-
7
-
-
73249136665
-
-
T. Ben H. Ren S. Q. Ma D. P. Cao J. H. Lan X. F. Jing W. C. Wang J. Xu F. Deng J. M. Simmons S. L. Qiu G. S. Zhu Angew. Chem., Int. Ed. 2009 48 9457
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 9457
-
-
Ben, T.1
Ren, H.2
Ma, S.Q.3
Cao, D.P.4
Lan, J.H.5
Jing, X.F.6
Wang, W.C.7
Xu, J.8
Deng, F.9
Simmons, J.M.10
Qiu, S.L.11
Zhu, G.S.12
-
8
-
-
79959807223
-
-
p. 6822
-
R. Short, M. Carta, C. G. Bezzu, D. Fritsch, B. M. Kariuki and N. B. McKeown, Chem. Commun., 47, p. 6822
-
Chem. Commun.
, vol.47
-
-
Short, R.1
Carta, M.2
Bezzu, C.G.3
Fritsch, D.4
Kariuki, B.M.5
McKeown, N.B.6
-
11
-
-
33646417896
-
-
N. B. McKeown B. Gahnem K. J. Msayib P. M. Budd C. E. Tattershall K. Mahmood S. Tan D. Book H. W. Langmi A. Walton Angew. Chem., Int. Ed. 2006 45 1804
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 1804
-
-
McKeown, N.B.1
Gahnem, B.2
Msayib, K.J.3
Budd, P.M.4
Tattershall, C.E.5
Mahmood, K.6
Tan, S.7
Book, D.8
Langmi, H.W.9
Walton, A.10
-
13
-
-
45549105931
-
-
J. X. Jiang F. Su A. Trewin C. D. Wood H. Niu J. T. A. Jones Y. Z. Khimyak A. I. Cooper J. Am. Chem. Soc. 2008 130 7710
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7710
-
-
Jiang, J.X.1
Su, F.2
Trewin, A.3
Wood, C.D.4
Niu, H.5
Jones, J.T.A.6
Khimyak, Y.Z.7
Cooper, A.I.8
-
17
-
-
51349127016
-
-
C. D. Wood B. Tan A. Trewin F. Su M. J. Rosseinsky D. Bradshaw Y. Sun L. Zhou A. I. Cooper Adv. Mater. 2008 20 1916
-
(2008)
Adv. Mater.
, vol.20
, pp. 1916
-
-
Wood, C.D.1
Tan, B.2
Trewin, A.3
Su, F.4
Rosseinsky, M.J.5
Bradshaw, D.6
Sun, Y.7
Zhou, L.8
Cooper, A.I.9
-
20
-
-
70549107963
-
-
T. Tozawa J. T. A. Jones S. I. Swamy S. Jiang D. J. Adams S. Shakespeare R. Clowes D. Bradshaw T. Hasell S. Y. Chong C. Tang S. Thompson J. Parker A. Trewin J. Bacsa A. M. Z. Slawin A. Steiner A. I. Cooper Nat. Mater. 2009 8 973
-
(2009)
Nat. Mater.
, vol.8
, pp. 973
-
-
Tozawa, T.1
Jones, J.T.A.2
Swamy, S.I.3
Jiang, S.4
Adams, D.J.5
Shakespeare, S.6
Clowes, R.7
Bradshaw, D.8
Hasell, T.9
Chong, S.Y.10
Tang, C.11
Thompson, S.12
Parker, J.13
Trewin, A.14
Bacsa, J.15
Slawin, A.M.Z.16
Steiner, A.17
Cooper, A.I.18
-
27
-
-
79960936234
-
-
P. Sozzani O. Plietzsch C. I. Schilling T. Grab S. L. Grage A. S. Ulrich A. Comotti T. Muller S. Brase New J. Chem. 2011 35 1577
-
(2011)
New J. Chem.
, vol.35
, pp. 1577
-
-
Sozzani, P.1
Plietzsch, O.2
Schilling, C.I.3
Grab, T.4
Grage, S.L.5
Ulrich, A.S.6
Comotti, A.7
Muller, T.8
Brase, S.9
-
28
-
-
77956642594
-
-
M. J. Rosseinsky S. I. Swamy J. Bacsa J. T. A. Jones K. C. Stylianou A. Steiner L. K. Ritchie T. Hasell J. A. Gould A. Laybourn Y. Z. Khimyak D. J. Adams A. I. Cooper J. Am. Chem. Soc. 2010 132 12773
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 12773
-
-
Rosseinsky, M.J.1
Swamy, S.I.2
Bacsa, J.3
Jones, J.T.A.4
Stylianou, K.C.5
Steiner, A.6
Ritchie, L.K.7
Hasell, T.8
Gould, J.A.9
Laybourn, A.10
Khimyak, Y.Z.11
Adams, D.J.12
Cooper, A.I.13
-
29
-
-
61849094168
-
-
We have obtained up to 50% conversion of bromo functional groups using 6.6 equiv. of linker L1 under conventional heating conditions (85°C, 24 h)
-
N. L. Campbell R. Clowes L. K. Ritchie A. I. Cooper Chem. Mater. 2009 21 204
-
(2009)
Chem. Mater.
, vol.21
, pp. 204
-
-
Campbell, N.L.1
Clowes, R.2
Ritchie, L.K.3
Cooper, A.I.4
|