NJC
Paper
¨
14 (a) C. F. Nising and S. Brase, Chem. Soc. Rev., 2012, 41, 988;
57 (10%), 54 (100%), 31 (20%); HRMS (ESI) for C12H17N3O3
(M + H)+: calculated 252.1343; found, 252.1343.
¨
(b) C. F. Nising and S. Brase, Chem. Soc. Rev., 2008, 37, 1218.
15 S.-H. Guo, S.-Z. Xing, S. Mao, Y.-R. Gao, W.-L. Chen and
Y.-Q. Wang, Tetrahedron Lett., 2014, 55, 6718.
16 H.-L. Liu, H.-F. Jiang and Y.-G. Wang, Chin. J. Chem., 2007,
25, 1023.
17 J. E. Murtagh, S. H. McCooey and S. J. Connon, Chem.
Commun., 2005, 227.
G
0.5 dendrimer (14). Amber-colored syrup (m = 4.51 g; yield =
75%) IR (neat) n = 3366, 1728, 1645, 1197 cmÀ1 1H NMR
;
(CDCl3, 400 MHz) d = 2.45 (18H, t), 2.56 (6H, t), 2.77 (12H, t),
3.31 (6H, m), 3.51 (4H, t), 3.62 (1H, m), 3.68 (18H, s), 3.72 (4H, t),
3.74 (2H, t), 6.86 (2H, s), 6.92 (1H, s); 13C NMR (CDCl3, 100 MHz)
d = 32.6, 36.9, 37, 37.2, 49.3, 51.7, 52.9, 53.0, 66.5, 67.6, 70.6, 77.9,
171, 171.2, 173.0; HRMS (ESI) for C42H74N6O18 (M + H)+: calcu-
lated 951.5132; found, 951.5134.
18 F. Wang, H. Yang, H. Fu and Z. Pei, Chem. Commun., 2013,
49, 517.
19 C. Munro-Leighton, S. A. Delp, E. D. Blue and T. B. Gunnoe,
Organometallics, 2007, 26, 1483.
20 H. Guo, X. Li, J.-L. Wang, X.-H. Jin and X.-F. Lin, Tetrahedron,
2010, 66, 8300.
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