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Green Chemistry
Page 6 of 8
DOI: 10.1039/C7GC02967E
COMMUNICATION
Journal Name
Commun., 2010, 46, 1813. (d)
and D. G. Hall, J. Org. Chem., 2012, 77, 8386–8400. (e) R. M.
N. Gernigon, R. M. Al-Zoubi
Green Chem., 2015, 17, 5140–5143. (d) C. Chen, F. Verpoort
and Q. Wu, RSC Adv., 2016, , 55599–55607.
Lanigan, P. Starkov and T. D. Sheppard, J. Org. Chem., 2013, 19 (a) F. Secci, A. Frongia, M. G. Rubanu, M. L. Sechi, G. Sarais,
6
78, 4512–4523. (f) C. Wang, H.-Z. Yu, Y. Fu and Q.-X. Guo,
Org. Biomol. Chem., 2013. (g) T. Mohy El Dine, W. Erb, Y.
M. Arca and P. P. Piras, European J. Org. Chem., 2014, 2014,
6659–6675. (b) F. Secci, M. Arca, A. Frongia and P. P. Piras,
New J. Chem., 2014, 38, 3622. (c) F. Secci, A. Frongia and P.
P. Piras, Tetrahedron Lett., 2014, 55, 603–605. (d) F. Secci,
M. Arca, A. Frongia and P. P. Piras, Catal. Sci. Technol., 2014,
Berhault, J. Rouden and J. Blanchet, J. Org. Chem., 2015, 80
4532–4544.
,
11 (a) J. Coste, D. Le-Nguyen and B. Castro, Tetrahedron Lett.,
1990, 31, 205–208. (b) J. Klose, A. El-Faham, P. Henklein, L. A.
Carpino and M. Bienert, Tetrahedron Lett., 1999, 40, 2045–
2048. (c) L. A. Carpino, J. Xia, C. Zhang and A. El-Faham, J.
Org. Chem., 2004, 69, 62–71.
12 (a) L. A. Carpino, H. Imazumi, A. El-Faham, F. J. Ferrer, C.
Zhang, Y. Lee, B. M. Foxman, P. Henklein, C. Hanay, C.
Mügge, H. Wenschuh, J. Klose, M. Beyermann and M. 20 (a) C. Cara, A. Musinu, V. Mameli, A. Ardu, D. Niznansky, J.
4
, 1407. (e) N. Melis, L. Ghisu, R. Guillot, P. Caboni, F. Secci,
D. J. Aitken and A. Frongia, European J. Org. Chem., 2015,
2015, 4358–4366. (f) N. Melis, F. Secci, T. Boddaert, D. J.
Aitken and A. Frongia, Chem. Commun., 2015, 51, 15272–
15275. (g) A. F. Vaquer, A. Frongia, F. Secci and E. Tuveri, RSC
Adv., 2015, 5, 96695–96704.
Bienert, Angew. Chemie Int. Ed., 2002, 41, 441–445. (b) O.
Marder, Y. Shvo and F. Albericio, ChemInform, 2003, 34
Bursik, M. A. Scorciapino, G. Manzo and C. Cannas, Cryst.
Growth Des., 2015, 15, 2364–2372. (b) M. Sanna Angotzi, A.
Musinu, V. Mameli, A. Ardu, C. Cara, D. Niznansky, H. L. Xin
and C. Cannas, ACS Nano, 2017, 11, 7889–7900. (c) M. A.
Scorciapino, R. Sanna, A. Ardu, F. Orrù, M. Casu, A. Musinu
and C. Cannas, J. Colloid Interface Sci., 2013, 407, 67–75. (d)
C. Cannas, A. Ardu, A. Musinu, L. Suber, G. Ciasca, H.
.
13 (a) C. Schotten, Berichte der Dtsch. Chem. Gesellschaft, 1884,
17, 2544–2547. (b) E. Baumann, Berichte der Dtsch. Chem.
Gesellschaft, 1886, 19, 3218–3222. (c) L. Zhang, X. Wang, J.
Wang, N. Grinberg, D. Krishnamurthy and C. H. Senanayake,
Tetrahedron Lett., 2009, 50, 2964–2966. (d) T. V Nguyen and
D. J. M. Lyons, Chem. Commun., 2015, 51, 3131–3134. (e) L.
Jiang, J. Yu, F. Niu, D. Zhang and X. Sun, Heteroat. Chem.,
2017, 28, e21364.
14 (a) J. Li, K. Subramaniam, D. Smith, J. X. Qiao, J. J. Li, J. Qian-
Cutrone, J. F. Kadow, G. D. Vite and B.-C. Chen, Org. Lett.,
2012, 14, 214–217. (b) F. Tinnis, H. Lundberg, T. Kivijärvi and
H. Adolfsson, in Organic Syntheses, John Wiley & Sons, Inc.,
Hoboken, NJ, USA, 2016, pp. 227–236.
Amenitsch and G. Campi, ACS Nano, 2015, 9, 7277–7286. (e)
S. Sun and H. Zeng, J. Am. Chem. Soc., 2002, 124, 8204–8205.
(f) Y. Hou, J. Yu and S. Gao, J. Mater. Chem., 2003, 13, 1983–
1987. (g) S. Sun, H. Zeng, D. B. Robinson, S. Raoux, P. M. Rice,
S. X. Wang and G. Li, J. Am. Chem. Soc., 2004, 126, 273–279.
(h) C. Dinh, T. Nguyen, F. Kleitz and T. Do, ACS Nano, 2009, 3,
3737–3743. (i) C. Cannas, A. Musinu, A. Ardu, F. Orrù, D.
Peddis, M. Casu, R. Sanna, F. Angius, G. Diaz and G.
Piccaluga, Chem. Mater., 2010, 22, 3353–3361. (j) D. Peddis,
F. Orrù, A. Ardu, C. Cannas, A. Musinu and G. Piccaluga,
Chem. Mater., 2012, 24, 1062–1071. (k) D. Peddis, C. Cannas,
A. Musinu, A. Ardu, F. Orrù, D. Fiorani, S. Laureti, D. Rinaldi,
G. Muscas, G. Concas and G. Piccaluga, Chem. Mater., 2013,
25, 2005–2013. (l) S. Mourdikoudis and L. M. Liz-Marzán,
Chem. Mater., 2013, 25, 1465–1476. (m) G. Muscas, G.
Concas, C. Cannas, A. Musinu, A. Ardu, F. Orrù, D. Fiorani, S.
Laureti, D. Rinaldi, G. Piccaluga and D. Peddis, J. Phys. Chem.
C, 2013, 117, 23378–23384. (n) G. Muscas, N. Yaacoub, G.
Concas, F. Sayed, R. Sayed Hassan, J. M. Greneche, C.
Cannas, A. Musinu, V. Foglietti, S. Casciardi, C. Sangregorio
15 (a) A. Basha, M. Lipton and S. M. Weinreb, Tetrahedron Lett.,
1977, 18, 4171–4172. (b) B. Gnanaprakasam and D. Milstein,
J. Am. Chem. Soc., 2011, 133, 1682–1685. (c) V. M. de
Oliveira, R. Silva de Jesus, A. F. Gomes, F. C. Gozzo, A. P.
Umpierre, P. A. Z. Suarez, J. C. Rubim and B. A. D. Neto,
ChemCatChem, 2011,
Nguyen and J. Mecinović, Tetrahedron, 2015, 71, 5547–5553.
(e) S. A. Miller and N. E. Leadbeater, RSC Adv., 2015,
93248–93251. (f) C. G. McPherson, N. Caldwell, C. Jamieson,
I. Simpson and A. J. B. Watson, Org. Biomol. Chem., 2017, 15
3507–3518. (g) S. A. Miller and N. E. Leadbeater, RSC Adv.,
2015, , 93248–93251
16 (a) G.-L. Li, K. K.-Y. Kung and M.-K. Wong, Chem. Commun.,
2012, 48, 4112. (b) K. S. Goh and C.-H. Tan, RSC Adv., 2012,
5536. (c) R. Cadoni, A. Porcheddu, G. Giacomelli and L. De
Luca, Org. Lett., 2012, 14 5014–5017. (d) G. N.
Papadopoulos and C. G. Kokotos, J. Org. Chem., 2016, 81
3, 1911–1920. (d) D. C. Lenstra, D. T.
5,
,
5
and D. Peddis, Nanoscale, 2015,
7, 13576–13585. (o) V.
2,
Mameli, A. Musinu, A. Ardu, G. Ennas, D. Peddis, D.
Niznansky, C. Sangregorio, C. Innocenti, N. T. K. Thanh and C.
Cannas, Nanoscale, 2016, 8, 10124–10137.
,
,
21 (a) M. Chen, Y.-G. Feng, X. Wang, T.-C. Li, J.-Y. Zhang and D.-J.
Qian, Langmuir, 2007, 23, 5296–5304. (b) C. Shen, C. Hui, T.
Yang, C. Xiao, J. Tian, L. Bao, S. Chen, H. Ding and H. Gao,
Chem. Mater., 2008, 20, 6939–6944. (c) K. M. Nam, J. H.
Shim, H. Ki, S.-I. Choi, G. Lee, J. K. Jang, Y. Jo, M.-H. Jung, H.
Song and J. T. Park, Angew. Chemie Int. Ed., 2008, 47, 9504–
9508. (d) H. Zhang, J. Ding, G. Chow, M. Ran and J. Yi, Chem.
Mater., 2009, 21, 5222–5228. (e) K. Lee, S. W. Kang, S.-U.
Lee, K.-H. Park, Y. W. Lee and S. W. Han, ACS Appl. Mater.
7023–7028. (e) H. Yang, W. Hu, S. Deng, T. Wu, H. Cen, Y.
Chen, D. Zhang and B. Wang, New J. Chem., 2015, 39, 5912–
5915. (f) E. Sankari Devi, A. Alanthadka, A. Tamilselvi, S.
Nagarajan, V. Sridharan and C. U. Maheswari, Org. Biomol.
Chem., 2016, 14, 8228–8231. (g) T. Narendar Reddy, B.
Raktani, R. Perla, M. Ravinder, J. R. Vaidya and N. J. Babu,
New J. Chem., 2017, 41, 9203–9209.
17 (a) L. U. Nordstrøm, H. Vogt and R. Madsen, J. Am. Chem.
Soc., 2008, 130, 17672–17673. (b) L. Zhang, W. Wang, A.
Wang, Y. Cui, X. Yang, Y. Huang, X. Liu, W. Liu, J. Son, H. Oji 22 R. T. Williamson, J. R. Carney and W. H. Gerwick, J. Nat.
Interfaces, 2012, 4, 4208–4214.
and T. Zhang, Green Chem., 2013, 15, 2680. (c) S. Gaspa, A.
Porcheddu and L. De Luca, Org. Biomol. Chem., 2013, 11
3803–7. (d) S. L. Zultanski, J. Zhao and S. S. Stahl, J. Am.
Chem. Soc., 2016, 138 6416–6419. (e) J.-F. Soulé, H.
Prod., 2000, 63, 876–878.
,
23 (a) L. Aloe, A. Leon and R. Levi-Montalcini, Agents Actions,
1993, 39, C145–C147. (b) J. LoVerme, G. La Rana, R. Russo, A.
Calignano and D. Piomelli, Life Sci., 2005, 77, 1685–1698. (c)
,
Miyamura and S. Kobayashi, J. Am. Chem. Soc., 2011, 133
18550–18553.
18 (a) P.-C. Chiang, Y. Kim and J. W. Bode, Chem. Commun.,
2009, 4566. (b) T. Wang, L. Yuan, Z. Zhao, A. Shao, M. Gao, Y.
Huang, F. Xiong, H. Zhang and J. Zhao, Green Chem., 2015,
17, 2741–2744. (c) T. T. S. Lew, D. S. W. Lim and Y. Zhang,
,
D. M. Lambert and C. J. Fowler, J. Med. Chem., 2005, 48,
5059–5087. (d) Y.-S. Wang, R. Shrestha, A. Kilaru, W. Wiant,
B. J. Venables, K. D. Chapman and E. B. Blancaflor, Proc. Natl.
Acad. Sci., 2006, 103, 12197–12202. (e) B. Costa, F. Comelli,
I. Bettoni, M. Colleoni and G. Giagnoni, Pain, 2008, 139, 541–
550. (f) J. Keereetaweep, A. Kilaru, I. Feussner, B. J. Venables
and K. D. Chapman, FEBS Lett., 2010, 584, 3215–3222. (g) E.
6 | J. Name., 2012, 00, 1-3
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