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Journal articles on the topic 'Bromobenzamide'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Xing, Zhi-Tao, Hai-Bo Wang, Jun Yin, Wen-Yuan Wu, and Feng Han. "4-Bromobenzamide oxime." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2236—o2237. http://dx.doi.org/10.1107/s1600536807015863.

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2

Cavalheiro, Valéria Machado Siqueira, Sabrina Madruga Nobre, and Felipe Kessler. "Correction: Study of the dual functional behaviour of 1,2-bis(4-bromobenzamide)benzene by synchronous fluorescence spectroscopy." New Journal of Chemistry 43, no. 24 (2019): 9740. http://dx.doi.org/10.1039/c9nj90078k.

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Correction for ‘Study of the dual functional behaviour of 1,2-bis(4-bromobenzamide)benzene by synchronous fluorescence spectroscopy’ by Valéria Machado Siqueira Cavalheiro et al., New J. Chem., 2019, 43, 7162–7168.

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3

Cavalheiro, Valéria Machado Siqueira, Sabrina Madruga Nobre, and Felipe Kessler. "Study of the dual functional behaviour of 1,2-bis(4-bromobenzamide)benzene by synchronous fluorescence spectroscopy." New Journal of Chemistry 43, no. 18 (2019): 7162–68. http://dx.doi.org/10.1039/c8nj06066e.

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This study presents the dual functionality of 1,2-bis(4-bromobenzamide)benzene, where depending on the stoichiometric conditions, temperature and reaction time, the compound may act as a PdCl<sub>2</sub> ligand or as one of the reactants of the Suzuki coupling reaction.

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4

B., THIMME GOWDA, JAGAN MOHANA RAO P., and DARLIN QUINE S. "Kinetics and Mechanism of Bromination of Phenol and Substituted Phenols by N-Bromobenzamide in Aquo-acetic Acid Medium." Journal of Indian Chemical Society Vol. 69, Dec 1992 (1992): 830–34. https://doi.org/10.5281/zenodo.6116677.

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Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangothri-574 199 <em>Manuscript received 2 December 1991, revised 24 August 1992, accepted 24 September 1992</em> Kinetics of bromination of phenol and substituted phenols by <em>N</em>-bromobenzamide <em>have </em>been studied in aquo-acetic acid (1 : 1, v/v) medium. The rates of bromination show first order kinetics in [NBB], fractional order in [phenols] and zero order in [H<sup>+</sup>]. The rate slightly decreases with the addition of the reduced product of the oxidant, while the increase in aceti

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5

Y., Dominic Ravichandran, Kishor Rachna, Hariharasubramanian A., Mohana Priya K., and S. Khora Samanta. "Synthesis and characterization of N-substituted benzimidazole derivatives and study of their antibacterial and antifungal activity." Journal of Indian Chemical Society Vol. 92, Jun 2015 (2015): 915–17. https://doi.org/10.5281/zenodo.5637656.

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Organic Chemistry Division, School of Advanced Sciences, VIT University, Vellore-632 014, Tamilnadu, India <em>E-mail </em>: dominic.y@vit.ac.in Medical Biotechnology Division, School of Bioscience and Technology, VIT University, Vellore-632 014, Tamilnadu, India N-(4-(1<em>H</em>-Benzo[d]imidazol-1-yl)phenyl)-3-nitrobenzamide, N-(4-(1<em>H</em>-benzo[d]imidazol-1-yl)phenyl)-4- chlorobenzamide, 4-(1<em>H</em>-benzo[d]imidazol-1-yl)benzenamine and N-(4-(1<em>H</em>-benzo[<em>d</em>]imidazol-1-yl)phenyl)-4-bromobenzamide were synthesized and characterized by IR and NMR techniques. These N-substi

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6

Hu, Rong-Hua, Yan Sui, Ji-Wu Wen, Zhi-Gang Luo, and Long-Jin Zhong. "A New Type of Organic Ferroelectric N-Dehydroabietyl-4-bromobenzamide." Asian Journal of Chemistry 27, no. 7 (2015): 2627–29. http://dx.doi.org/10.14233/ajchem.2015.18628.

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7

Liu, Zibin, Li-Yan Zeng, Chao Li, et al. "“On-Water” Synthesis of Quinazolinones and Dihydroquinazolinones Starting from o-Bromobenzonitrile." Molecules 23, no. 9 (2018): 2325. http://dx.doi.org/10.3390/molecules23092325.

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A versatile and practical “on-water” protocol was newly developed to synthesize quinazolinones using o-bromobenzonitrile as a novel starting material. Studies have found that air as well as water plays an important role in synthesis of quinazolinones. Further investigation indicated that dihydroquinazolinones can be prepared with this protocol under the protection of N2. The protocol can be extended to other substrates and various quinazolinones and dihydroquinazolinones were obtained. o-Bromobenzamide, o-aminobenzonitrile, and o-aminobenzamide were also evaluated as starting materials, and th

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8

Huang, Yu-Ying, Hui-Chang Lin, Kaung-Min Cheng, et al. "Efficient di-bromination of 5-pyrazolones and 5-hydroxypyrazoles by N-bromobenzamide." Tetrahedron 65, no. 46 (2009): 9592–97. http://dx.doi.org/10.1016/j.tet.2009.09.055.

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9

Chowdhury, Kakuli, and Kalyan K. Banerji. "Kinetics and mechanism of the oxidation of organic sulfides by N-bromobenzamide." Journal of Organic Chemistry 55, no. 19 (1990): 5391–93. http://dx.doi.org/10.1021/jo00306a017.

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10

Banerji, Kalyan K. "Kinetics and mechanism of the oxidation of substituted benzaldehydes by N-bromobenzamide." Journal of Organic Chemistry 51, no. 25 (1986): 4764–67. http://dx.doi.org/10.1021/jo00375a004.

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11

Aroonrerk, Nuntana, Nattisa Niyomtham, and Boon-ek Yingyoungnarongkul. "Anti-Inflammation of N-Benzyl-4-Bromobenzamide in Lipopolysaccharide-Induced Human Gingival Fibroblasts." Medical Principles and Practice 25, no. 2 (2015): 130–36. http://dx.doi.org/10.1159/000442164.

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12

Brijesh, Pare, W. Bhagwat V., Radhakrishnan Asha, and V. R. Shastry (late). "Kinetics and mechanism of micellar catalyzed autoxidation of ethanol, propanol and n-butanol by N-bromobenzamide." Journal of Indian Chemical Society Vol. 80, Aug 2003 (2003): 787–89. https://doi.org/10.5281/zenodo.5836582.

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Madhav Science College, School of Studies in Chemistry, Vikram University, Ujjain-456 010, India <em>E-mail</em> : brijesh_pare@hotmail.com <em>Manuscript received 4 June 2001. revised 21 January 2003, accepted 4 March 2003</em> A micellar catalyzed oxidation of ethanol, propanol and <em>n</em>-butanol by N-bromobenzamide (NBB) in acidic medium has been studied using sodium dodecyl sulfate. The cause of autocatalysis has been attributed to Br<sup>-</sup> ions, which was further substantiated by the removal of first stage on initial addition of potassium bromide. The pre-micellar catalysis by s

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13

BADOLE, M. K., L. N. MALVIYA, K. S. SARIYA, and V. K. SIRIAH. "Kinetic and Mechanistic Studies in the Oxidation of Ethanol by p-Methoxy-N-Bromobenzamide." Oriental Journal Of Chemistry 28, no. 3 (2012): 1433–36. http://dx.doi.org/10.13005/ojc/280345.

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14

Keskin, Ebru, Ummuhan Solmaz, Gun Binzet, Ilkay Gumus, and Hakan Arslan. "Synthesis, characterization and crystal structure of platinum(II) complexes with thiourea derivative ligands." European Journal of Chemistry 9, no. 4 (2018): 360–68. http://dx.doi.org/10.5155/eurjchem.9.4.360-368.1774.

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Thiourea derivatives [N-(di-n-propylcarbamothioyl)-4-fluorobenzamide (HL1) and N-(di-n-propylcarbamothioyl)-4-bromobenzamide (HL2)] and their platinum complexes have been successfully synthesized and structurally characterized by spectroscopic 1H NMR, 13C NMR, COSY, HMQC, and FT-IR techniques. The structure of both complexes was also confirmed by single crystal X-ray diffraction studies. The study of X-ray single crystal diffraction shows that the supramolecular aggregation of the complexes is stabilized via weak interactions as well as stacking interactions such as C-H···π and π···π. The cis-

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15

Banerji, Kalyan K. "Separation of polar and steric effects in the oxidation of ortho-substituted benzaldehydes by N-bromobenzamide." Proceedings / Indian Academy of Sciences 100, no. 5 (1988): 397–403. http://dx.doi.org/10.1007/bf02840578.

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16

Il’in, A. I., I. V. Kulakov, N. V. Leonova, S. S. Kasymbekova, O. V. Shchukina, and D. V. Barinov. "Synthesis and antibacterial activity of (N-1-methylglucosaminocarbonothioyl)-4-bromobenzamide chelate complex with copper(II) sulfate." Russian Journal of General Chemistry 81, no. 6 (2011): 1171–74. http://dx.doi.org/10.1134/s1070363211060168.

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17

Mahesha, Ninganayaka, Hemmige S. Yathirajan, Holalagudu A. Nagma Banu, Balakrishna Kalluraya, Sabine Foro, and Christopher Glidewell. "Different patterns of supramolecular aggregation in three amides containing N-(benzo[d]thiazolyl) substituents." Acta Crystallographica Section E Crystallographic Communications 77, no. 5 (2021): 504–11. http://dx.doi.org/10.1107/s2056989021003637.

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Crystal structures are reported for three amides containing N-benzo[d]thiazole substituents. In N-(benzo[d]thiazol-6-yl)-3-bromobenzamide, C14H9BrN2OS, where the two ring systems are nearly parallel to one another [dihedral angle = 5.8 (2)°], the molecules are linked by N—H...O and C—H...N hydrogen bonds to form ribbons of R 3 3(19) rings, which are linked into sheets by short Br...Br interactions [3.5812 (6) Å]. N-(6-Methoxybenzo[d]thiazol-2-yl)-2-nitrobenzamide, C15H11N3O4S, crystallizes with Z′ = 2 in space group Pna21: the dihedral angles between the ring systems [46.43 (15) and 66.35 (13)

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18

Tothadi, Srinu, Sumy Joseph, and Gautam R. Desiraju. "Synthon Modularity in Cocrystals of 4-Bromobenzamide withn-Alkanedicarboxylic Acids: Type I and Type II Halogen···Halogen Interactions." Crystal Growth & Design 13, no. 7 (2013): 3242–54. http://dx.doi.org/10.1021/cg400735f.

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19

B., THIMME GOWDA, JAGAN MOHANA RAO P., and DARLIN QUINE S. "Kinetics and Mechanism of Bromination of Phenol and Substituted Phenols by N-Bromobenzamide in Aquo-acetic Acid Medium." Journal of Indian Chemical Society Vol. 69, Dec 1992 (1992): 830–34. https://doi.org/10.5281/zenodo.6032293.

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Department of Post-Graduate Studies and Research in Chemistry, Mangalore University, Mangalagangothri-574 199 <em>Manuscript received 2 December 1991, revised 24 August 1992, accepted 24 September 1992</em> Kinetics of bromination of phenol and substituted phenols by <em>N</em>-b-omobenzamide <em>have </em>been studied in aquo-acetic acid (1 : 1, v/v) medium. The rates of bromination show first order kinetics in [NBB], fractional order in [phenols] and zero order in [H<sup>+</sup>]. The rate slightly decreases with the addition of the reduced product of the oxidant, while the increase in aceti

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20

Wang, Fei, Chao Chen, Geng Deng, and Chanjuan Xi. "Concise Approach to Benzisothiazol-3(2H)-one via Copper-Catalyzed Tandem Reaction of o-Bromobenzamide and Potassium Thiocyanate in Water." Journal of Organic Chemistry 77, no. 8 (2012): 4148–51. http://dx.doi.org/10.1021/jo300250x.

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21

Wang, Fei, Chao Chen, Geng Deng, and Chanjuan Xi. "ChemInform Abstract: Concise Approach to Benzisothiazol-3-(2H)-one via Copper-Catalyzed Tandem Reaction of o-Bromobenzamide and Potassium Thiocyanate in Water." ChemInform 43, no. 33 (2012): no. http://dx.doi.org/10.1002/chin.201233148.

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22

Sintov, Amnon C., Peter Ji Zhang, and Bozena B. Michniak-Kohn. "Cutaneous biotransformation of N-(4-bromobenzoyl)-S,S-dimethyliminosulfurane and its product, 4-bromobenzamide, leading to percutaneous penetration enhancement of drugs: Initial evidence using hydrocortisone." Journal of Controlled Release 133, no. 1 (2009): 44–51. http://dx.doi.org/10.1016/j.jconrel.2008.09.084.

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23

Guo, Shenghai, Yan Li, Li Tao, Wenwen Zhang, and Xuesen Fan. "Rapid assembly of quinazolinone scaffold via copper-catalyzed tandem reaction of 2-bromobenzamides with aldehydes and aqueous ammonia: application to the synthesis of the alkaloid tryptanthrin." RSC Adv. 4, no. 103 (2014): 59289–96. http://dx.doi.org/10.1039/c4ra10799c.

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24

Shinde, Mahesh H., and Umesh A. Kshirsagar. "A copper catalyzed multicomponent cascade redox reaction for the synthesis of quinazolinones." RSC Advances 6, no. 58 (2016): 52884–87. http://dx.doi.org/10.1039/c6ra10997g.

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A copper catalyzed multicomponent cascade redox reaction for the synthesis of various quinazolinones starting from easily available 2-bromobenzamides, benzylic alcohols and sodium azide as a nitrogen source has been developed.

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25

Abe, Takumi, Yuka Takahashi, Yuki Matsubara, and Koji Yamada. "An Ullmann N-arylation/2-amidation cascade by self-relay copper catalysis: one-pot synthesis of indolo[1,2-a]quinazolinones." Organic Chemistry Frontiers 4, no. 11 (2017): 2124–27. http://dx.doi.org/10.1039/c7qo00549k.

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We have developed a self-relay copper(i)-catalyzed Ullmann N-arylation/2-amidation cascade to form functionalized indolo[1,2-a]quinazolinones in one-pot from easily available indoles with 2-bromobenzamides.

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26

Sow, Salif, Mariama Thiam, Felix Odame, et al. "Crystal structure of 1-(1,3-benzothiazol-2-yl)-3-(4-bromobenzoyl)thiourea." Acta Crystallographica Section E Crystallographic Communications 80, no. 6 (2024): 663–66. http://dx.doi.org/10.1107/s2056989024004742.

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The chemical reaction of 4-bromobenzoylchloride and 2-aminothiazole in the presence of potassium thiocyanate yielded a white solid formulated as C15H10BrN3OS2, which consists of 4-bromobenzamido and 2-benzothiazolyl moieties connected by a thiourea group. The 4-bromobenzamido and 2-benzothiazolyl moieties are in a trans conformtion (sometimes also called s-trans due to the single bond) with respect to the N—C bond. The dihedral angle between the mean planes of the 4-bromophenyl and the 2-benzothiazolyl units is 10.45 (11)°. The thiourea moiety, —C—NH—C(=S) —NH— fragment forms a dihedral angle

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27

Xu, Lanting, Xianhua Pan, Yanyu Chen, et al. "Ligand-Controlled Chemoselective One-Pot Synthesis of Dibenzothiazepinones and Dibenzoxazepinones via Twice Copper-Catalyzed Cross-Coupling." Synlett 28, no. 10 (2017): 1201–8. http://dx.doi.org/10.1055/s-0036-1558959.

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A highly efficient and generally applicable protocol, starting from 2-bromobenzamides and 2-bromo(thio)phenols via twice copper-catalyzed couplings to afford dibenzothiazepines and dibenzoxazepinones has been developed. High levels of yield and chemoselectivity are achieved in a single-pot reaction by using an appropriate ligand. Moreover, this facile methodology allows rapid access to a variety of bioactive compounds and known psychotropic drug, which should broaden its application in organic synthesis.

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28

Aman, Hasil, Yu-Chiao Huang, Yu-Hao Liu, et al. "Cobalt-Catalyzed Cyclization of 2-Bromobenzamides with Carbodiimides: A New Route for the Synthesis of 3-(Imino)isoindolin-1-ones." Molecules 26, no. 23 (2021): 7212. http://dx.doi.org/10.3390/molecules26237212.

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A novel synthetic pathway to approach 3-(imino)isoindolin-1-ones by the Co-catalyzed cyclization reaction of 2-bromobenzamides with carbodiimides has been developed. This catalytic reaction can tolerate a variety of substituents and provide corresponding products in moderate yields for most cases. According to the literature, the reaction mechanism is proposed through the formation of a five-membered aza-cobalacycle complex, which carries out the following reaction subsequence, including nucleophilic addition and substitution, to furnish the desired structures.

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29

Hendi, Mukta S., Kenneth J. Natalie, Shivakumar B. Hendi, James A. Campbell, Thomas D. Greenwood, and James F. Wolfe. "Aromatic heteroannulation via ortho lithiation-cyclization of N-acyl-2-bromobenzamides." Tetrahedron Letters 30, no. 3 (1989): 275–78. http://dx.doi.org/10.1016/s0040-4039(00)95178-5.

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30

Chang, Yu-Wei, та Jing-Jun Yang. "trans-Bis[2-(2-bromobenzamido)-1,3-oxazoline(1−)-κ2N1,O]copper(II)". Acta Crystallographica Section E Structure Reports Online 63, № 8 (2007): m2126. http://dx.doi.org/10.1107/s1600536807033272.

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31

Krasikova, V., and M. Katkevics. "Preparation of benzisothiazolones from 2-bromobenzamides and sulfur under copper catalysis conditions." Chemistry of Heterocyclic Compounds 48, no. 11 (2013): 1684–90. http://dx.doi.org/10.1007/s10593-013-1193-5.

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32

Krasikova, V., and M. Katkevics. "ChemInform Abstract: Preparation of Benzisothiazolones from 2-Bromobenzamides and Sulfur under Copper Catalysis Conditions." ChemInform 44, no. 34 (2013): no. http://dx.doi.org/10.1002/chin.201334130.

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33

Chen, Lu, Christian Bruneau, Pierre H. Dixneuf, and Henri Doucet. "Palladium-Catalysed Regioselective Direct Arylations of Heteroarenes by Bromobenzamides: Direct Synthesis of Heteroaryl Benzamides." ChemCatChem 5, no. 7 (2013): 1956–63. http://dx.doi.org/10.1002/cctc.201200867.

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34

Ma, Dawei, Hexiang Wang, Kun Gao та Yongwen Jiang. "Assembly of Substituted Homophthalimides via CuI-Catalyzed Coupling of 2-Bromobenzamides with β-Keto Ester". HETEROCYCLES 79, № 1 (2009): 695. http://dx.doi.org/10.3987/com-08-s(d)36.

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35

Xi, Chanjuan, Shangjun Cai, and Fei Wang. "Synthesis of 3-Substituted Isocoumarin Derivatives via CuI-Catalyzed Reaction of o-Bromobenzamides with 1,3-Diketones." Synthesis 44, no. 12 (2012): 1892–97. http://dx.doi.org/10.1055/s-0031-1290949.

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36

Belvisi, Laura, Cesare Gennari, Giovanni Poli, Carlo Scolastico, and Barbara Salom. "Stereoselective radical-mediated cyclization of norephedrine derived o-bromobenzamides: Enantioselective synthesis of 4-substituted 1,2,3,4-tetrahydroisoquinolines." Tetrahedron: Asymmetry 4, no. 2 (1993): 273–80. http://dx.doi.org/10.1016/s0957-4166(00)82347-2.

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37

Chen, Lu, Christian Bruneau, Pierre H. Dixneuf, and Henri Doucet. "ChemInform Abstract: Palladium-Catalyzed Regioselective Direct Arylations of Heteroarenes by Bromobenzamides: Direct Synthesis of Heteroaryl Benzamides." ChemInform 44, no. 46 (2013): no. http://dx.doi.org/10.1002/chin.201346064.

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38

Ishibashi, Hiroyuki, Hirotaka Kawanami, and Masazumi Ikeda. "Sulfur-controlled 5-exo selective aryl radical cyclisation of N-vinylic 2-bromobenzamides: synthesis of lennoxamine and chilenine." Journal of the Chemical Society, Perkin Transactions 1, no. 6 (1997): 817–22. http://dx.doi.org/10.1039/a606723i.

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39

Wang, Fei, Peng Zhao, and Chanjuan Xi. "Copper-catalyzed one-pot synthesis of 2-thioxo-2,3-dihydroquinazolin-4(1H)-ones from ortho-bromobenzamides and isothiocyanates." Tetrahedron Letters 52, no. 2 (2011): 231–35. http://dx.doi.org/10.1016/j.tetlet.2010.11.010.

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40

Lo, Lee-Chiang, Nina Berova, Koji Nakanishi, Ezequiel Q. Morales, and Jesús T. Vázquez. "Circular dichroic studies of 2-amino-2-deoxy-galactopyranosides - conformations of the 2-(N-acetyl-p-bromobenzamido) group." Tetrahedron: Asymmetry 4, no. 3 (1993): 321–30. http://dx.doi.org/10.1016/s0957-4166(00)86076-0.

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41

Cai, Shangjun, Fei Wang, and Chanjuan Xi. "ChemInform Abstract: Synthesis of 3-Substituted Isocoumarin Derivatives via CuI-Catalyzed Reaction of o-Bromobenzamides with 1,3-Diketones." ChemInform 43, no. 41 (2012): no. http://dx.doi.org/10.1002/chin.201241148.

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42

BELVISI, L., C. GENNARI, G. POLI, C. SCOLASTICO, and B. SALOM. "ChemInform Abstract: Stereoselective Radical-Mediated Cyclization of Norephedrine Derived o- Bromobenzamides: Enantioselective Synthesis of 4-Substituted 1,2,3,4- Tetrahydroisoquinolines." ChemInform 24, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199325067.

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43

Zhao, Hong, Yichao Wu, Tin Wei та Mingzhong Cai. "Heterogeneous Copper-Catalysed Cascade Reactions of 2-Bromobenzamides with β-Keto Esters Leading to Isoquinolin-1(2H)-One Derivatives". Journal of Chemical Research 38, № 10 (2014): 634–38. http://dx.doi.org/10.3184/174751914x14117512932816.

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44

Toniolo, Claudio, Fernando Formaggio, Marco Crisma, Hans E. Schoemaker, and Johan Kamphuis. "The p-bromobenzamido chromophore as a circular dichroic probe for the assignment of the screw sense of helical peptides." Tetrahedron: Asymmetry 5, no. 4 (1994): 507–10. http://dx.doi.org/10.1016/0957-4166(94)80004-9.

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45

ISHIBASHI, H., H. KAWANAMI, and M. IKEDA. "ChemInform Abstract: Sulfur-Controlled 5-exo Selective Aryl Radical Cyclization of N- Vinylic 2-Bromobenzamides: Synthesis of Lennoxamine and Chilenine." ChemInform 28, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199733293.

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46

LO, L. C., N. BEROVA, K. NAKANISHI, E. Q. MORALES, and J. T. VAZQUEZ. "ChemInform Abstract: Circular Dichroic Studies of 2-Amino-2-deoxy-galactopyranosides - Conformations of the 2-(N-Acetyl-p-bromobenzamido) Group." ChemInform 24, no. 29 (2010): no. http://dx.doi.org/10.1002/chin.199329234.

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47

Wang, Fei, Peng Zhao, and Chanjuan Xi. "ChemInform Abstract: Copper-Catalyzed One-Pot Synthesis of 2-Thioxo-2,3-dihydroquinazolin-4(1H)-ones from ortho-Bromobenzamides and Isothiocyanates." ChemInform 42, no. 15 (2011): no. http://dx.doi.org/10.1002/chin.201115168.

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48

Zhao, Hong, Yichao Wu, Tin Wei та Mingzhong Cai. "ChemInform Abstract: Heterogeneous Copper-Catalyzed Cascade Reactions of 2-Bromobenzamides with β-Keto Esters Leading to Isoquinolin-1(2H)-one Derivatives." ChemInform 46, № 19 (2015): no. http://dx.doi.org/10.1002/chin.201519206.

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49

Li, Li, Miao Wang, Xiaojing Zhang, Yongwen Jiang, and Dawei Ma. "Assembly of Substituted 3-Methyleneisoindolin-1-ones via a CuI/l-Proline-Catalyzed Domino Reaction Process of 2-Bromobenzamides and Terminal Alkynes." Organic Letters 11, no. 6 (2009): 1309–12. http://dx.doi.org/10.1021/ol9000922.

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Hoshino, Osamu, Hiromichi Ogasawara, Akihisa Hirokawa, and Bunsuke Umezawa. "A Photolysis ofN-[3-(2-Hydroxy-3-methoxyphenyl)propyl]-6-bromobenzamides. One-step Synthesis of 5,6-Dihydro-4H,8H-pyrido[3,2,1-de]phenanthridin-8-ones." Chemistry Letters 17, no. 10 (1988): 1767–68. http://dx.doi.org/10.1246/cl.1988.1767.

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