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Cp*Rh(iii)-catalyzed and solvent-controlled tunable [4 + 1]/[4 + 3] annulation for the divergent assembly of dihydrobenzo[cd]indoles and dihydronaphtho[1,8-bc]azepines. Zhuo-Zhuo Zhang, Ya Li, Bing-Feng Shi , Org. Chem. Front. , 2022 , 9 , 3262

The reaction of nitrous acid with alcoholic alpha-naphthylamine hydrochloride and its application to the absorptiometric determination of nitrites. C. A. Parker , Analyst , 1949 , 74 , 112

A new entry to phenanthridine ring systems via sequential application of Suzuki and the modified Pictet–Spengler reactions. Anil K. Mandadapu, Mohammad Saifuddin, Piyush K. Agarwal, Bijoy Kundu , Org. Biomol. Chem. , 2009 , 7 , 2796

In situ synthesis of a GO/COFs composite with enhanced adsorption performance for organic pollutants in water. Li Liang, Jia Chen, Xuwei Chen, Jianhua Wang, Hongdeng Qiu , Environ. Sci.: Nano , 2022 , 9 , 554

Studies on the rearrangement of 1-¹ and 2-naphthylsulphamic acids. W. J. Spillane, F. L. Scott, C. B. Goggin , J. Chem. Soc. B , 1971 , 2409

Conformational variety of flexible mono-dentate ligands in coordination compounds: influence of π-involving interactions. Hamid Reza Khavasi, Sima Kavand , Dalton Trans. , 2016 , 45 , 10761

Revitalizing the aromatic aza-Claisen rearrangement: implications for the mechanism of ‘on-water’ catalysis. Kaitlin D. Beare, Christopher S. P. McErlean , Org. Biomol. Chem. , 2013 , 11 , 2452

LXXV.—A study of the substitution products of ar-tetrahydro-α-naphthylamine. 4-Bromotetrahydro-α-naphthylamine and ar-tetrahydro-α-naphthylamine-4-sulphonic acid. Gilbert Thomas Morgan, Frances Mary Gore Micklethwait, Herbert Ben Winfield , J. Chem. Soc., Trans. , 1904 , 85 , 736

C8–H bond activation vs. C2–H bond activation: from naphthyl amines to lactams. Renyi Shi, Lijun Lu, Hangyu Xie, Jingwen Yan, Ting Xu, Hua Zhang, Xiaotian Qi, Yu Lan, Aiwen Lei , Chem. Commun. , 2016 , 52 , 13307

Machine-learning-assisted molecular design of phenylnaphthylamine-type antioxidants. Shanda Du, Xiujuan Wang, Runguo Wang, Ling Lu, Yanlong Luo, Guohua You, Sizhu Wu , Phys. Chem. Chem. Phys. , 2022 , 24 , 13399