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- Unexpected N-glycosidation reaction of glycals with 1-amino-anthracene: structure revision and application to the synthesis of new analogues of marmycin A. Xuefeng Zhang, Xiaolong Jiang, Chunyong Ding, Qizheng Yao, Ao Zhang
, Org. Biomol. Chem.
, 2013
, 11
, 1383
- Dansyl-anthracene dyads for ratiometric fluorescence recognition of Cu2+. Kuljit Kaur, Subodh Kumar
, Dalton Trans.
, 2011
, 40
, 2451
- Oligo Tröger's bases—new molecular scaffolds. Bohumil Dolenský, Martin Havlík, Vladimír Král
, Chem. Soc. Rev.
, 2012
, 41
, 3839
- Selective Diels–Alder cycloaddition on semiconducting single-walled carbon nanotubes for potential separation application. Jiao-Tong Sun, Lu-Yang Zhao, Chun-Yan Hong, Cai-Yuan Pan
, Chem. Commun.
, 2011
, 47
, 10704
- Efficient amidation of weak amines: synthesis, chiral separation by SFC, and antimicrobial activity of N-(9,10-dioxo-9,10-dihydroanthracen-1-yl) carboxamide. Kathiravan Asokan, A. Zahir Hussain, Andivelu Ilangovan
, Org. Biomol. Chem.
, 2024
, 22
, 309
- Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol. Yuan Gao, Mengfan Zhang, Chaoyu Wang, Zhen Yang, Xianqiang Huang, Ruokun Feng, Chenze Qi
, Chem. Commun.
, 2020
, 56
, 14231
- Communication. Cyclodextrin-modified micellar electrokinetic chromatography combined with semiconductor laser fluorimetry. Totaro Imasaka, Kiyohiro Nishitani, Nobuhiko Ishibashi
, Analyst
, 1991
, 116
, 1407
- Fluorescence and absorption spectra of anthracene crystals at 4 K doped with 1- and 2-aminoanthracene: effects of guest orientation. N. James Bridge, David Vincent
, J. Chem. Soc., Faraday Trans. 2
, 1974
, 70
, 30
- Characteristics of key intermediates generated in uncatalyzed bis(2,4-dinitrophenyl) oxalate (DNPO) chemiluminescence reactions. Ji Hoon Lee, James C. Rock, Mark A. Schlautman, Elizabeth R. Carraway
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 1653
- Applications of Friedel–Crafts reactions in total synthesis of natural products. Majid M. Heravi, Vahideh Zadsirjan, Pegah Saedi, Tayebeh Momeni
, RSC Adv.
, 2018
, 8
, 40061