,25-Dihydroxyvitamin D3Functions as a Strong Vitamin D Receptor Antagonist". Journal of Medicinal Chemistry 53, № 20 (2010): 7461–65. http://dx.doi.org/10.1021/jm1007159.

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32

Liu, Jiaqi, Sarah Morgan, and Jessica M. Hoover. "Cobalt‐Catalyzed Aerobic Oxidative Cyclization of 2‐Aminoanilines with Isonitriles: Facile Access to 2‐Aminobenzimidazoles." ChemCatChem 12, no. 5 (2020): 1297–301. http://dx.doi.org/10.1002/cctc.201902011.

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33

Lakkadi, Arunapriya, Naveen Baindla, and Parthasarathy Tigulla. "Synthesis, Spectroscopic and Computational Studies of Charge-Transfer Complexation Between 4-Aminoaniline and 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone." Journal of Solution Chemistry 46, no. 12 (2017): 2171–90. http://dx.doi.org/10.1007/s10953-017-0685-9.

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34

Minisini, Martina, Eros Di Giorgio, Emanuela Kerschbamer, et al. "Transcriptomic and genomic studies classify NKL54 as a histone deacetylase inhibitor with indirect influence on MEF2-dependent transcription." Nucleic Acids Research 50, no. 5 (2022): 2566–86. http://dx.doi.org/10.1093/nar/gkac081.

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Abstract In leiomyosarcoma class IIa HDACs (histone deacetylases) bind MEF2 and convert these transcription factors into repressors to sustain proliferation. Disruption of this complex with small molecules should antagonize cancer growth. NKL54, a PAOA (pimeloylanilide o-aminoanilide) derivative, binds a hydrophobic groove of MEF2, which is used as a docking site by class IIa HDACs. However, NKL54 could also act as HDAC inhibitor (HDACI). Therefore, it is unclear which activity is predominant. Here, we show that NKL54 and similar derivatives are unable to release MEF2 from binding to class IIa

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35

Chęcińska, Lilianna, Jarosław Lewkowski, Magdalena Małecka, and Marek Dzięgielewski. "Synthesis and Characterization of N,N’-terephthalidenebis(o-aminoaniline): Crystal Structures of Its Two Polymorphic Forms Controlled by Changing the Crystallization Solvent." Journal of Chemical Crystallography 43, no. 8 (2013): 421–28. http://dx.doi.org/10.1007/s10870-013-0439-5.

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36

Losada, José, and M. Pilar García Armada. "A glucose amperometric sensor based on covalent immobilization of glucose oxidase in poly-2-aminoaniline film via chloranil on platinized platinum electrode." Electroanalysis 9, no. 18 (1997): 1416–21. http://dx.doi.org/10.1002/elan.1140091808.

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37

Ye, Jing, Tianxiang Hu, Hui Ding, and Xiawei Dong. "Synthesis of fluorescent 9-(4-aminoaniline)-acridine for highly specific and rapid detection of human serum albumin by fluorescence-capillary gel electrophoresis." Materials Express 13, no. 12 (2023): 2057–63. http://dx.doi.org/10.1166/mex.2023.2571.

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In clinical practice, many diseases can lead to changes in serum albumin concentration (HSA) in patients. Accurate detection of HSA concentration is of great significance for disease diagnosis. Based on this, this study designed and synthesized 9-(4-amino-aniline)-acridine (AAA) as a fluorescent probe. By laser induction and capillary gel electrophoresis (CGE), a new rapid and highly specific HSA detection method based on fluorescence-CGE was established. Various experimental control factors were investigated, and the optimal experimental conditions were determined as follows: the running buff

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38

Shi, Xinkang, Junmei Guo, Jianping Liu, Mingde Ye, and Qing Xu. "Unexpectedly Simple Synthesis of Benzazoles bytBuONa-Catalyzed Direct Aerobic Oxidative Cyclocondensation ofo-Thio/Hydroxy/Aminoanilines with Alcohols under Air." Chemistry - A European Journal 21, no. 28 (2015): 9988–93. http://dx.doi.org/10.1002/chem.201501184.

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39

Johnson, Byron S., David J. Burinsky, Svetlana A. Burova, Roman Davis, Russ N. Fitzgerald, and Richard T. Matsuoka. "Novel product ions of 2-aminoanilide and benzimidazole Ag(I) complexes using electrospray ionization with multi-stage tandem mass spectrometry." Rapid Communications in Mass Spectrometry 26, no. 9 (2012): 1115–22. http://dx.doi.org/10.1002/rcm.6210.

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40

Liu, Shuang, Zhengjie He, Wen-Yuan Hsieh, and Phillip E. Fanwick. "Synthesis, Characterization, and X-ray Crystal Structure of In(DOTA-AA) (AA =p-Aminoanilide): A Model for111In-Labeled DOTA-Biomolecule Conjugates." Inorganic Chemistry 42, no. 26 (2003): 8831–37. http://dx.doi.org/10.1021/ic0349914.

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41

Linus Obi, Ezenweke, Ojiako Eugenia Nonye, Esonwune Anacletus Anayochukwu, and Olugbue Victor U. "Chemical Synthesis and Microbial Evaluation of Iron (II) and Cobalt (II) Complexes of Schiff Base Dervived from ?-Hydroxynapthalene-1-Carbaldehyde Using 2-Aminoaniline and 2-Hydroxyaniline as the Aniline Di-Substituents." International Journal of Science and Research (IJSR) 10, no. 8 (2021): 949–61. https://doi.org/10.21275/sr21803191119.

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42

Shi, Xinkang, Junmei Guo, Jianping Liu, Mingde Ye, and Qing Xu. "ChemInform Abstract: Unexpectedly Simple Synthesis of Benzazoles by tBuONa-Catalyzed Direct Aerobic Oxidative Cyclocondensation of o-Thio/Hydroxy/Aminoanilines with Alcohols under Air." ChemInform 46, no. 46 (2015): no. http://dx.doi.org/10.1002/chin.201546038.

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43

Wang, Yanguang, Jin She, and Zheng Jiang. "One-Pot Synthesis of Functionalized Benzimidazoles and 1H-Pyrimidines via Cascade Reactions of o-Aminoanilines or Naphthalene-1,8-diamine with Alkynes and p-Tolylsulfonyl Azide." Synlett 2009, no. 12 (2009): 2023–27. http://dx.doi.org/10.1055/s-0029-1217515.

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44

KARATAŞ, Özgül, Yusuf CEYLAN, and Ziya Erdem KOÇ. "2,4,6-Tris(p-aminoanilino)-1,3,5-triazine: Synthesis and Electron Paramagnetic Resonance (EPR) Analysis." Sakarya University Journal of Science, October 10, 2022. http://dx.doi.org/10.16984/saufenbilder.1135112.

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A significant group of compounds arise from substituted s-triazine derivatives that have tripodal heterocyclic compound. Compounds classified as heterocyclic possible created the largest and most diverse family of organic compounds. In this study, we reported that a new template has been syntheses from a cyanuric chloride and its diamine derivative. The desired triamine a tripodal 2, 4, 6-tris (p-aminoaanilino)-1, 3, 5-triazine (C21H21N9), called to be TRIPOD, has been obtained from cyanuric chloride with 3 eq of p-phenylenediamine reaction in acetone. After synthesis, TRIPOD sample which was

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45

Hammal, Lamouri, Samia Bouzroura, Chantal Andre, Bellara Nedjar-Kolli, and Pascal Hoffmann. "Versatile Cyclization of Aminoanilino Lactones: Access to Benzotriazoles and Condensed Benzodiazepin-2-thiones." ChemInform 38, no. 26 (2007). http://dx.doi.org/10.1002/chin.200726031.

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46

Samba, Mohamed, Bahia Djerrari, Mohamed Said Minnih, Youssef Ramli, El Mokhtar Essassi, and Joel T. Mague. "(4Z)-4-[1-(2-Aminoanilino)ethylidene]-3-methyl-1-phenyl-4,5-dihydro-1H-pyrazol-5-one." IUCrData 2, no. 2 (2017). http://dx.doi.org/10.1107/s2414314617002565.

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The conformation of the title compound, C18H18N4O, is partly determined by an intramolecular N—H...O hydrogen bond that imposes planarity on the central aminoethylidene-3-methylpyrazol-5-one segment of the molecule. In the crystal, N—H...O hydrogen and N—H...N hydrogen bonds both form centrosymmetric dimers that encloseR22(18) rings. These, together with C—H...N and π–π stacking interactions between centrosymmetrically related pyrazalone rings, stack the molecules along theb-axis direction.

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47

Basha, N. Jeelan, CH Upendar Reddy, and Ν. M. Goudgaon. "CYCLIZATION OF 4-(2-AMINOANILINO)-2-BENZYLTHIOPYRIMIDINE TO NOVEL 1-(2-BENZYLTHIOPYRIMIDIN-4-YI)-2-SUBSTITUTED BENZIMIDAZOLES." Heterocyclic Communications 14, no. 6 (2008). http://dx.doi.org/10.1515/hc.2008.14.6.469.

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48

Dzvinchuk, I. B., and M. O. Lozinskii. "Isomerization of 2-Phenacyl-1H-benzimidazole Arylhydrazones to 1-Aryl-5-(o-aminoanilino)-3-phenylpyrazoles by Trifluoroacetylation and Hydrazinolysis." ChemInform 37, no. 17 (2006). http://dx.doi.org/10.1002/chin.200617123.

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49

Hong, Ziyong. "Review on the o‐aminoaniline Moiety in Peptide and Protein Chemistry." ChemBioChem, January 23, 2025. https://doi.org/10.1002/cbic.202401011.

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Peptides and proteins are important functional biomolecules both inside and outside of living organisms. The ability to prepare various types of functionalized peptides and proteins is essential for understanding fundamental biological processes, such as protein folding and post‐translational modifications (PTMs), and for developing new therapeutics for many diseases, such as cancers and neurodegenerative diseases. The o‐aminoaniline moiety was first proposed for activation to a thioester precursor and used for native chemical ligation to prepare large peptides and proteins. In the past decade

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Wang, Lin-Xuan, Bin Qiu, Xiaode An, Peizhen Dong, Ruibin Liu, and Jian Xiao. "Organocatalytic cascade aldimine condensation/[1,6]-hydride transfer/Mannich-type cyclization: sustainable access to indole-2,3-fused diazocanes." Green Chemistry, 2021. http://dx.doi.org/10.1039/d1gc02570h.

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Abstract:

An unprecedented organocatalytic cascade aldimine condensation/[1,6]-hydride transfer/Mannich-type cyclization of indole-2-carbaldehydes with o-aminoanilines was developed to assemble polycyclic indole-2,3-fused diazocanes in one-step. This novel methodology features high step- and atom-economy, redox-neutral,...

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