Paper
NJC
18 X. Su, M. D. Liptak and I. Aprahamian, Chem. Commun.,
2013, 49, 4160–4162.
19 Y. Liu, W. Yan, Y. Chen, J. L. Petersen and X. Shi, Org. Lett.,
2008, 10, 5389–5392.
of tailor-made fluorescent compounds. Moreover, accessible
reactive sites in our compounds hint at post-functionalization
opportunities.
20 Y. Zhang, X. Ye, J. L. Petersen, M. Li and X. Shi, J. Org.
Chem., 2015, 80, 3664–3669.
Conflicts of interest
21 Y. C. Zhang, R. Jin, L. Y. Li, Z. Chen and L. M. Fu, Molecules,
2017, 22, 1380.
There are no conflicts to declare.
22 C. Le Droumaguet, C. Wang and Q. Wang, Chem. Soc. Rev.,
2010, 39, 1233–1239.
23 V. Hong, S. I. Presolski, C. Ma and M. G. Finn, Angew. Chem.,
Int. Ed., 2009, 48, 9879–9883.
Acknowledgements
´
The participation of Leslie Bitard, Deborah Cardoso and
Sabine Boucheret (undergraduate students) is acknowledged.
The authors thank the Algerian Ministry of Higher Education
and Scientific Research, the Algerian Directorate General for
Scientific Research and Technological Development and the
French Ministry of Higher Education, Research and Innovation
for support of this work.
24 J. E. Moses and A. D. Moorhouse, Chem. Soc. Rev., 2007, 36,
1249–1262.
25 A. D. Becke, J. Chem. Phys., 1993, 98, 5648–5652.
26 P. J. Stephens, F. J. Devlin, C. F. Chabalowski and
M. J. Frisch, J. Phys. Chem., 1994, 98, 11623–11627.
27 P. C. Hariharan and J. A. Pople, Theor. Chim. Acta, 1973, 28,
213–222.
28 M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria,
M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone,
G. A. Petersson, H. Nakatsuji, X. Li, M. Caricato,
A. Marenich, J. Bloino, B. G. Janesko, R. Gomperts,
B. Mennucci, H. P. Hratchian, J. V. Ortiz, A. F. Izmaylov,
J. L. Sonnenberg, D. Williams-Young, F. Ding, F. Lipparini,
F. Egidi, J. Goings, B. Peng, A. Petrone, T. Henderson,
D. Ranasinghe, V. G. Zakrzewski, J. Gao, N. Rega,
G. Zheng, W. Liang, M. Hada, M. Ehara, K. Toyota,
R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima,
Y. Honda, O. Kitao, H. Nakai, T. Vreven, K. Throssell, J. A.
Montgomery, Jr., J. E. Peralta, F. Ogliaro, M. Bearpark,
J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staroverov,
T. Keith, R. Kobayashi, J. Normand, K. Raghavachari,
A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, M. Cossi,
J. M. Millam, M. Klene, C. Adamo, R. Cammi, J. W.
Ochterski, R. L. Martin, K. Morokuma, O. Farkas, J. B.
Foresman and D. J. Fox, Gaussian 09, Revision E.01,
Gaussian, Inc., Wallingford, CT, 2009.
References
1 M. D. Heagy, in Chemosensors: Principles, Strategies, and Applica-
tions, ed. B. Wang and E. V. Anslyn., 2011, pp. 253–273.
2 T. Ueno and T. Nagano, Nat. Methods, 2011, 8, 642–645.
3 H. Kobayashi, M. Ogawa, R. Alford, P. L. Choyke and Y. Urano,
Chem. Rev., 2009, 110, 2620–2640.
4 A. Martin, C. Long, R. J. Forster and T. E. Keyes, Chem.
Commun., 2012, 48, 5617.
5 M. Sameiro and T. Gonçalves, Chem. Rev., 2009, 109, 190–212.
´
6 K. Fauche, L. Nauton, L. Jouffret, F. Cisnetti and A. Gautier,
Chem. Commun., 2017, 53, 2402–2405.
7 C. Gibard, H. Ibrahim, A. Gautier and F. Cisnetti, Organo-
metallics, 2013, 32, 4279–4283.
8 D. Schweinfurth, L. Hettmanczyk, L. Suntrup and B. Sarkar,
Z. Anorg. Allg. Chem., 2017, 643, 554–584.
9 V. A. Chuiguk and A. G. Maidannik, Khim. Geterocikl. Soedin.,
1980, 1695–1696.
´
10 A. Messmer and A. Gelleri, Angew. Chem., Int. Ed., 1967, 6,
29 G. Scalmani, M. J. Frisch, B. Mennucci, J. Tomasi, R. Cammi
and V. Barone, J. Chem. Phys., 2006, 124, 094107.
30 M. E. Casida, C. Jamorski, K. C. Casida and D. R. Salahub,
J. Chem. Phys., 1998, 108, 4439–4449.
31 D. B. Ramachary, A. B. Shashank and S. Karthik, Angew.
Chem., Int. Ed., 2014, 53, 10420–10424.
261–262.
11 A. Mera, M. Ito, A. Nakayama and K. Namba, Chem. Lett.,
2017, 46, 539–542.
12 K. Namba, A. Mera, A. Osawa, E. Sakuda, N. Kitamura and
K. Tanino, Org. Lett., 2012, 14, 5554–5557.
13 T. Hayashi, A. Osawa, T. Watanabe, Y. Murata, A. Nakayama
and K. Namba, Tetrahedron Lett., 2017, 58, 1961–1964.
14 J. Sawada, A. Osawa, T. Takeuchi, M. Kaneda, S. Oishi, N. Fujii,
A. Asai, K. Tanino and K. Namba, Bioorg. Med. Chem. Lett., 2016,
26, 5765–5769.
¨
32 S. Brase, C. Gil, K. Knepper and V. Zimmermann, Angew.
Chem., Int. Ed., 2005, 44, 5188–5240.
33 K. A. Dururgkar, R. G. Gonnade and C. V. Ramana, Tetra-
hedron, 2009, 65, 3974–3979.
34 P. B. Ghosh, B. Ternai and M. W. Whitehouse, J. Med.
Chem., 1972, 15, 255–260.
35 D. Cantillo, M. Baghbanzadeh and C. O. Kappe, Angew.
Chem., Int. Ed., 2012, 51, 10190–10193.
36 H. Jian and J. M. Tour, J. Org. Chem., 2003, 68, 5091–5103.
37 K. Barral, A. D. Moorhouse and J. E. Moses, Org. Lett., 2007,
9, 1809–1811.
15 K. Namba, A. Osawa, A. Nakayama, A. Mera, F. Tano,
Y. Chuman, E. Sakuda, T. Taketsugu, K. Sakaguchi,
N. Kitamura and K. Tanino, Chem. Sci., 2015, 6, 1083–1093.
16 R. Cai, D. Wang, Y. Chen, W. Yan, N. R. Geise, S. Sharma,
H. Li, J. L. Petersen, M. Li and X. Shi, Chem. Commun., 2014,
50, 7303–7305.
17 B. Verbelen and W. Dehaen, Org. Lett., 2016, 18,
6412–6415.
38 H. Meerwein, Org. Synth., 1966, 46, 113.
18978 | New J. Chem., 2018, 42, 18969--18978 This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2018