Please do not adjust margins
New Journal of Chemistry
Page 6 of 7
ARTICLE
Soc., 2014, 136, 14389; (m) S. Cai, K. Yang and D. Z. Wang,
Journal Name
1
2
3
4
5
6
7
8
9, 1782; (f) H. Kim, T. Kim, D. G. Lee,DSO.I:W10..1R0o3Vh9ie/Cwan9ANdrtiJcC0le1.O9L8nel4ineGe,
Chem. Commun. 2014, 50, 9273.
Org. Lett., 2014, 16, 2606; (n) L. Song, L. Zhang, S. Luo and J.-
P. Cheng, Chem. – Eur. J., 2014, 20, 14231.
5
G. Pandey, S. Koley, R. Talukdar and P. K, Sahani Org. Lett., 21 The acyl chloride D was detected and characterized, see
2018, 20, 5861.
B. Mühldorf and R. Wolf, Chem. Cat. Chem., 2017, 9, 920.
A. Kumar, P. Kumar, A. K. Pathak, A. N. Chokkapu and S. L. 23 (a) J. Fang, Z.-K. Wang, A.-W. Wu, W.-G. Shen, G.-Z. Ao and F.
Jain, ChemistrySelect, 2017, 2, 3437.
supporting information.
6
7
22 M. A. Cismesia and T. P. Yoon, Chem. Sci., 2015, 6, 5426.
Liu, Chem. Commun., 2017, 53, 7638; (b) K. Kawaai, T.
Yamaguchi, E. Yamaguchi, S. Endo, N. Tada, A. Ikari and A.
Itoh, J. Org. Chem., 2018, 83, 1988.
9
8
9
Y. Zhang, Q. Xiao, Y. Bao, Y. Zhang, S. Bottle, S. Sarina, B.
Zhaorigetu and H. Zhu, J. Phys. Chem. C, 2014, 118, 19062.
R. A. Larson, P. L. Stackhouse and T. O. Crowley, Environ. Sci.
Tecn., 1992, 26, 1792.
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
10 (a) S. Gaspa, A. Porcheddu and L. De Luca, Adv. Synth. Cat.,
2016, 358, 154; (b) S. Gaspa, A. Porcheddu and L. De Luca,
Org. Lett., 2015, 17, 3666;
11 (a) S. Gaspa, I. Amura, A. Porcheddu and L. De Luca, New J.
Chem., 2017, 41, 931; (b) S. Gaspa, A. Porcheddu and L. De
Luca, Tetrahedron Lett., 2017, 58, 2533.
12 (a) G. F. Mendoca and M. C. S. de Mattos, Curr. Org. Synth.,
2013, 10, 820; (b) S. H. Combe, A. Hosseini, A. Parra and P. R.
Schreiner, J. Org. Chem. 2017, 82, 2407; (c) H. Yang, W. Hu,
S. Deng, T. Wu, H. Cen, Y. Chen, D. Zhang and B. Wang, New
J. Chem., 2015, 39, 5912; (d) I. Saidalimu, Y. Liang, K. Niina, K.
Tanagawa, N. Saito and N. Shibata Org. Chem. Front., 2019,
6, 1157; (e ) M.-W. Chen, Z.-S. Ye, Z.-P. Chen, B. Wu and Y.-G.
Zhou Org. Chem. Front., 2015, 2, 586.
13 (a) I. A. Yunus, C. Basheer and H. A. Al-Muallem, J. Environ.
Chem. Eng., 2016, 4, 2802; (b) I. Cohen, A. K. Mishra, G.
Parvari, R. Edrei, M. Dantus, Y. Eichen and A. M. Szpilman,
Chem. Commun., 2017, 53, 10128; (c) N. Zhou, Y. Cheng, J.
Xie and C. Zhu, Chem. Commun., 2017, 53, 10707; (d) M.
Meanwell, J. Lehmann, M. Eichenberger, R. E. Martin and R.
Britton, Chem. Commun., 2018, 54, 9985; (e) V. R. Battula, H.
Singh, S. Kumar, I. Bala, S. K. Pal and K. Kailasam, ACS Catal.,
2018, 8, 6751; (f) S. Monticelli, W. Holzer, T. Langer, A.
Roller, B. Olofsson, V. Pace, ChemSusChem, 2019, 12, 1147.
14 (a) B. König, Eur. J. Org. Chem., 2017, 15, 1979; (b) M.
Oelgemoller, Chem. Rev., 2016, 116, 9664; (c) J. Guerra, D.
Cantillo and C. O. Kappe, Catal. Sci. Technol., 2016, 6, 4695;
(d) S. Deshpande, B. Gadilohar, Y. Shinde, D. Pinjari, A. Pandit
and G. Shankarling, Solar Energy, 2015, 113, 332; (e) D.
Cantillo, C. Mateos, J.A. Rincon, O. De Frutos and C. O.
Kappe, Chem. Eur. J., 2015, 21, 12894; (f) L.-L. Mao and H.
Cong, ChemSusChem, 2017, 10, 4461; (g) H. Yi, X. Hu, C. Bian
and A. Lei, ChemSusChem, 2017, 10, 79.
15 S. Protti, D. Ravelli, M. Fagnoni and A. Albini, Chem.
Commun., 2009, 7351.
16 The procedure was tested with 4-methoxybenzaldehyde and
4-aminobenzaldehyde but the corresponding acyl chlorides
were not detected.
17 (a) M. A. Ogliaruso and J. F. Wolfe, Synthesis of Carboxylic
Acids, Esters, and Their Derivatives, Wiley: New York, 1991,
p. 198; (b) M. A. Ogliaruso, J. F. Wolfe and D. S. Tarbell, Acc.
Chem. Res., 1969, 2, 296; (c) J. Rebek and D. Feitler, J. Am.
Chem. Soc., 1974, 96, 1606.
18 M. Konieczynska, C. Dai and C. R. J. Stephenson, Org.
Biomol. Chem., 2012, 10, 4509.
19 (a) D. Leow, Org. Lett., 2014, 16, 5812; (b) X.-F- Wang, S.-S.
Yu, C. Wang, D. Xue and J. Xiao, Org. Biomol. Chem., 2016,
14, 7028; (c) N. Iqbal and E. J. Cho, J. Org. Chem., 2016, 81,
1905; (d) L. Wang, M. Yu, C. Wu, N. Deng, C. Wang, X. Yao,
Adv. Synth. Catal., 2016, 358, 2631.
20 (a) A. L. J. Beckwith and J. E. Goodrich, Aust. J. Chem., 1965,
18, 747; (b) C. L. Hawkins and M. J. Davies, Chem. Res.
Toxicol., 2002, 15, 83; (c) W. Zhang, Y. Su. K.-H. Wang, L. Wu,
B. Chang, Y. Shi, D. Huang and Y. Hu, Org. Lett., 2017, 19,
376; (d) M. A. Short, J. M. Blackburn and J. L. Roizen, Angew.
Chem. Int. Ed., 2018, 57, 296; Angew. Chem., 2018, 130, 302
6 | J. Name., 2012, 00, 1-3
This journal is © The Royal Society of Chemistry 20xx
Please do not adjust margins