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- Friedel–Crafts acylations of aromatic hydrocarbons. Part XIV. Monoacetylation and monobenzoylation of 2,7-dimethylnaphthalene. P. H. Gore, A. S. Siddiquei
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 1442
- Friedel–Crafts reactions. Part XXIV. Diacylations of 2,7-dimethylnaphthalene. Deuterium-labelling as an aid to structural determinations. Peter H. Gore, Adhid Y. Miri, Asif S. Siddiquei
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 2936
- The selective oxidation of substituted aromatic hydrocarbons and the observation of uncoupling via redox cycling during naphthalene oxidation by the CYP101B1 system. Emma A. Hall, Md Raihan Sarkar, Stephen G. Bell
, Catal. Sci. Technol.
, 2017
, 7
, 1537
- Development of a methodology for accurate quantitation of alkylated polycyclic aromatic hydrocarbons in petroleum and oil contaminated environmental samples. Chun Yang, Gong Zhang, Zhendi Wang, Zeyu Yang, Bruce Hollebone, Mike Landriault, Keval Shah, Carl E. Brown
, Anal. Methods
, 2014
, 6
, 7760
- A bis-urea naphthalene
macrocycle displaying two crystal structures with parallel ureas. Michael F. Geer, Mark D. Smith, Linda S. Shimizu
, CrystEngComm
, 2011
, 13
, 3665
- Preparation of a range of NNN′N′-tetrasubstituted 1,8-diaminonaphthalenes. Roger W. Alder, Martin R. Bryce, Nigel C. Goode, Nigel Miller, Judith Owen
, J. Chem. Soc., Perkin Trans. 1
, 1981
, 2840
- 243. Eight- and higher-membered ring compounds. Part V. Di-(naphthalene-2 : 7-dimethylene) and its conversion into coronene. Wilson Baker, F. Glockling, J. F. W. McOmie
, J. Chem. Soc.
, 1951
, 1118
- 16. Homologues of naphthacene. Part II. 2-Methyl- and 2 : 7-dimethyl-naphthacene: synthetic applications of 2 : 6- and -2 : 7-dimethyl-1 : 2 : 3 : 4-tetrahydronaphthalene. Edward A. Coulson
, J. Chem. Soc.
, 1935
, 77
- 180. Side-chain bromination of some alkylnaphthalenes with N-bromosuccinimide. Ng. Ph. Buu-Hoï, Jean Lecocq
, J. Chem. Soc.
, 1946
, 830
- Gas-phase thermochemistry of polycyclic aromatic hydrocarbons: an approach integrating the quantum chemistry composite scheme and reaction generator. Irina Minenkova, Arseniy A. Otlyotov, Luigi Cavallo, Yury Minenkov
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 3163