-
1
-
-
51649102031
-
Click chemistry, a powerful tool for pharmaceutical sciences
-
C.D. Hein, X.-M. Liu, and D. Wang Click chemistry, a powerful tool for pharmaceutical sciences Pharm. Res. 25 2008 2216 2230 10.1007/s11095-008-9616-1
-
(2008)
Pharm. Res.
, vol.25
, pp. 2216-2230
-
-
Hein, C.D.1
Liu, X.-M.2
Wang, D.3
-
2
-
-
81255143206
-
Regenerative biomaterials that "click": Simple, aqueous-based protocols for hydrogel synthesis, surface immobilization, and 3D patterning
-
C.M. Nimmo, and M.S. Shoichet Regenerative biomaterials that "click": simple, aqueous-based protocols for hydrogel synthesis, surface immobilization, and 3D patterning Bioconjugate Chem. 22 2011 2199 2209 10.1021/bc200281k
-
(2011)
Bioconjugate Chem.
, vol.22
, pp. 2199-2209
-
-
Nimmo, C.M.1
Shoichet, M.S.2
-
3
-
-
84860577785
-
Click chemistry for drug delivery nanosystems
-
E. Lallana, A. Sousa-Herves, F. Fernandez-Trillo, R. Riguera, and E. Fernandez-Megia Click chemistry for drug delivery nanosystems Pharm. Res. 29 2011 1 34 10.1007/s11095-011-0568-5
-
(2011)
Pharm. Res.
, vol.29
, pp. 1-34
-
-
Lallana, E.1
Sousa-Herves, A.2
Fernandez-Trillo, F.3
Riguera, R.4
Fernandez-Megia, E.5
-
4
-
-
84862696152
-
Click chemistry with polymers, dendrimers, and hydrogels for drug delivery
-
E. Lallana, F. Fernandez-Trillo, A. Sousa-Herves, R. Riguera, and E. Fernandez-Megia Click chemistry with polymers, dendrimers, and hydrogels for drug delivery Pharm. Res. 29 2012 902 921 10.1007/s11095-012-0683-y
-
(2012)
Pharm. Res.
, vol.29
, pp. 902-921
-
-
Lallana, E.1
Fernandez-Trillo, F.2
Sousa-Herves, A.3
Riguera, R.4
Fernandez-Megia, E.5
-
5
-
-
84910015748
-
Click chemistry in complex mixtures: Bioorthogonal bioconjugation
-
C.S. McKay, and M.G. Finn Click chemistry in complex mixtures: bioorthogonal bioconjugation Chem. Biol. 21 2014 1075 1101 10.1016/j.chembiol.2014.09.002
-
(2014)
Chem. Biol.
, vol.21
, pp. 1075-1101
-
-
McKay, C.S.1
Finn, M.G.2
-
6
-
-
0000096835
-
Click chemistry: Diverse chemical function from a few good reactions
-
H.C. Kolb, M.G. Finn, and K.B. Sharpless Click chemistry: diverse chemical function from a few good reactions Angew. Chem. Int. Ed. 40 2001 2004 2021 10.1002/1521-3773(20010601)40:11<2004::AID-ANIE2004>3.0.CO;2-5
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
7
-
-
0348109450
-
The growing impact of click chemistry on drug discovery
-
H.C. Kolb, and K.B. Sharpless The growing impact of click chemistry on drug discovery Drug Discov. Today 8 2003 1128 1137 10.1016/S1359-6446(03)02933-7
-
(2003)
Drug Discov. Today
, vol.8
, pp. 1128-1137
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
8
-
-
34547272503
-
The growing applications of click chemistry
-
J.E. Moses, and A.D. Moorhouse The growing applications of click chemistry Chem. Soc. Rev. 36 2007 1249 1262 10.1039/b613014n
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1249-1262
-
-
Moses, J.E.1
Moorhouse, A.D.2
-
9
-
-
33846703461
-
"click" chemistry in polymer and materials science
-
W.H. Binder, and R. Sachsenhofer "Click" chemistry in polymer and materials science Macromol. Rapid Commun. 28 2007 15 54 10.1002/marc.200600625
-
(2007)
Macromol. Rapid Commun.
, vol.28
, pp. 15-54
-
-
Binder, W.H.1
Sachsenhofer, R.2
-
10
-
-
54749104711
-
"click" chemistry in polymer and material science. An update
-
W.H. Binder, and R. Sachsenhofer "Click" chemistry in polymer and material science. An update Macromol. Rapid Commun. 29 2008 952 981 10.1002/marc.200800089
-
(2008)
Macromol. Rapid Commun.
, vol.29
, pp. 952-981
-
-
Binder, W.H.1
Sachsenhofer, R.2
-
11
-
-
73649085447
-
Macromolecular engineering through click chemistry and other efficient transformations
-
B.S. Sumerlin, and A.P. Vogt Macromolecular engineering through click chemistry and other efficient transformations Macromolecules 43 2010 1 13 10.1021/ma901447e
-
(2010)
Macromolecules
, vol.43
, pp. 1-13
-
-
Sumerlin, B.S.1
Vogt, A.P.2
-
12
-
-
77949812304
-
Marrying click chemistry with polymerization: Expanding the scope of polymeric materials
-
P.L. Golas, and K. Matyjaszewski Marrying click chemistry with polymerization: expanding the scope of polymeric materials Chem. Soc. Rev. 39 2010 1338 1354 10.1039/B901978M
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1338-1354
-
-
Golas, P.L.1
Matyjaszewski, K.2
-
13
-
-
0037012920
-
Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
-
C.W. Tornøe, C. Christensen, and M. Meldal Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides J. Org. Chem. 67 2002 3057 3064 10.1021/jo011148j
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3057-3064
-
-
Tornøe, C.W.1
Christensen, C.2
Meldal, M.3
-
14
-
-
0037099395
-
A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
V.V. Rostovtsev, L.G. Green, V.V. Fokin, and K.B. Sharpless A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes Angew. Chem. Int. Ed. 41 2002 2596 2599 10.1002/1521-3773(20020715)41:14<2596::AID-ANIE2596>3.0.CO;2-4
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
15
-
-
77949863611
-
Cu-free click cycloaddition reactions in chemical biology
-
J.C. Jewett, and C.R. Bertozzi Cu-free click cycloaddition reactions in chemical biology Chem. Soc. Rev. 39 2010 1272 1279 10.1039/B901970G
-
(2010)
Chem. Soc. Rev.
, vol.39
, pp. 1272-1279
-
-
Jewett, J.C.1
Bertozzi, C.R.2
-
16
-
-
9344227358
-
A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems
-
N.J. Agard, J.A. Prescher, and C.R. Bertozzi A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems J. Am. Chem. Soc. 126 2004 15046 15047 10.1021/ja044996f
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15046-15047
-
-
Agard, N.J.1
Prescher, J.A.2
Bertozzi, C.R.3
-
17
-
-
50249085119
-
Second-generation difluorinated cyclooctynes for copper-free click chemistry
-
J.A. Codelli, J.M. Baskin, N.J. Agard, and C.R. Bertozzi Second-generation difluorinated cyclooctynes for copper-free click chemistry J. Am. Chem. Soc. 130 2008 11486 11493 10.1021/ja803086r
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 11486-11493
-
-
Codelli, J.A.1
Baskin, J.M.2
Agard, N.J.3
Bertozzi, C.R.4
-
18
-
-
70349769688
-
Click chemistry beyond metal-catalyzed cycloaddition
-
C.R. Becer, R. Hoogenboom, and U.S. Schubert Click chemistry beyond metal-catalyzed cycloaddition Angew. Chem. Int. Ed. 48 2009 4900 4908 10.1002/anie.200900755
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 4900-4908
-
-
Becer, C.R.1
Hoogenboom, R.2
Schubert, U.S.3
-
19
-
-
77954308974
-
Diels-Alder cycloaddition-cycloreversion: A powerful combo in materials design
-
A. Sanyal Diels-Alder cycloaddition-cycloreversion: a powerful combo in materials design Macromol. Chem. Phys. 211 2010 1417 1425 10.1002/macp.201000108
-
(2010)
Macromol. Chem. Phys.
, vol.211
, pp. 1417-1425
-
-
Sanyal, A.1
-
20
-
-
80052757487
-
Diels-Alder "click" reactions: Recent applications in polymer and material science
-
M.A. Tasdelen Diels-Alder "click" reactions: recent applications in polymer and material science Polym. Chem. 2 2011 2133 2145 10.1039/c1py00041a
-
(2011)
Polym. Chem.
, vol.2
, pp. 2133-2145
-
-
Tasdelen, M.A.1
-
21
-
-
84873991048
-
The furan/maleimide Diels-Alder reaction: A versatile click-unclick tool in macromolecular synthesis
-
A. Gandini The furan/maleimide Diels-Alder reaction: a versatile click-unclick tool in macromolecular synthesis Prog. Polym. Sci. 38 2013 1 29 10.1016/j.progpolymsci.2012.04.002
-
(2013)
Prog. Polym. Sci.
, vol.38
, pp. 1-29
-
-
Gandini, A.1
-
22
-
-
33947480910
-
Acceleration of the Diels-Alder reaction by aluminum chloride
-
P. Yates, and P. Eaton Acceleration of the Diels-Alder reaction by aluminum chloride J. Am. Chem. Soc. 82 1960 4436 4437 10.1021/ja01501a085
-
(1960)
J. Am. Chem. Soc.
, vol.82
, pp. 4436-4437
-
-
Yates, P.1
Eaton, P.2
-
23
-
-
0000555145
-
Catalytic actions of aluminum chloride on the isoprene - Methyl acrylate Diels-Alder reaction
-
T. Inukai, and T. Kojima Catalytic actions of aluminum chloride on the isoprene - methyl acrylate Diels-Alder reaction J. Org. Chem. 31 1966 1121 1123 10.1021/jo01342a031
-
(1966)
J. Org. Chem.
, vol.31
, pp. 1121-1123
-
-
Inukai, T.1
Kojima, T.2
-
24
-
-
0028933767
-
Lewis-acid catalysis of a Diels-Alder reaction in water
-
S. Otto, and J.B.F.N. Engberts Lewis-acid catalysis of a Diels-Alder reaction in water Tetrahedron Lett. 36 1995 2645 2648 10.1016/0040-4039(95)00304-U
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 2645-2648
-
-
Otto, S.1
Engberts, J.B.F.N.2
-
25
-
-
0029813957
-
Lewis acid catalysis of a Diels-Alder reaction in water
-
S. Otto, F. Bertoncin, and J.B.F.N. Engberts Lewis acid catalysis of a Diels-Alder reaction in water J. Am. Chem. Soc. 118 1996 7702 7707 10.1021/ja960318k
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 7702-7707
-
-
Otto, S.1
Bertoncin, F.2
Engberts, J.B.F.N.3
-
26
-
-
84962105974
-
Synthesen in der hydroaromatischen Reihe, I. Mitteilung: Anlagerung von "di-en"-kohlenwasserstoffen
-
O. Diels, and K. Alder Synthesen in der hydroaromatischen Reihe, I. Mitteilung: Anlagerung von "Di-en"-kohlenwasserstoffen Justus Liebigs Ann. Chem. 460 1928 98 122 10.1002/jlac.19284600106
-
(1928)
Justus Liebigs Ann. Chem.
, vol.460
, pp. 98-122
-
-
Diels, O.1
Alder, K.2
-
27
-
-
85178443214
-
Synthesen in der hydro-aromatischen Reihe, II. Mitteilung: Über Cantharidin
-
O. Diels, and K. Alder Synthesen in der hydro-aromatischen Reihe, II. Mitteilung: Über Cantharidin Ber. Dtsch. Chem. Ges. a/B. 62 1929 554 562 10.1002/cber.19290620318
-
(1929)
Ber. Dtsch. Chem. Ges. A/B.
, vol.62
, pp. 554-562
-
-
Diels, O.1
Alder, K.2
-
29
-
-
33947450396
-
The total synthesis of steroids
-
R.B. Woodward, F. Sondheimer, D. Taub, K. Heusler, and W.M. McLamore The total synthesis of steroids J. Am. Chem. Soc. 74 1952 4223 4251 10.1021/ja01137a001
-
(1952)
J. Am. Chem. Soc.
, vol.74
, pp. 4223-4251
-
-
Woodward, R.B.1
Sondheimer, F.2
Taub, D.3
Heusler, K.4
McLamore, W.M.5
-
30
-
-
33947457625
-
The synthesis of morphine
-
M. Gates, and G. Tschudi The synthesis of morphine J. Am. Chem. Soc. 74 1952 1109 1110 10.1021/ja01124a538
-
(1952)
J. Am. Chem. Soc.
, vol.74
, pp. 1109-1110
-
-
Gates, M.1
Tschudi, G.2
-
31
-
-
33947469818
-
The synthesis of morphine
-
M. Gates, and G. Tschudi The synthesis of morphine J. Am. Chem. Soc. 78 1956 1380 1393 10.1021/ja01588a033
-
(1956)
J. Am. Chem. Soc.
, vol.78
, pp. 1380-1393
-
-
Gates, M.1
Tschudi, G.2
-
32
-
-
0002616937
-
The mechanism of the Diels-Alder reaction
-
R.B. Woodward, and T.J. Katz The mechanism of the Diels-Alder reaction Tetrahedron 5 1959 70 89 10.1016/0040-4020(59)80072-7
-
(1959)
Tetrahedron
, vol.5
, pp. 70-89
-
-
Woodward, R.B.1
Katz, T.J.2
-
33
-
-
84981778017
-
The conservation of orbital symmetry
-
R.B. Woodward, and R. Hoffmann The conservation of orbital symmetry Angew. Chem. Int. Ed. 8 1969 781 853 10.1002/anie.196907811
-
(1969)
Angew. Chem. Int. Ed.
, vol.8
, pp. 781-853
-
-
Woodward, R.B.1
Hoffmann, R.2
-
34
-
-
0342713055
-
Mechanistic aspects of Diels-Alder reactions: A critical survey
-
J. Sauer, and R. Sustmann Mechanistic aspects of Diels-Alder reactions: a critical survey Angew. Chem. Int. Ed. 19 1980 779 807 10.1002/anie.198007791
-
(1980)
Angew. Chem. Int. Ed.
, vol.19
, pp. 779-807
-
-
Sauer, J.1
Sustmann, R.2
-
35
-
-
33845374957
-
Evidence for the concerted mechanism of the Diels-Alder reaction of butadiene with ethylene
-
K.N. Houk, Y.T. Lin, and F.K. Brown Evidence for the concerted mechanism of the Diels-Alder reaction of butadiene with ethylene J. Am. Chem. Soc. 108 1986 554 556 10.1021/ja00263a059
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 554-556
-
-
Houk, K.N.1
Lin, Y.T.2
Brown, F.K.3
-
36
-
-
33845374838
-
Mechanism of the Diels-Alder reaction: Reactions of butadiene with ethylene and cyanoethylenes
-
M.J.S. Dewar, S. Olivella, and J.J.P. Stewart Mechanism of the Diels-Alder reaction: reactions of butadiene with ethylene and cyanoethylenes J. Am. Chem. Soc. 108 1986 5771 5779 10.1021/ja00279a018
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 5771-5779
-
-
Dewar, M.J.S.1
Olivella, S.2
Stewart, J.J.P.3
-
37
-
-
0001754618
-
Untersuchungen über den Verlauf der Diensynthese
-
K. Alder, and G. Stein Untersuchungen über den Verlauf der Diensynthese Angew. Chem. 50 1937 510 519 10.1002/ange.19370502804
-
(1937)
Angew. Chem.
, vol.50
, pp. 510-519
-
-
Alder, K.1
Stein, G.2
-
38
-
-
0001741781
-
Orbital symmetries and endo-exo relationships in concerted cycloaddition reactions
-
R. Hoffmann, and R.B. Woodward Orbital symmetries and endo-exo relationships in concerted cycloaddition reactions J. Am. Chem. Soc. 87 1965 4388 4389 10.1021/ja00947a033
-
(1965)
J. Am. Chem. Soc.
, vol.87
, pp. 4388-4389
-
-
Hoffmann, R.1
Woodward, R.B.2
-
39
-
-
0028518279
-
Thermoreversible reaction of Diels-Alder polymer composed of difurufuryladipate with bismaleimidodiphenylmethane
-
N. Kuramoto, K. Hayashi, and K. Nagai Thermoreversible reaction of Diels-Alder polymer composed of difurufuryladipate with bismaleimidodiphenylmethane J. Polym. Sci. A: Polym. Chem. 32 1994 2501 2504 10.1002/pola.1994.080321312
-
(1994)
J. Polym. Sci. A: Polym. Chem.
, vol.32
, pp. 2501-2504
-
-
Kuramoto, N.1
Hayashi, K.2
Nagai, K.3
-
40
-
-
0020842464
-
Synthesis, characterization, and Diels-Alder extension of cyclopentadiene telechelic polyisobutylene. III. Silylcyclopentadiene-telechelic polyisobutylene
-
J.P. Kennedy, and G.M. Carlson Synthesis, characterization, and Diels-Alder extension of cyclopentadiene telechelic polyisobutylene. III. Silylcyclopentadiene-telechelic polyisobutylene J. Polym. Sci. Polym. Chem. Ed. 21 1983 2973 2986 10.1002/pol.1983.170211013
-
(1983)
J. Polym. Sci. Polym. Chem. Ed.
, vol.21
, pp. 2973-2986
-
-
Kennedy, J.P.1
Carlson, G.M.2
-
41
-
-
0020936596
-
Synthesis, characterization, and Diels-Alder extension of cyclopentadiene telechelic polyisobutylene. IV. α,ω-Di(3-cyclopentadienylpropyldimethylsilyl)polyisobutylene
-
J.P. Kennedy, and G.M. Carlson Synthesis, characterization, and Diels-Alder extension of cyclopentadiene telechelic polyisobutylene. IV. α,ω-Di(3-cyclopentadienylpropyldimethylsilyl)polyisobutylene J. Polym. Sci. Polym. Chem. Ed. 21 1983 3551 3561 10.1002/pol.1983.170211216
-
(1983)
J. Polym. Sci. Polym. Chem. Ed.
, vol.21
, pp. 3551-3561
-
-
Kennedy, J.P.1
Carlson, G.M.2
-
42
-
-
0027641554
-
A review of thermally controlled covalent bond formation in polymer chemistry
-
L.P. Engle, and K.B. Wagener A review of thermally controlled covalent bond formation in polymer chemistry J. Macromol. Sci. Polym. Rev. 33 1993 239 257 10.1080/15321799308021436
-
(1993)
J. Macromol. Sci. Polym. Rev.
, vol.33
, pp. 239-257
-
-
Engle, L.P.1
Wagener, K.B.2
-
43
-
-
84906084015
-
Kinetic studies of inverse electron demand Diels-Alder reactions (iEDDA) of norbornenes and 3,6-dipyridin-2-yl-1,2,4,5-tetrazine
-
A.-C. Knall, M. Hollauf, and C. Slugovc Kinetic studies of inverse electron demand Diels-Alder reactions (iEDDA) of norbornenes and 3,6-dipyridin-2-yl-1,2,4,5-tetrazine Tetrahedron Lett. 55 2014 4763 4766 10.1016/j.tetlet.2014.07.002
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 4763-4766
-
-
Knall, A.-C.1
Hollauf, M.2
Slugovc, C.3
-
44
-
-
33847085398
-
Hydrophobic acceleration of Diels-Alder reactions
-
D.C. Rideout, and R. Breslow Hydrophobic acceleration of Diels-Alder reactions J. Am. Chem. Soc. 102 1980 7816 7817 10.1021/ja00546a048
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 7816-7817
-
-
Rideout, D.C.1
Breslow, R.2
-
45
-
-
0001300546
-
Selective Diels-alder reactions in aqueous solutions and suspensions
-
R. Breslow, U. Maitra, and D. Rideout Selective Diels-alder reactions in aqueous solutions and suspensions Tetrahedron Lett. 24 1983 1901 1904 10.1016/S0040-4039(00)81801-8
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 1901-1904
-
-
Breslow, R.1
Maitra, U.2
Rideout, D.3
-
46
-
-
0000945578
-
Diels-Alder reactions in aqueous solutions. Enforced hydrophobic interactions between diene and dienophile
-
W. Blokzijl, M.J. Blandamer, and J.B.F.N. Engberts Diels-Alder reactions in aqueous solutions. Enforced hydrophobic interactions between diene and dienophile J. Am. Chem. Soc. 113 1991 4241 4246 10.1021/ja00011a029
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 4241-4246
-
-
Blokzijl, W.1
Blandamer, M.J.2
Engberts, J.B.F.N.3
-
47
-
-
0031763196
-
Effects of the hydrophobicity of the reactants on Diels-Alder reactions in water
-
A. Meijer, S. Otto, and J.B.F.N. Engberts Effects of the hydrophobicity of the reactants on Diels-Alder reactions in water J. Org. Chem. 63 1998 8989 8994 10.1021/jo981359x
-
(1998)
J. Org. Chem.
, vol.63
, pp. 8989-8994
-
-
Meijer, A.1
Otto, S.2
Engberts, J.B.F.N.3
-
48
-
-
29544450520
-
Diels-Alder ligation and surface immobilization of proteins
-
A.D. de Araújo, J.M. Palomo, J. Cramer, M. Köhn, H. Schröder, R. Wacker, and et al. Diels-Alder ligation and surface immobilization of proteins Angew. Chem. Int. Ed. 45 2006 296 301 10.1002/anie.200502266
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 296-301
-
-
De Araújo, A.D.1
Palomo, J.M.2
Cramer, J.3
Köhn, M.4
Schröder, H.5
Wacker, R.6
-
49
-
-
64549086668
-
Rheological and chemical analysis of reverse gelation in a covalently cross-linked Diels-Alder polymer network
-
B.J. Adzima, H.A. Aguirre, C.J. Kloxin, T.F. Scott, and C.N. Bowman Rheological and chemical analysis of reverse gelation in a covalently cross-linked Diels-Alder polymer network Macromolecules 41 2008 9112 9117 10.1021/ma801863d
-
(2008)
Macromolecules
, vol.41
, pp. 9112-9117
-
-
Adzima, B.J.1
Aguirre, H.A.2
Kloxin, C.J.3
Scott, T.F.4
Bowman, C.N.5
-
50
-
-
84872617032
-
A self-healing polymer network based on reversible covalent bonding
-
G. Scheltjens, M.M. Diaz, J. Brancart, G. Van Assche, and B. Van Mele A self-healing polymer network based on reversible covalent bonding React. Funct. Polym. 73 2013 413 420 10.1016/j.reactfunctpolym.2012.06.017
-
(2013)
React. Funct. Polym.
, vol.73
, pp. 413-420
-
-
Scheltjens, G.1
Diaz, M.M.2
Brancart, J.3
Van Assche, G.4
Van Mele, B.5
-
51
-
-
84867232741
-
Kinetic and thermodynamic measurements for the facile property prediction of Diels-Alder-conjugated material behavior
-
K.C. Koehler, A. Durackova, C.J. Kloxin, and C.N. Bowman Kinetic and thermodynamic measurements for the facile property prediction of Diels-Alder-conjugated material behavior AIChE J. 58 2012 3545 3552 10.1002/aic.13733
-
(2012)
AIChE J.
, vol.58
, pp. 3545-3552
-
-
Koehler, K.C.1
Durackova, A.2
Kloxin, C.J.3
Bowman, C.N.4
-
52
-
-
84961986609
-
Substituent effects on the reversibility of furan-maleimide cycloadditions
-
R.C. Boutelle, and B.H. Northrop Substituent effects on the reversibility of furan-maleimide cycloadditions J. Org. Chem. 76 2011 7994 8002 10.1021/jo201606z
-
(2011)
J. Org. Chem.
, vol.76
, pp. 7994-8002
-
-
Boutelle, R.C.1
Northrop, B.H.2
-
53
-
-
0027180686
-
Block copolymer micelles as vehicles for drug delivery
-
K. Kataoka, G.S. Kwon, M. Yokoyama, T. Okano, and Y. Sakurai Block copolymer micelles as vehicles for drug delivery J. Control. Release 24 1993 119 132 10.1016/0168-3659(93)90172-2
-
(1993)
J. Control. Release
, vol.24
, pp. 119-132
-
-
Kataoka, K.1
Kwon, G.S.2
Yokoyama, M.3
Okano, T.4
Sakurai, Y.5
-
54
-
-
0035937592
-
Block copolymer micelles for drug delivery: Design, characterization and biological significance
-
K. Kataoka, A. Harada, and Y. Nagasaki Block copolymer micelles for drug delivery: design, characterization and biological significance Adv. Drug Deliv. Rev. 47 2001 113 131 10.1016/S0169-409X(00)00124-1
-
(2001)
Adv. Drug Deliv. Rev.
, vol.47
, pp. 113-131
-
-
Kataoka, K.1
Harada, A.2
Nagasaki, Y.3
-
55
-
-
28544450961
-
Block copolymer micelles: Preparation, characterization and application in drug delivery
-
G. Gaucher, M.-H. Dufresne, V.P. Sant, N. Kang, D. Maysinger, and J.-C. Leroux Block copolymer micelles: preparation, characterization and application in drug delivery J. Control. Release 109 2005 169 188 10.1016/j.jconrel.2005.09.034
-
(2005)
J. Control. Release
, vol.109
, pp. 169-188
-
-
Gaucher, G.1
Dufresne, M.-H.2
Sant, V.P.3
Kang, N.4
Maysinger, D.5
Leroux, J.-C.6
-
56
-
-
84870255747
-
Advanced drug delivery devices via self-assembly of amphiphilic block copolymers
-
A. Rösler, G.W.M. Vandermeulen, and H.-A. Klok Advanced drug delivery devices via self-assembly of amphiphilic block copolymers Adv. Drug Deliv. Rev. 64 2012 270 279 10.1016/j.addr.2012.09.026
-
(2012)
Adv. Drug Deliv. Rev.
, vol.64
, pp. 270-279
-
-
Rösler, A.1
Vandermeulen, G.W.M.2
Klok, H.-A.3
-
57
-
-
0037148596
-
Pluronic® block copolymers: Novel functional molecules for gene therapy
-
A.V. Kabanov, P. Lemieux, S. Vinogradov, and V. Alakhov Pluronic® block copolymers: novel functional molecules for gene therapy Adv. Drug Deliv. Rev. 54 2002 223 233 10.1016/S0169-409X(02)00018-2
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 223-233
-
-
Kabanov, A.V.1
Lemieux, P.2
Vinogradov, S.3
Alakhov, V.4
-
58
-
-
55249114136
-
Amphiphilic block copolymers enhance cellular uptake and nuclear entry of polyplex-delivered DNA
-
Z. Yang, G. Sahay, S. Sriadibhatla, and A.V. Kabanov Amphiphilic block copolymers enhance cellular uptake and nuclear entry of polyplex-delivered DNA Bioconjugate Chem. 19 2008 1987 1994 10.1021/bc800144a
-
(2008)
Bioconjugate Chem.
, vol.19
, pp. 1987-1994
-
-
Yang, Z.1
Sahay, G.2
Sriadibhatla, S.3
Kabanov, A.V.4
-
59
-
-
0142248298
-
Nanostructure fabrication using block copolymers
-
I.W. Hamley Nanostructure fabrication using block copolymers Nanotechnology 14 2003 R39 R54 10.1088/0957-4484/14/10/201
-
(2003)
Nanotechnology
, vol.14
, pp. R39-R54
-
-
Hamley, I.W.1
-
60
-
-
33847256524
-
A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: Micelles, nanospheres, nanocapsules and polymersomes
-
K. Letchford, and H. Burt A review of the formation and classification of amphiphilic block copolymer nanoparticulate structures: micelles, nanospheres, nanocapsules and polymersomes Eur. J. Pharm. Biopharm. 65 2007 259 269 10.1016/j.ejpb.2006.11.009
-
(2007)
Eur. J. Pharm. Biopharm.
, vol.65
, pp. 259-269
-
-
Letchford, K.1
Burt, H.2
-
61
-
-
40649105534
-
Precise engineering of targeted nanoparticles by using self-assembled biointegrated block copolymers
-
F. Gu, L. Zhang, B.A. Teply, N. Mann, A. Wang, A.F. Radovic-Moreno, and et al. Precise engineering of targeted nanoparticles by using self-assembled biointegrated block copolymers Proc. Natl. Acad. Sci. U.S.A. 105 2008 2586 2591 10.1073/pnas.0711714105
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 2586-2591
-
-
Gu, F.1
Zhang, L.2
Teply, B.A.3
Mann, N.4
Wang, A.5
Radovic-Moreno, A.F.6
-
62
-
-
0024635932
-
Protein-resistant surfaces prepared by PEO-containing block copolymer surfactants
-
J.H. Lee, J. Kopecek, and J.D. Andrade Protein-resistant surfaces prepared by PEO-containing block copolymer surfactants J. Biomed. Mater. Res. 23 1989 351 368 10.1002/jbm.820230306
-
(1989)
J. Biomed. Mater. Res.
, vol.23
, pp. 351-368
-
-
Lee, J.H.1
Kopecek, J.2
Andrade, J.D.3
-
63
-
-
0027657696
-
Surface modification of nanoparticles by PEO/PPO block copolymers to minimize interactions with blood components and prolong blood circulation in rats
-
J.S. Tan, D.E. Butterfield, C.L. Voycheck, K.D. Caldwell, and J.T. Li Surface modification of nanoparticles by PEO/PPO block copolymers to minimize interactions with blood components and prolong blood circulation in rats Biomaterials 14 1993 823 833 10.1016/0142-9612(93)90004-L
-
(1993)
Biomaterials
, vol.14
, pp. 823-833
-
-
Tan, J.S.1
Butterfield, D.E.2
Voycheck, C.L.3
Caldwell, K.D.4
Li, J.T.5
-
64
-
-
0032642126
-
Coating of surfaces with stabilized reactive micelles from poly(ethylene glycol)-poly(DL-lactic acid) block copolymer
-
K. Emoto, Y. Nagasaki, and K. Kataoka Coating of surfaces with stabilized reactive micelles from poly(ethylene glycol)-poly(DL-lactic acid) block copolymer Langmuir 15 1999 5212 5218 10.1021/la980918s
-
(1999)
Langmuir
, vol.15
, pp. 5212-5218
-
-
Emoto, K.1
Nagasaki, Y.2
Kataoka, K.3
-
65
-
-
0001319478
-
Biodegradable block copolymers as injectable drug-delivery systems
-
B. Jeong, Y.H. Bae, D.S. Lee, and S.W. Kim Biodegradable block copolymers as injectable drug-delivery systems Nature 388 1997 860 862 10.1038/42218
-
(1997)
Nature
, vol.388
, pp. 860-862
-
-
Jeong, B.1
Bae, Y.H.2
Lee, D.S.3
Kim, S.W.4
-
66
-
-
47749146197
-
Injectable hydrogels as unique biomedical materials
-
L. Yu, and J. Ding Injectable hydrogels as unique biomedical materials Chem. Soc. Rev. 37 2008 1473 1481 10.1039/B713009K
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1473-1481
-
-
Yu, L.1
Ding, J.2
-
67
-
-
42049097246
-
In situ gelling stimuli-sensitive block copolymer hydrogels for drug delivery
-
C. He, S.W. Kim, and D.S. Lee In situ gelling stimuli-sensitive block copolymer hydrogels for drug delivery J. Control. Release 127 2008 189 207 10.1016/j.jconrel.2008.01.005
-
(2008)
J. Control. Release
, vol.127
, pp. 189-207
-
-
He, C.1
Kim, S.W.2
Lee, D.S.3
-
68
-
-
64249136171
-
Recyclable shape-memory polymer: Poly(lactic acid) crosslinked by a thermoreversible Diels-Alder reaction
-
K. Inoue, M. Yamashiro, and M. Iji Recyclable shape-memory polymer: poly(lactic acid) crosslinked by a thermoreversible Diels-Alder reaction J. Appl. Polym. Sci. 112 2009 876 885 10.1002/app.29469
-
(2009)
J. Appl. Polym. Sci.
, vol.112
, pp. 876-885
-
-
Inoue, K.1
Yamashiro, M.2
Iji, M.3
-
69
-
-
84856005307
-
Multifunctional poly(caprolactone)-forming networks by Diels-Alder cycloaddition: Effect of the adduct on the shape-memory properties
-
T. Defize, R. Riva, C. Jérôme, and M. Alexandre Multifunctional poly(caprolactone)-forming networks by Diels-Alder cycloaddition: effect of the adduct on the shape-memory properties Macromol. Chem. Phys. 213 2011 187 197 10.1002/macp.201100408
-
(2011)
Macromol. Chem. Phys.
, vol.213
, pp. 187-197
-
-
Defize, T.1
Riva, R.2
Jérôme, C.3
Alexandre, M.4
-
70
-
-
80051705229
-
Thermoreversibly crosslinked poly(ε-caprolactone) as recyclable shape-memory polymer network
-
T. Defize, R. Riva, J.-M. Raquez, P. Dubois, C. Jérôme, and M. Alexandre Thermoreversibly crosslinked poly(ε-caprolactone) as recyclable shape-memory polymer network Macromol. Rapid Commun. 32 2011 1264 1269 10.1002/marc.201100250
-
(2011)
Macromol. Rapid Commun.
, vol.32
, pp. 1264-1269
-
-
Defize, T.1
Riva, R.2
Raquez, J.-M.3
Dubois, P.4
Jérôme, C.5
Alexandre, M.6
-
71
-
-
84880080323
-
Reconfigurable biodegradable shape-memory elastomers via Diels-Alder coupling
-
C. Ninh, and C.J. Bettinger Reconfigurable biodegradable shape-memory elastomers via Diels-Alder coupling Biomacromolecules 14 2013 2162 2170 10.1021/bm4002602
-
(2013)
Biomacromolecules
, vol.14
, pp. 2162-2170
-
-
Ninh, C.1
Bettinger, C.J.2
-
72
-
-
0037204998
-
Biodegradable, elastic shape-memory polymers for potential biomedical applications
-
A. Lendlein, and R. Langer Biodegradable, elastic shape-memory polymers for potential biomedical applications Science 296 2002 1673 1676 10.1126/science.1066102
-
(2002)
Science
, vol.296
, pp. 1673-1676
-
-
Lendlein, A.1
Langer, R.2
-
73
-
-
77951832882
-
Shape-memory polymers as a technology platform for biomedical applications
-
A. Lendlein, M. Behl, B. Hiebl, and C. Wischke Shape-memory polymers as a technology platform for biomedical applications Expert Rev. Med. Devices 7 2010 357 379 10.1586/erd.10.8
-
(2010)
Expert Rev. Med. Devices
, vol.7
, pp. 357-379
-
-
Lendlein, A.1
Behl, M.2
Hiebl, B.3
Wischke, C.4
-
74
-
-
84856875815
-
Synthesis and functionalization of thiol-reactive biodegradable polymers
-
S. Onbulak, S. Tempelaar, R.J. Pounder, O. Gok, R. Sanyal, A.P. Dove, and et al. Synthesis and functionalization of thiol-reactive biodegradable polymers Macromolecules 45 2012 1715 1722 10.1021/ma2019528
-
(2012)
Macromolecules
, vol.45
, pp. 1715-1722
-
-
Onbulak, S.1
Tempelaar, S.2
Pounder, R.J.3
Gok, O.4
Sanyal, R.5
Dove, A.P.6
-
75
-
-
11444268404
-
Synthesis of organic-inorganic polymer hybrids controlled by Diels-Alder reaction
-
K. Adachi, A.K. Achimuthu, and Y. Chujo Synthesis of organic-inorganic polymer hybrids controlled by Diels-Alder reaction Macromolecules 37 2004 9793 9797 10.1021/ma0400618
-
(2004)
Macromolecules
, vol.37
, pp. 9793-9797
-
-
Adachi, K.1
Achimuthu, A.K.2
Chujo, Y.3
-
76
-
-
77957877707
-
Biodegradable polymer matrix nanocomposites for tissue engineering: A review
-
I. Armentano, M. Dottori, E. Fortunati, S. Mattioli, and J.M. Kenny Biodegradable polymer matrix nanocomposites for tissue engineering: a review Polym. Degrad. Stab. 95 2010 2126 2146 10.1016/j.polymdegradstab.2010.06.007
-
(2010)
Polym. Degrad. Stab.
, vol.95
, pp. 2126-2146
-
-
Armentano, I.1
Dottori, M.2
Fortunati, E.3
Mattioli, S.4
Kenny, J.M.5
-
77
-
-
33644999340
-
Preparation of block copolymers via Diels Alder reaction of maleimide- and anthracene-end functionalized polymers
-
H. Durmaz, B. Colakoglu, U. Tunca, and G. Hizal Preparation of block copolymers via Diels Alder reaction of maleimide- and anthracene-end functionalized polymers J. Polym. Sci. A: Polym. Chem. 44 2006 1667 1675 10.1002/pola.21275
-
(2006)
J. Polym. Sci. A: Polym. Chem.
, vol.44
, pp. 1667-1675
-
-
Durmaz, H.1
Colakoglu, B.2
Tunca, U.3
Hizal, G.4
-
78
-
-
33748323509
-
Anthracene-maleimide-based Diels-Alder "click chemistry" as a novel route to graft copolymers
-
B. Gacal, H. Durmaz, M.A. Tasdelen, G. Hizal, U. Tunca, Y. Yagci, and et al. Anthracene-maleimide-based Diels-Alder "click chemistry" as a novel route to graft copolymers Macromolecules 39 2006 5330 5336 10.1021/ma060690c
-
(2006)
Macromolecules
, vol.39
, pp. 5330-5336
-
-
Gacal, B.1
Durmaz, H.2
Tasdelen, M.A.3
Hizal, G.4
Tunca, U.5
Yagci, Y.6
-
79
-
-
58149196356
-
Multiarm star block copolymers via Diels-Alder click reaction
-
A. Dag, H. Durmaz, U. Tunca, and G. Hizal Multiarm star block copolymers via Diels-Alder click reaction J. Polym. Sci. A: Polym. Chem. 47 2009 178 187 10.1002/pola.23140
-
(2009)
J. Polym. Sci. A: Polym. Chem.
, vol.47
, pp. 178-187
-
-
Dag, A.1
Durmaz, H.2
Tunca, U.3
Hizal, G.4
-
80
-
-
84894042002
-
Synthesis and characterization of biodegradable amphiphilic star and Y-shaped block copolymers as potential carriers for vinorelbine
-
F. Bahadori, A. Dag, H. Durmaz, N. Cakir, H. Onyuksel, U. Tunca, and et al. Synthesis and characterization of biodegradable amphiphilic star and Y-shaped block copolymers as potential carriers for vinorelbine Polymers 6 2014 214 242 10.3390/polym6010214
-
(2014)
Polymers
, vol.6
, pp. 214-242
-
-
Bahadori, F.1
Dag, A.2
Durmaz, H.3
Cakir, N.4
Onyuksel, H.5
Tunca, U.6
-
81
-
-
0032683045
-
Cross-linking and modification of poly(ethylene terephthalate-co-2,6-anthracenedicarboxylate) by Diels-Alder reactions with maleimides
-
J.R. Jones, C.L. Liotta, D.M. Collard, and D.A. Schiraldi Cross-linking and modification of poly(ethylene terephthalate-co-2,6-anthracenedicarboxylate) by Diels-Alder reactions with maleimides Macromolecules 32 1999 5786 5792 10.1021/ma990638z
-
(1999)
Macromolecules
, vol.32
, pp. 5786-5792
-
-
Jones, J.R.1
Liotta, C.L.2
Collard, D.M.3
Schiraldi, D.A.4
-
82
-
-
33846974308
-
One-pot synthesis of ABC type triblock copolymers via in situ click [3 + 2] and Diels-Alder [4 + 2] reactions
-
H. Durmaz, A. Dag, O. Altintas, T. Erdogan, G. Hizal, and U. Tunca One-pot synthesis of ABC type triblock copolymers via in situ click [3 + 2] and Diels-Alder [4 + 2] reactions Macromolecules 40 2007 191 198 10.1021/ma061819l
-
(2007)
Macromolecules
, vol.40
, pp. 191-198
-
-
Durmaz, H.1
Dag, A.2
Altintas, O.3
Erdogan, T.4
Hizal, G.5
Tunca, U.6
-
83
-
-
70349782273
-
Ultrafast click conjugation of macromolecular building blocks at ambient temperature
-
A.J. Inglis, S. Sinnwell, M.H. Stenzel, and C. Barner-Kowollik Ultrafast click conjugation of macromolecular building blocks at ambient temperature Angew. Chem. Int. Ed. 48 2009 2411 2414 10.1002/anie.200805993
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 2411-2414
-
-
Inglis, A.J.1
Sinnwell, S.2
Stenzel, M.H.3
Barner-Kowollik, C.4
-
84
-
-
77950560790
-
Synthesis of comb polymers via grafting-onto macromolecules bearing pendant diene groups via the hetero-Diels-Alder-RAFT click concept
-
A. Bousquet, C. Barner-Kowollik, and M.H. Stenzel Synthesis of comb polymers via grafting-onto macromolecules bearing pendant diene groups via the hetero-Diels-Alder-RAFT click concept J. Polym. Sci. A: Polym. Chem. 48 2010 1773 1781 10.1002/pola.23943
-
(2010)
J. Polym. Sci. A: Polym. Chem.
, vol.48
, pp. 1773-1781
-
-
Bousquet, A.1
Barner-Kowollik, C.2
Stenzel, M.H.3
-
85
-
-
37049082120
-
The "inverse electron-demand" Diels-Alder reaction in polymer synthesis. Part 1. A convenient synthetic route to diethyl aromatic compounds
-
B.J.L. Royles, and D.M. Smith The "inverse electron-demand" Diels-Alder reaction in polymer synthesis. Part 1. A convenient synthetic route to diethyl aromatic compounds J. Chem. Soc. Perkin Trans. 1 1994 355 358 10.1039/p19940000355
-
(1994)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 355-358
-
-
Royles, B.J.L.1
Smith, D.M.2
-
86
-
-
37049087811
-
The "inverse electron-demand" Diels-Alder reaction in polymer synthesis. Part 2. Some bis(1,2,4-triazines) as potential bis-diene monomers
-
M.J. Bruce, G.A. McLean, B.J.L. Royles, D.M. Smith, and P.N. Standring The "inverse electron-demand" Diels-Alder reaction in polymer synthesis. Part 2. Some bis(1,2,4-triazines) as potential bis-diene monomers J. Chem. Soc. Perkin Trans. 1 1995 1789 10.1039/p19950001789
-
(1995)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 1789
-
-
Bruce, M.J.1
McLean, G.A.2
Royles, B.J.L.3
Smith, D.M.4
Standring, P.N.5
-
87
-
-
80052327714
-
Additive-free clicking for polymer functionalization and coupling by tetrazine-norbornene chemistry
-
C.F. Hansell, P. Espeel, M.M. Stamenović, I.A. Barker, A.P. Dove, F.E. Du Prez, and et al. Additive-free clicking for polymer functionalization and coupling by tetrazine-norbornene chemistry J. Am. Chem. Soc. 133 2011 13828 13831 10.1021/ja203957h
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13828-13831
-
-
Hansell, C.F.1
Espeel, P.2
Stamenović, M.M.3
Barker, I.A.4
Dove, A.P.5
Du Prez, F.E.6
-
88
-
-
84862227297
-
Tetrazine-norbornene click reactions to functionalize degradable polymers derived from lactide
-
I.A. Barker, D.J. Hall, C.F. Hansell, F.E. Du Prez, R.K. O'Reilly, and A.P. Dove Tetrazine-norbornene click reactions to functionalize degradable polymers derived from lactide Macromol. Rapid Commun. 32 2011 1362 1366 10.1002/marc.201100324
-
(2011)
Macromol. Rapid Commun.
, vol.32
, pp. 1362-1366
-
-
Barker, I.A.1
Hall, D.J.2
Hansell, C.F.3
Du Prez, F.E.4
O'Reilly, R.K.5
Dove, A.P.6
-
89
-
-
33746880657
-
Synthesis of star polymers by a combination of ATRP and the "click" coupling method
-
H. Gao, and K. Matyjaszewski Synthesis of star polymers by a combination of ATRP and the "click" coupling method Macromolecules 39 2006 4960 4965 10.1021/ma060926c
-
(2006)
Macromolecules
, vol.39
, pp. 4960-4965
-
-
Gao, H.1
Matyjaszewski, K.2
-
90
-
-
35248895384
-
New poly(acrylic acid) containing segmented copolymer structures by combination of "click" chemistry and atom transfer radical polymerization
-
W. Van Camp, V. Germonpré, L. Mespouille, P. Dubois, E.J. Goethals, and F.E. Du Prez New poly(acrylic acid) containing segmented copolymer structures by combination of "click" chemistry and atom transfer radical polymerization React. Funct. Polym. 67 2007 1168 1180 10.1016/j.reactfunctpolym.2007.07.004
-
(2007)
React. Funct. Polym.
, vol.67
, pp. 1168-1180
-
-
Van Camp, W.1
Germonpré, V.2
Mespouille, L.3
Dubois, P.4
Goethals, E.J.5
Du Prez, F.E.6
-
91
-
-
54849438531
-
Development of thermal and photochemical strategies for thiol-ene click polymer functionalization
-
L.M. Campos, K.L. Killops, R. Sakai, J.M.J. Paulusse, D. Damiron, E. Drockenmuller, and et al. Development of thermal and photochemical strategies for thiol-ene click polymer functionalization Macromolecules 41 2008 7063 7070 10.1021/ma801630n
-
(2008)
Macromolecules
, vol.41
, pp. 7063-7070
-
-
Campos, L.M.1
Killops, K.L.2
Sakai, R.3
Paulusse, J.M.J.4
Damiron, D.5
Drockenmuller, E.6
-
92
-
-
58349108839
-
Convergent synthesis of 3-arm star polymers from RAFT-prepared poly(N, N-diethylacrylamide) via a thiol-ene click reaction
-
J.W. Chan, B. Yu, C.E. Hoyle, and A.B. Lowe Convergent synthesis of 3-arm star polymers from RAFT-prepared poly(N, N-diethylacrylamide) via a thiol-ene click reaction Chem. Commun. 2008 4959 4961 10.1039/B813438C
-
(2008)
Chem. Commun.
, pp. 4959-4961
-
-
Chan, J.W.1
Yu, B.2
Hoyle, C.E.3
Lowe, A.B.4
-
93
-
-
0344466792
-
Designing dendrimers for drug delivery
-
M. Liu, and J.M.J. Fréchet Designing dendrimers for drug delivery Pharm. Sci. Technol. Today 2 1999 393 401 10.1016/S1461-5347(99)00203-5
-
(1999)
Pharm. Sci. Technol. Today
, vol.2
, pp. 393-401
-
-
Liu, M.1
Fréchet, J.M.J.2
-
94
-
-
12844258906
-
Dendrimers and dendritic polymers in drug delivery
-
E.R. Gillies, and J.M.J. Fréchet Dendrimers and dendritic polymers in drug delivery Drug Discov. Today 10 2005 35 43 10.1016/S1359-6446(04)03276-3
-
(2005)
Drug Discov. Today
, vol.10
, pp. 35-43
-
-
Gillies, E.R.1
Fréchet, J.M.J.2
-
96
-
-
33847759151
-
Dendrimers based on thermally reversible furan-maleimide Diels-Alder adducts
-
M.L. Szalai, D.V. McGrath, D.R. Wheeler, T. Zifer, and J.R. McElhanon Dendrimers based on thermally reversible furan-maleimide Diels-Alder adducts Macromolecules 40 2007 818 823 10.1021/ma062093w
-
(2007)
Macromolecules
, vol.40
, pp. 818-823
-
-
Szalai, M.L.1
McGrath, D.V.2
Wheeler, D.R.3
Zifer, T.4
McElhanon, J.R.5
-
97
-
-
0000598756
-
Thermally responsive dendrons and dendrimers based on reversible furan-maleimide Diels-Alder adducts
-
J.R. McElhanon, and D.R. Wheeler Thermally responsive dendrons and dendrimers based on reversible furan-maleimide Diels-Alder adducts Org. Lett. 3 2001 2681 2683 10.1021/ol0101281
-
(2001)
Org. Lett.
, vol.3
, pp. 2681-2683
-
-
McElhanon, J.R.1
Wheeler, D.R.2
-
98
-
-
77949405751
-
I-catalysed alkyne-azide cycloaddition and furan-maleimide Diels-Alder "click" chemistry approach to thermoresponsive dendrimers
-
I-catalysed alkyne-azide cycloaddition and furan-maleimide Diels-Alder "click" chemistry approach to thermoresponsive dendrimers Chem. Commun. 46 2010 1875 10.1039/b924888a
-
(2010)
Chem. Commun.
, vol.46
, pp. 1875
-
-
Vieyres, A.1
Lam, T.2
Gillet, R.3
Franc, G.4
Castonguay, A.5
Kakkar, A.6
-
99
-
-
76149146050
-
Thermally reversible dendronized step-polymers based on sequential Huisgen 1,3-dipolar cycloaddition and Diels-Alder "click" reactions
-
N.W. Polaske, D.V. McGrath, and J.R. McElhanon Thermally reversible dendronized step-polymers based on sequential Huisgen 1,3-dipolar cycloaddition and Diels-Alder "click" reactions Macromolecules 43 2010 1270 1276 10.1021/ma902180r
-
(2010)
Macromolecules
, vol.43
, pp. 1270-1276
-
-
Polaske, N.W.1
McGrath, D.V.2
McElhanon, J.R.3
-
100
-
-
80155174818
-
Thermosensitive dendrimer formulation for drug delivery at physiologically relevant temperatures
-
A. Castonguay, E. Wilson, N. Al-Hajaj, L. Petitjean, J. Paoletti, D. Maysinger, and et al. Thermosensitive dendrimer formulation for drug delivery at physiologically relevant temperatures Chem. Commun. 47 2011 12146 12148 10.1039/c1cc15354d
-
(2011)
Chem. Commun.
, vol.47
, pp. 12146-12148
-
-
Castonguay, A.1
Wilson, E.2
Al-Hajaj, N.3
Petitjean, L.4
Paoletti, J.5
Maysinger, D.6
-
101
-
-
48849103608
-
Segment block dendrimers via Diels-Alder cycloaddition
-
M.M. Kose, G. Yesilbag, and A. Sanyal Segment block dendrimers via Diels-Alder cycloaddition Org. Lett. 10 2008 2353 2356 10.1021/ol800553t
-
(2008)
Org. Lett.
, vol.10
, pp. 2353-2356
-
-
Kose, M.M.1
Yesilbag, G.2
Sanyal, A.3
-
102
-
-
0037415560
-
Diels-Alder reaction of anthracene and N-ethylmaleimide on the carbosilane dendrimer
-
C. Kim, H. Kim, and K. Park Diels-Alder reaction of anthracene and N-ethylmaleimide on the carbosilane dendrimer J. Organomet. Chem. 667 2003 96 102 10.1016/S0022-328X(02)02148-4
-
(2003)
J. Organomet. Chem.
, vol.667
, pp. 96-102
-
-
Kim, C.1
Kim, H.2
Park, K.3
-
103
-
-
26444474799
-
Preparation and Diels-Alder reaction of carbosilane dendrimer with conjugated diene
-
C. Kim, H. Kim, and K. Park Preparation and Diels-Alder reaction of carbosilane dendrimer with conjugated diene J. Organomet. Chem. 690 2005 4794 4800 10.1016/j.jorganchem.2005.07.079
-
(2005)
J. Organomet. Chem.
, vol.690
, pp. 4794-4800
-
-
Kim, C.1
Kim, H.2
Park, K.3
-
104
-
-
21844449921
-
Spherical polyphenylene dendrimers via Diels-Alder reactions: The first example of an A4B building block in dendrimer chemistry
-
F. Morgenroth Spherical polyphenylene dendrimers via Diels-Alder reactions: the first example of an A4B building block in dendrimer chemistry Chem. Commun. 1998 1139 1140 10.1039/a801395k
-
(1998)
Chem. Commun.
, pp. 1139-1140
-
-
Morgenroth, F.1
-
105
-
-
72949094190
-
Dendronized polymers via Diels-Alder "click" reaction
-
M. Tonga, N. Cengiz, M.M. Kose, T. Dede, and A. Sanyal Dendronized polymers via Diels-Alder "click" reaction J. Polym. Sci. A: Polym. Chem. 48 2010 410 416 10.1002/pola.23799
-
(2010)
J. Polym. Sci. A: Polym. Chem.
, vol.48
, pp. 410-416
-
-
Tonga, M.1
Cengiz, N.2
Kose, M.M.3
Dede, T.4
Sanyal, A.5
-
106
-
-
84879418205
-
Dendron-polymer conjugates via the Diels-alder "click" reaction of novel anthracene-based dendrons
-
O. Gok, S. Yigit, M. Merve Kose, R. Sanyal, and A. Sanyal Dendron-polymer conjugates via the Diels-alder "click" reaction of novel anthracene-based dendrons J. Polym. Sci. A: Polym. Chem. 51 2013 3191 3201 10.1002/pola.26708
-
(2013)
J. Polym. Sci. A: Polym. Chem.
, vol.51
, pp. 3191-3201
-
-
Gok, O.1
Yigit, S.2
Merve Kose, M.3
Sanyal, R.4
Sanyal, A.5
-
107
-
-
77952973051
-
Maleimide-based thiol reactive multiarm star polymers via Diels-Alder/retro Diels-Alder strategy
-
O. Gok, H. Durmaz, E.S. Ozdes, G. Hizal, U. Tunca, and A. Sanyal Maleimide-based thiol reactive multiarm star polymers via Diels-Alder/retro Diels-Alder strategy J. Polym. Sci. A: Polym. Chem. 48 2010 2546 2556 10.1002/pola.24030
-
(2010)
J. Polym. Sci. A: Polym. Chem.
, vol.48
, pp. 2546-2556
-
-
Gok, O.1
Durmaz, H.2
Ozdes, E.S.3
Hizal, G.4
Tunca, U.5
Sanyal, A.6
-
108
-
-
0042562089
-
Biomimetic materials for tissue engineering
-
H. Shin, S. Jo, and A.G. Mikos Biomimetic materials for tissue engineering Biomaterials 24 2003 4353 4364 10.1016/S0142-9612(03)00339-9
-
(2003)
Biomaterials
, vol.24
, pp. 4353-4364
-
-
Shin, H.1
Jo, S.2
Mikos, A.G.3
-
109
-
-
0042061223
-
Hydrogels for tissue engineering: Scaffold design variables and applications
-
J.L. Drury, and D.J. Mooney Hydrogels for tissue engineering: scaffold design variables and applications Biomaterials 24 2003 4337 4351 10.1016/S0142-9612(03)00340-5
-
(2003)
Biomaterials
, vol.24
, pp. 4337-4351
-
-
Drury, J.L.1
Mooney, D.J.2
-
110
-
-
0021271957
-
Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule
-
M.D. Pierschbacher, and E. Ruoslahti Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule Nature 309 1984 30 33 10.1038/309030a0
-
(1984)
Nature
, vol.309
, pp. 30-33
-
-
Pierschbacher, M.D.1
Ruoslahti, E.2
-
111
-
-
0041559949
-
RGD modified polymers: Biomaterials for stimulated cell adhesion and beyond
-
U. Hersel, C. Dahmen, and H. Kessler RGD modified polymers: biomaterials for stimulated cell adhesion and beyond Biomaterials 24 2003 4385 4415 10.1016/S0142-9612(03)00343-0
-
(2003)
Biomaterials
, vol.24
, pp. 4385-4415
-
-
Hersel, U.1
Dahmen, C.2
Kessler, H.3
-
112
-
-
33747157139
-
Diels-Alder ligation of peptides and proteins
-
A.D. de Araújo, J.M. Palomo, J. Cramer, O. Seitz, K. Alexandrov, and H. Waldmann Diels-Alder ligation of peptides and proteins Chem. Eur. J. 12 2006 6095 6109 10.1002/chem.200600148
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 6095-6109
-
-
De Araújo, A.D.1
Palomo, J.M.2
Cramer, J.3
Seitz, O.4
Alexandrov, K.5
Waldmann, H.6
-
113
-
-
40849114388
-
Chemoselective immobilization of biomolecules through aqueous Diels-Alder and PEG chemistry
-
X.-L. Sun, L. Yang, and E.L. Chaikof Chemoselective immobilization of biomolecules through aqueous Diels-Alder and PEG chemistry Tetrahedron Lett. 49 2008 2510 2513 10.1016/j.tetlet.2008.02.111
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 2510-2513
-
-
Sun, X.-L.1
Yang, L.2
Chaikof, E.L.3
-
114
-
-
31544446908
-
Carbohydrate and protein immobilization onto solid surfaces by sequential Diels-Alder and azide-alkyne cycloadditions
-
X.-L. Sun, C.L. Stabler, C.S. Cazalis, and E.L. Chaikof Carbohydrate and protein immobilization onto solid surfaces by sequential Diels-Alder and azide-alkyne cycloadditions Bioconjugate Chem. 17 2006 52 57 10.1021/bc0502311
-
(2006)
Bioconjugate Chem.
, vol.17
, pp. 52-57
-
-
Sun, X.-L.1
Stabler, C.L.2
Cazalis, C.S.3
Chaikof, E.L.4
-
115
-
-
0344667476
-
Dynamic interfaces between cells and surfaces: Electroactive substrates that sequentially release and attach cells
-
W.-S. Yeo, M.N. Yousaf, and M. Mrksich Dynamic interfaces between cells and surfaces: electroactive substrates that sequentially release and attach cells J. Am. Chem. Soc. 125 2003 14994 14995 10.1021/ja038265b
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 14994-14995
-
-
Yeo, W.-S.1
Yousaf, M.N.2
Mrksich, M.3
-
116
-
-
84871028409
-
3D Photofixation lithography in Diels-Alder networks
-
B.J. Adzima, C.J. Kloxin, C.A. DeForest, K.S. Anseth, and C.N. Bowman 3D Photofixation lithography in Diels-Alder networks Macromol. Rapid Commun. 33 2012 2092 2096 10.1002/marc.201200599
-
(2012)
Macromol. Rapid Commun.
, vol.33
, pp. 2092-2096
-
-
Adzima, B.J.1
Kloxin, C.J.2
DeForest, C.A.3
Anseth, K.S.4
Bowman, C.N.5
-
117
-
-
84855700093
-
Photoreactive polymer brushes for high-density patterned surface derivatization using a Diels-Alder photoclick reaction
-
S. Arumugam, S.V. Orski, J. Locklin, and V.V. Popik Photoreactive polymer brushes for high-density patterned surface derivatization using a Diels-Alder photoclick reaction J. Am. Chem. Soc. 134 2012 179 182 10.1021/ja210350d
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 179-182
-
-
Arumugam, S.1
Orski, S.V.2
Locklin, J.3
Popik, V.V.4
-
118
-
-
26644452794
-
Studies on the attachment of DNA to silica-coated nanoparticles through a Diels-Alder reaction
-
M. Proupin-Perez, R. Cosstick, L.M. Liz-Marzan, V. Salgueiriño-Maceira, and M. Brust Studies on the attachment of DNA to silica-coated nanoparticles through a Diels-Alder reaction Nucleos. Nucleot. Nucleic Acids 24 2005 1075 1079 10.1081/NCN-200059170
-
(2005)
Nucleos. Nucleot. Nucleic Acids
, vol.24
, pp. 1075-1079
-
-
Proupin-Perez, M.1
Cosstick, R.2
Liz-Marzan, L.M.3
Salgueiriño-Maceira, V.4
Brust, M.5
-
119
-
-
50249128702
-
Furan-functionalized co-polymers for targeted drug delivery: Characterization, self-assembly and drug encapsulation
-
M. Shi, and M.S. Shoichet Furan-functionalized co-polymers for targeted drug delivery: characterization, self-assembly and drug encapsulation J. Biomater. Sci. Polym. Ed. 19 2008 1143 1157 10.1163/156856208785540127
-
(2008)
J. Biomater. Sci. Polym. Ed.
, vol.19
, pp. 1143-1157
-
-
Shi, M.1
Shoichet, M.S.2
-
120
-
-
34548080032
-
Immuno-polymeric nanoparticles by Diels-Alder chemistry
-
M. Shi, J.H. Wosnick, K. Ho, A. Keating, and M.S. Shoichet Immuno-polymeric nanoparticles by Diels-Alder chemistry Angew. Chem. 119 2007 6238 6243 10.1002/ange.200701032
-
(2007)
Angew. Chem.
, vol.119
, pp. 6238-6243
-
-
Shi, M.1
Wosnick, J.H.2
Ho, K.3
Keating, A.4
Shoichet, M.S.5
-
121
-
-
67649238437
-
Doxorubicin-conjugated immuno-nanoparticles for intracellular anticancer drug delivery
-
M. Shi, K. Ho, A. Keating, and M.S. Shoichet Doxorubicin-conjugated immuno-nanoparticles for intracellular anticancer drug delivery Adv. Funct. Mater. 19 2009 1689 1696 10.1002/adfm.200801271
-
(2009)
Adv. Funct. Mater.
, vol.19
, pp. 1689-1696
-
-
Shi, M.1
Ho, K.2
Keating, A.3
Shoichet, M.S.4
-
122
-
-
84872543247
-
Double click: Dual functionalized polymeric micelles with antibodies and peptides
-
D.P.Y. Chan, S.C. Owen, and M.S. Shoichet Double click: dual functionalized polymeric micelles with antibodies and peptides Bioconjugate Chem. 24 2013 105 113 10.1021/bc300511a
-
(2013)
Bioconjugate Chem.
, vol.24
, pp. 105-113
-
-
Chan, D.P.Y.1
Owen, S.C.2
Shoichet, M.S.3
-
123
-
-
84881670224
-
Click conjugated polymeric immuno-nanoparticles for targeted siRNA and antisense oligonucleotide delivery
-
D.P.Y. Chan, G.F. Deleavey, S.C. Owen, M.J. Damha, and M.S. Shoichet Click conjugated polymeric immuno-nanoparticles for targeted siRNA and antisense oligonucleotide delivery Biomaterials 34 2013 8408 8415 10.1016/j.biomaterials.2013.07.019
-
(2013)
Biomaterials
, vol.34
, pp. 8408-8415
-
-
Chan, D.P.Y.1
Deleavey, G.F.2
Owen, S.C.3
Damha, M.J.4
Shoichet, M.S.5
-
124
-
-
77955586451
-
Heterotelechelic polymers for capture and release of protein-polymer conjugates
-
K.L. Heredia, L. Tao, G.N. Grover, and H.D. Maynard Heterotelechelic polymers for capture and release of protein-polymer conjugates Polym. Chem. 1 2010 168 170 10.1039/B9PY00369J
-
(2010)
Polym. Chem.
, vol.1
, pp. 168-170
-
-
Heredia, K.L.1
Tao, L.2
Grover, G.N.3
Maynard, H.D.4
-
125
-
-
14844329852
-
Design and synthesis of N-maleimido-functionalized hydrophilic polymers via copper-mediated living radical polymerization: A suitable alternative to PEGylation chemistry
-
G. Mantovani, F. Lecolley, L. Tao, D.M. Haddleton, J. Clerx, J.J.L.M. Cornelissen, and et al. Design and synthesis of N-maleimido-functionalized hydrophilic polymers via copper-mediated living radical polymerization: a suitable alternative to PEGylation chemistry J. Am. Chem. Soc. 127 2005 2966 2973 10.1021/ja0430999
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2966-2973
-
-
Mantovani, G.1
Lecolley, F.2
Tao, L.3
Haddleton, D.M.4
Clerx, J.5
Cornelissen, J.J.L.M.6
-
126
-
-
1642314171
-
Interior surface modification of bacteriophage MS2
-
J.M. Hooker, E.W. Kovacs, and M.B. Francis Interior surface modification of bacteriophage MS2 J. Am. Chem. Soc. 126 2004 3718 3719 10.1021/ja031790q
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 3718-3719
-
-
Hooker, J.M.1
Kovacs, E.W.2
Francis, M.B.3
-
127
-
-
0037136489
-
A method for bioconjugation of carbohydrates using Diels-Alder cycloaddition
-
V. Pozsgay, N.E. Vieira, and A. Yergey A method for bioconjugation of carbohydrates using Diels-Alder cycloaddition Org. Lett. 4 2002 3191 3194 10.1021/ol026179v
-
(2002)
Org. Lett.
, vol.4
, pp. 3191-3194
-
-
Pozsgay, V.1
Vieira, N.E.2
Yergey, A.3
-
128
-
-
33644853492
-
Diels-Alder cycloadditions in water for the straightforward preparation of peptide-oligonucleotide conjugates
-
V. Marchán, S. Ortega, D. Pulido, E. Pedroso, and A. Grandas Diels-Alder cycloadditions in water for the straightforward preparation of peptide-oligonucleotide conjugates Nucleic Acids Res. 34 2006 e24 10.1093/nar/gnj020
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. e24
-
-
Marchán, V.1
Ortega, S.2
Pulido, D.3
Pedroso, E.4
Grandas, A.5
-
129
-
-
53849105464
-
Tetrazine ligation: Fast bioconjugation based on inverse-electron-demand Diels-Alder reactivity
-
M.L. Blackman, M. Royzen, and J.M. Fox Tetrazine ligation: fast bioconjugation based on inverse-electron-demand Diels-Alder reactivity J. Am. Chem. Soc. 130 2008 13518 13519 10.1021/ja8053805
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 13518-13519
-
-
Blackman, M.L.1
Royzen, M.2
Fox, J.M.3
-
130
-
-
76149118438
-
The Diels-Alder-reaction with inverse-electron-demand, a very efficient versatile click-reaction concept for proper ligation of variable molecular partners
-
M. Wiessler, W. Waldeck, C. Kliem, R. Pipkorn, and K. Braun The Diels-Alder-reaction with inverse-electron-demand, a very efficient versatile click-reaction concept for proper ligation of variable molecular partners Int. J. Med. Sci. 7 2009 19 28 10.7150/ijms.7.19
-
(2009)
Int. J. Med. Sci.
, vol.7
, pp. 19-28
-
-
Wiessler, M.1
Waldeck, W.2
Kliem, C.3
Pipkorn, R.4
Braun, K.5
-
131
-
-
84862907995
-
Diels-Alder cycloaddition for fluorophore targeting to specific proteins inside living cells
-
D.S. Liu, A. Tangpeerachaikul, R. Selvaraj, M.T. Taylor, J.M. Fox, and A.Y. Ting Diels-Alder cycloaddition for fluorophore targeting to specific proteins inside living cells J. Am. Chem. Soc. 134 2012 792 795 10.1021/ja209325n
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 792-795
-
-
Liu, D.S.1
Tangpeerachaikul, A.2
Selvaraj, R.3
Taylor, M.T.4
Fox, J.M.5
Ting, A.Y.6
-
132
-
-
84891690168
-
Diels-Alder reaction for tumor pretargeting: In vivo chemistry can boost tumor radiation dose compared with directly labeled antibody
-
R. Rossin, T. Läppchen, S.M. van den Bosch, R. Laforest, and M.S. Robillard Diels-Alder reaction for tumor pretargeting: in vivo chemistry can boost tumor radiation dose compared with directly labeled antibody J. Nucl. Med. 54 2013 1989 1995 10.2967/jnumed.113.123745
-
(2013)
J. Nucl. Med.
, vol.54
, pp. 1989-1995
-
-
Rossin, R.1
Läppchen, T.2
Van Den Bosch, S.M.3
Laforest, R.4
Robillard, M.S.5
-
133
-
-
84881407469
-
A pretargeted PET imaging strategy based on bioorthogonal Diels-Alder click chemistry
-
B.M. Zeglis, K.K. Sevak, T. Reiner, P. Mohindra, S.D. Carlin, P. Zanzonico, and et al. A pretargeted PET imaging strategy based on bioorthogonal Diels-Alder click chemistry J. Nucl. Med. 54 2013 1389 1396 10.2967/jnumed.112.115840
-
(2013)
J. Nucl. Med.
, vol.54
, pp. 1389-1396
-
-
Zeglis, B.M.1
Sevak, K.K.2
Reiner, T.3
Mohindra, P.4
Carlin, S.D.5
Zanzonico, P.6
-
134
-
-
63449127358
-
Inverse-electron-demand Diels-Alder reaction as a highly efficient chemoselective ligation procedure: Synthesis and function of a BioShuttle for temozolomide transport into prostate cancer cells
-
R. Pipkorn, W. Waldeck, B. Didinger, M. Koch, G. Mueller, M. Wiessler, and et al. Inverse-electron-demand Diels-Alder reaction as a highly efficient chemoselective ligation procedure: synthesis and function of a BioShuttle for temozolomide transport into prostate cancer cells J. Pept. Sci. 15 2009 235 241 10.1002/psc.1108
-
(2009)
J. Pept. Sci.
, vol.15
, pp. 235-241
-
-
Pipkorn, R.1
Waldeck, W.2
Didinger, B.3
Koch, M.4
Mueller, G.5
Wiessler, M.6
-
135
-
-
74549156558
-
Treatment of glioblastoma multiforme cells with temozolomide-BioShuttle ligated by the inverse Diels-Alder ligation chemistry
-
K. Braun Treatment of glioblastoma multiforme cells with temozolomide-BioShuttle ligated by the inverse Diels-Alder ligation chemistry DDDT 2009 289 10.2147/DDDT.S3572
-
(2009)
DDDT
, pp. 289
-
-
Braun, K.1
-
136
-
-
84890704870
-
Click to release: Instantaneous doxorubicin elimination upon tetrazine ligation
-
R.M. Versteegen, R. Rossin, W. ten Hoeve, H.M. Janssen, and M.S. Robillard Click to release: instantaneous doxorubicin elimination upon tetrazine ligation Angew. Chem. Int. Ed. 52 2013 14112 14116 10.1002/anie.201305969
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 14112-14116
-
-
Versteegen, R.M.1
Rossin, R.2
Ten Hoeve, W.3
Janssen, H.M.4
Robillard, M.S.5
-
137
-
-
34548715186
-
Metal-free triazole formation as a tool for bioconjugation
-
S.S. van Berkel, A.T.J. Dirks, M.F. Debets, F.L. van Delft, J.J.L.M. Cornelissen, R.J.M. Nolte, and et al. Metal-free triazole formation as a tool for bioconjugation ChemBioChem 8 2007 1504 1508 10.1002/cbic.200700278
-
(2007)
ChemBioChem
, vol.8
, pp. 1504-1508
-
-
Van Berkel, S.S.1
Dirks, A.T.J.2
Debets, M.F.3
Van Delft, F.L.4
Cornelissen, J.J.L.M.5
Nolte, R.J.M.6
-
139
-
-
77956434412
-
Nanotechnology in drug delivery and tissue engineering: From discovery to applications
-
J. Shi, A.R. Votruba, O.C. Farokhzad, and R. Langer Nanotechnology in drug delivery and tissue engineering: from discovery to applications Nano Lett. 10 2010 3223 3230 10.1021/nl102184c
-
(2010)
Nano Lett.
, vol.10
, pp. 3223-3230
-
-
Shi, J.1
Votruba, A.R.2
Farokhzad, O.C.3
Langer, R.4
-
140
-
-
84867381407
-
Dynamic-covalent nanostructures prepared by Diels-Alder reactions of styrene-maleic anhydride-derived copolymers obtained by one-step cascade block copolymerization
-
A.P. Bapat, J.G. Ray, D.A. Savin, E.A. Hoff, D.L. Patton, and B.S. Sumerlin Dynamic-covalent nanostructures prepared by Diels-Alder reactions of styrene-maleic anhydride-derived copolymers obtained by one-step cascade block copolymerization Polym. Chem. 3 2012 3112 3120 10.1039/C2PY20351K
-
(2012)
Polym. Chem.
, vol.3
, pp. 3112-3120
-
-
Bapat, A.P.1
Ray, J.G.2
Savin, D.A.3
Hoff, E.A.4
Patton, D.L.5
Sumerlin, B.S.6
-
141
-
-
33846142171
-
Controlling dispersion and migration of particulate additives with block copolymers and Diels-Alder chemistry
-
P.J. Costanzo, J.D. Demaree, and F.L. Beyer Controlling dispersion and migration of particulate additives with block copolymers and Diels-Alder chemistry Langmuir 22 2006 10251 10257 10.1021/la0624541
-
(2006)
Langmuir
, vol.22
, pp. 10251-10257
-
-
Costanzo, P.J.1
Demaree, J.D.2
Beyer, F.L.3
-
142
-
-
34250707927
-
Thermally driven assembly of nanoparticles in polymer matrices
-
P.J. Costanzo, and F.L. Beyer Thermally driven assembly of nanoparticles in polymer matrices Macromolecules 40 2007 3996 4001 10.1021/ma070447t
-
(2007)
Macromolecules
, vol.40
, pp. 3996-4001
-
-
Costanzo, P.J.1
Beyer, F.L.2
-
143
-
-
79960492849
-
Direct fabrication of functional and biofunctional nanostructures through reactive imprinting
-
C. Subramani, N. Cengiz, K. Saha, T.N. Gevrek, X. Yu, Y. Jeong, and et al. Direct fabrication of functional and biofunctional nanostructures through reactive imprinting Adv. Mater. 23 2011 3165 3169 10.1002/adma.201101292
-
(2011)
Adv. Mater.
, vol.23
, pp. 3165-3169
-
-
Subramani, C.1
Cengiz, N.2
Saha, K.3
Gevrek, T.N.4
Yu, X.5
Jeong, Y.6
-
144
-
-
70349928775
-
An efficient method based on the photothermal effect for the release of molecules from metal nanoparticle surfaces
-
A.B.S. Bakhtiari, D. Hsiao, G. Jin, B.D. Gates, and N.R. Branda An efficient method based on the photothermal effect for the release of molecules from metal nanoparticle surfaces Angew. Chem. Int. Ed. 48 2009 4166 4169 10.1002/anie.200805303
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 4166-4169
-
-
Bakhtiari, A.B.S.1
Hsiao, D.2
Jin, G.3
Gates, B.D.4
Branda, N.R.5
-
145
-
-
82455188610
-
Controlled-release system mediated by a retro Diels-Alder reaction induced by the photothermal effect of gold nanorods
-
S. Yamashita, H. Fukushima, Y. Niidome, T. Mori, Y. Katayama, and T. Niidome Controlled-release system mediated by a retro Diels-Alder reaction induced by the photothermal effect of gold nanorods Langmuir 27 2011 14621 14626 10.1021/la2036746
-
(2011)
Langmuir
, vol.27
, pp. 14621-14626
-
-
Yamashita, S.1
Fukushima, H.2
Niidome, Y.3
Mori, T.4
Katayama, Y.5
Niidome, T.6
-
146
-
-
84861076436
-
Hydrogels for protein delivery
-
T. Vermonden, R. Censi, and W.E. Hennink Hydrogels for protein delivery Chem. Rev. 112 2012 2853 2888 10.1021/cr200157d
-
(2012)
Chem. Rev.
, vol.112
, pp. 2853-2888
-
-
Vermonden, T.1
Censi, R.2
Hennink, W.E.3
-
147
-
-
84884285139
-
Dextran-based self-healing hydrogels formed by reversible Diels-Alder reaction under physiological conditions
-
Z. Wei, J.H. Yang, X.J. Du, F. Xu, M. Zrinyi, Y. Osada, and et al. Dextran-based self-healing hydrogels formed by reversible Diels-Alder reaction under physiological conditions Macromol. Rapid Commun. 34 2013 1464 1470 10.1002/marc.201300494
-
(2013)
Macromol. Rapid Commun.
, vol.34
, pp. 1464-1470
-
-
Wei, Z.1
Yang, J.H.2
Du, X.J.3
Xu, F.4
Zrinyi, M.5
Osada, Y.6
-
148
-
-
77950864212
-
Characterisation of N-vinyl-2-pyrrolidone-based hydrogels prepared by a Diels-Alder click reaction in water
-
H.-L. Wei, Z. Yang, Y. Chen, H.-J. Chu, J. Zhu, and Z.-C. Li Characterisation of N-vinyl-2-pyrrolidone-based hydrogels prepared by a Diels-Alder click reaction in water Eur. Polym. J. 46 2010 1032 1039 10.1016/j.eurpolymj.2010.01.025
-
(2010)
Eur. Polym. J.
, vol.46
, pp. 1032-1039
-
-
Wei, H.-L.1
Yang, Z.2
Chen, Y.3
Chu, H.-J.4
Zhu, J.5
Li, Z.-C.6
-
149
-
-
77949875589
-
Facile preparation of poly(N-isopropylacrylamide)-based hydrogels via aqueous Diels-Alder click reaction
-
H.-L. Wei, Z. Yang, H.-J. Chu, J. Zhu, Z.-C. Li, and J.-S. Cui Facile preparation of poly(N-isopropylacrylamide)-based hydrogels via aqueous Diels-Alder click reaction Polymer 51 2010 1694 1702 10.1016/j.polymer.2010.02.008
-
(2010)
Polymer
, vol.51
, pp. 1694-1702
-
-
Wei, H.-L.1
Yang, Z.2
Chu, H.-J.3
Zhu, J.4
Li, Z.-C.5
Cui, J.-S.6
-
150
-
-
84855521593
-
Click synthesis of the thermo- and pH-sensitive hydrogels containing β-cyclodextrins
-
H.-L. Wei, K. Yao, H.-J. Chu, Z.-C. Li, J. Zhu, Y.-M. Shen, and et al. Click synthesis of the thermo- and pH-sensitive hydrogels containing β-cyclodextrins J. Mater. Sci. 47 2011 332 340 10.1007/s10853-011-5802-3
-
(2011)
J. Mater. Sci.
, vol.47
, pp. 332-340
-
-
Wei, H.-L.1
Yao, K.2
Chu, H.-J.3
Li, Z.-C.4
Zhu, J.5
Shen, Y.-M.6
-
151
-
-
84856021060
-
Properties of reversible Diels-Alder furan/maleimide polymer networks as function of crosslink density
-
C. Toncelli, D.C. De Reus, F. Picchioni, and A.A. Broekhuis Properties of reversible Diels-Alder furan/maleimide polymer networks as function of crosslink density Macromol. Chem. Phys. 213 2012 157 165 10.1002/macp.201100405
-
(2012)
Macromol. Chem. Phys.
, vol.213
, pp. 157-165
-
-
Toncelli, C.1
De Reus, D.C.2
Picchioni, F.3
Broekhuis, A.A.4
-
153
-
-
84888362584
-
Green chemistry for the synthesis of methacrylate-based hydrogels crosslinked through Diels-Alder reaction
-
C. García-Astrain, A. Gandini, D. Coelho, I. Mondragon, A. Retegi, A. Eceiza, and et al. Green chemistry for the synthesis of methacrylate-based hydrogels crosslinked through Diels-Alder reaction Eur. Polym. J. 49 2013 3998 4007 10.1016/j.eurpolymj.2013.09.004
-
(2013)
Eur. Polym. J.
, vol.49
, pp. 3998-4007
-
-
García-Astrain, C.1
Gandini, A.2
Coelho, D.3
Mondragon, I.4
Retegi, A.5
Eceiza, A.6
-
154
-
-
79959265875
-
Direct synthesis of biodegradable polysaccharide derivative hydrogels through aqueous Diels-Alder chemistry
-
H. Tan, J.P. Rubin, and K.G. Marra Direct synthesis of biodegradable polysaccharide derivative hydrogels through aqueous Diels-Alder chemistry Macromol. Rapid Commun. 32 2011 905 911 10.1002/marc.201100125
-
(2011)
Macromol. Rapid Commun.
, vol.32
, pp. 905-911
-
-
Tan, H.1
Rubin, J.P.2
Marra, K.G.3
-
155
-
-
84883311793
-
Investigation of the Diels-Alder reaction as a cross-linking mechanism for degradable poly(ethylene glycol) based hydrogels
-
S. Kirchhof, F.P. Brandl, N. Hammer, and A.M. Goepferich Investigation of the Diels-Alder reaction as a cross-linking mechanism for degradable poly(ethylene glycol) based hydrogels J. Mater. Chem. B 1 2013 4855 4864 10.1039/c3tb20831a
-
(2013)
J. Mater. Chem. B
, vol.1
, pp. 4855-4864
-
-
Kirchhof, S.1
Brandl, F.P.2
Hammer, N.3
Goepferich, A.M.4
-
156
-
-
84918773058
-
New insights into the cross-linking and degradation mechanism of Diels-Alder hydrogels
-
S. Kirchhof, A. Strasser, H.-J. Wittmann, V. Messmann, N. Hammer, A.M. Goepferich, and et al. New insights into the cross-linking and degradation mechanism of Diels-Alder hydrogels J. Mater. Chem. B 3 2015 449 457 10.1039/C4TB01680G
-
(2015)
J. Mater. Chem. B
, vol.3
, pp. 449-457
-
-
Kirchhof, S.1
Strasser, A.2
Wittmann, H.-J.3
Messmann, V.4
Hammer, N.5
Goepferich, A.M.6
-
157
-
-
84880328510
-
A novel bioabsorbable gel formed from a mixed micelle solution of poly(oxyethylene)-block-poly(L-lactide) and poly(oxyethylene)-block-poly(D-lactide) by concomitant stereocomplexation and chain extension
-
Y.-I. Hsu, K. Masutani, Y. Kimura, and T. Yamaoka A novel bioabsorbable gel formed from a mixed micelle solution of poly(oxyethylene)-block-poly(L-lactide) and poly(oxyethylene)-block-poly(D-lactide) by concomitant stereocomplexation and chain extension Macromol. Chem. Phys. 214 2013 1559 1568 10.1002/macp.201300230
-
(2013)
Macromol. Chem. Phys.
, vol.214
, pp. 1559-1568
-
-
Hsu, Y.-I.1
Masutani, K.2
Kimura, Y.3
Yamaoka, T.4
-
158
-
-
77951936291
-
Fabrication of maleimide containing thiol reactive hydrogels via Diels-Alder/retro-Diels-Alder strategy
-
I. Kosif, E.-J. Park, R. Sanyal, and A. Sanyal Fabrication of maleimide containing thiol reactive hydrogels via Diels-Alder/retro-Diels-Alder strategy Macromolecules 43 2010 4140 4148 10.1021/ma100396c
-
(2010)
Macromolecules
, vol.43
, pp. 4140-4148
-
-
Kosif, I.1
Park, E.-J.2
Sanyal, R.3
Sanyal, A.4
-
159
-
-
33749557616
-
Rational design of hydrogels for tissue engineering: Impact of physical factors on cell behavior
-
F.P. Brandl, F. Sommer, and A.M. Goepferich Rational design of hydrogels for tissue engineering: impact of physical factors on cell behavior Biomaterials 28 2007 134 146 10.1016/j.biomaterials.2006.09.017
-
(2007)
Biomaterials
, vol.28
, pp. 134-146
-
-
Brandl, F.P.1
Sommer, F.2
Goepferich, A.M.3
-
160
-
-
79955412522
-
Diels-Alder click cross-linked hyaluronic acid hydrogels for tissue engineering
-
C.M. Nimmo, S.C. Owen, and M.S. Shoichet Diels-Alder click cross-linked hyaluronic acid hydrogels for tissue engineering Biomacromolecules 12 2011 824 830 10.1021/bm101446k
-
(2011)
Biomacromolecules
, vol.12
, pp. 824-830
-
-
Nimmo, C.M.1
Owen, S.C.2
Shoichet, M.S.3
-
161
-
-
84879181309
-
Hyaluronic acid click hydrogels emulate the extracellular matrix
-
S.C. Owen, S.A. Fisher, R.Y. Tam, C.M. Nimmo, and M.S. Shoichet Hyaluronic acid click hydrogels emulate the extracellular matrix Langmuir 29 2013 7393 7400 10.1021/la305000w
-
(2013)
Langmuir
, vol.29
, pp. 7393-7400
-
-
Owen, S.C.1
Fisher, S.A.2
Tam, R.Y.3
Nimmo, C.M.4
Shoichet, M.S.5
-
162
-
-
84891434679
-
An injectable hyaluronic acid/PEG hydrogel for cartilage tissue engineering formed by integrating enzymatic crosslinking and Diels-Alder "click chemistry"
-
F. Yu, X. Cao, Y. Li, L. Zeng, B. Yuan, and X. Chen An injectable hyaluronic acid/PEG hydrogel for cartilage tissue engineering formed by integrating enzymatic crosslinking and Diels-Alder "click chemistry" Polym. Chem. 5 2014 1082 1090 10.1039/c3py00869j
-
(2014)
Polym. Chem.
, vol.5
, pp. 1082-1090
-
-
Yu, F.1
Cao, X.2
Li, Y.3
Zeng, L.4
Yuan, B.5
Chen, X.6
-
163
-
-
84878248642
-
An interpenetrating HA/G/CS biomimic hydrogel via Diels-Alder click chemistry for cartilage tissue engineering
-
F. Yu, X. Cao, L. Zeng, Q. Zhang, and X. Chen An interpenetrating HA/G/CS biomimic hydrogel via Diels-Alder click chemistry for cartilage tissue engineering Carbohydr. Polym. 97 2013 188 195 10.1016/j.carbpol.2013.04.046
-
(2013)
Carbohydr. Polym.
, vol.97
, pp. 188-195
-
-
Yu, F.1
Cao, X.2
Zeng, L.3
Zhang, Q.4
Chen, X.5
-
164
-
-
84863581418
-
The effects of peptide modified gellan gum and olfactory ensheathing glia cells on neural stem/progenitor cell fate
-
N.A. Silva, M.J. Cooke, R.Y. Tam, N. Sousa, A.J. Salgado, R.L. Reis, and et al. The effects of peptide modified gellan gum and olfactory ensheathing glia cells on neural stem/progenitor cell fate Biomaterials 33 2012 6345 6354 10.1016/j.biomaterials.2012.05.050
-
(2012)
Biomaterials
, vol.33
, pp. 6345-6354
-
-
Silva, N.A.1
Cooke, M.J.2
Tam, R.Y.3
Sousa, N.4
Salgado, A.J.5
Reis, R.L.6
-
165
-
-
84875974442
-
Synthetically tractable click hydrogels for three-dimensional cell culture formed using tetrazine-norbornene chemistry
-
D.L. Alge, M.A. Azagarsamy, D.F. Donohue, and K.S. Anseth Synthetically tractable click hydrogels for three-dimensional cell culture formed using tetrazine-norbornene chemistry Biomacromolecules 14 2013 949 953 10.1021/bm4000508
-
(2013)
Biomacromolecules
, vol.14
, pp. 949-953
-
-
Alge, D.L.1
Azagarsamy, M.A.2
Donohue, D.F.3
Anseth, K.S.4
-
166
-
-
84873666390
-
Diels-Alder mediated controlled release from a poly(ethylene glycol) based hydrogel
-
K.C. Koehler, K.S. Anseth, and C.N. Bowman Diels-Alder mediated controlled release from a poly(ethylene glycol) based hydrogel Biomacromolecules 14 2013 538 547 10.1021/bm301789d
-
(2013)
Biomacromolecules
, vol.14
, pp. 538-547
-
-
Koehler, K.C.1
Anseth, K.S.2
Bowman, C.N.3
-
167
-
-
84874952972
-
A Diels-Alder modulated approach to control and sustain the release of dexamethasone and induce osteogenic differentiation of human mesenchymal stem cells
-
K.C. Koehler, D.L. Alge, K.S. Anseth, and C.N. Bowman A Diels-Alder modulated approach to control and sustain the release of dexamethasone and induce osteogenic differentiation of human mesenchymal stem cells Biomaterials 34 2013 4150 4158 10.1016/j.biomaterials.2013.02.020
-
(2013)
Biomaterials
, vol.34
, pp. 4150-4158
-
-
Koehler, K.C.1
Alge, D.L.2
Anseth, K.S.3
Bowman, C.N.4
-
168
-
-
0012005469
-
The roles of changes in bonding vs. Packing fraction in the pressure-induced acceleration of the Diels-Alder reaction
-
R.A. Firestone, and G.M. Smith The roles of changes in bonding vs. packing fraction in the pressure-induced acceleration of the Diels-Alder reaction Chem. Ber. 122 1989 1089 1094 10.1002/cber.19891220614
-
(1989)
Chem. Ber.
, vol.122
, pp. 1089-1094
-
-
Firestone, R.A.1
Smith, G.M.2
-
169
-
-
37049067073
-
The kinetic effects of water and of cyclodextrins on Diels-Alder reactions. Host-guest chemistry. Part 18
-
N.K. Sangwan, and H.-J. Schneider The kinetic effects of water and of cyclodextrins on Diels-Alder reactions. Host-guest chemistry. Part 18 J. Chem. Soc. Perkin Trans. 2 1989 1223 1227 10.1039/p29890001223
-
(1989)
J. Chem. Soc. Perkin Trans.
, vol.2
, pp. 1223-1227
-
-
Sangwan, N.K.1
Schneider, H.-J.2
-
170
-
-
84865517099
-
Using light and a molecular switch to 'lock' and 'unlock' the Diels-Alder reaction
-
Z. Erno, A.M. Asadirad, V. Lemieux, and N.R. Branda Using light and a molecular switch to 'lock' and 'unlock' the Diels-Alder reaction Org. Biomol. Chem. 10 2012 2787 10.1039/c2ob06908c
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 2787
-
-
Erno, Z.1
Asadirad, A.M.2
Lemieux, V.3
Branda, N.R.4
-
171
-
-
84857445877
-
Genetically encoded norbornene directs site-specific cellular protein labelling via a rapid bioorthogonal reaction
-
K. Lang, L. Davis, J. Torres-Kolbus, C. Chou, A. Deiters, and J.W. Chin Genetically encoded norbornene directs site-specific cellular protein labelling via a rapid bioorthogonal reaction Nat. Chem. 4 2012 298 304 10.1038/nchem.1250
-
(2012)
Nat. Chem.
, vol.4
, pp. 298-304
-
-
Lang, K.1
Davis, L.2
Torres-Kolbus, J.3
Chou, C.4
Deiters, A.5
Chin, J.W.6
-
172
-
-
84863443015
-
Genetic encoding of bicyclononynes and trans-cyclooctenes for site-specific protein labeling in vitro and in live mammalian cells via rapid fluorogenic Diels-Alder reactions
-
K. Lang, L. Davis, S. Wallace, M. Mahesh, D.J. Cox, M.L. Blackman, and et al. Genetic encoding of bicyclononynes and trans-cyclooctenes for site-specific protein labeling in vitro and in live mammalian cells via rapid fluorogenic Diels-Alder reactions J. Am. Chem. Soc. 134 2012 10317 10320 10.1021/ja302832g
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 10317-10320
-
-
Lang, K.1
Davis, L.2
Wallace, S.3
Mahesh, M.4
Cox, D.J.5
Blackman, M.L.6
-
173
-
-
84860174738
-
A genetically encoded norbornene amino acid for the mild and selective modification of proteins in a copper-free click reaction
-
E. Kaya, M. Vrabel, C. Deiml, S. Prill, V.S. Fluxa, and T. Carell A genetically encoded norbornene amino acid for the mild and selective modification of proteins in a copper-free click reaction Angew. Chem. Int. Ed. 51 2012 4466 4469 10.1002/anie.201109252
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 4466-4469
-
-
Kaya, E.1
Vrabel, M.2
Deiml, C.3
Prill, S.4
Fluxa, V.S.5
Carell, T.6
-
174
-
-
84876470032
-
Red-light-controlled protein-RNA crosslinking with a genetically encoded furan
-
M.J. Schmidt, and D. Summerer Red-light-controlled protein-RNA crosslinking with a genetically encoded furan Angew. Chem. Int. Ed. 52 2013 4690 4693 10.1002/anie.201300754
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 4690-4693
-
-
Schmidt, M.J.1
Summerer, D.2
-
176
-
-
0014687516
-
Modification of lysine and arginine residues of lysozyme and the effect of enzymatic activity
-
R.C. Davies, and A. Neuberger Modification of lysine and arginine residues of lysozyme and the effect of enzymatic activity BBA - Enzymol. 178 1969 306 317 10.1016/0005-2744(69)90398-2
-
(1969)
BBA - Enzymol.
, vol.178
, pp. 306-317
-
-
Davies, R.C.1
Neuberger, A.2
-
177
-
-
0017252056
-
Effect of succinylation (3-carboxypropionylation) on the conformation and immunological activity of ovalbumin
-
S.A. Kidwai, A.A. Ansari, and A. Salahuddin Effect of succinylation (3-carboxypropionylation) on the conformation and immunological activity of ovalbumin Biochem. J. 155 1976 171 180
-
(1976)
Biochem. J.
, vol.155
, pp. 171-180
-
-
Kidwai, S.A.1
Ansari, A.A.2
Salahuddin, A.3
-
178
-
-
49349118175
-
Changes in conformation and immunological activity of ovalbumin during its modification with different acid anhydrides
-
M. Abul Qasim, and A. Salahuddin Changes in conformation and immunological activity of ovalbumin during its modification with different acid anhydrides BBA - Protein, Structure 536 1978 50 63 10.1016/0005-2795(78)90050-8
-
(1978)
BBA - Protein, Structure
, vol.536
, pp. 50-63
-
-
Abul Qasim, M.1
Salahuddin, A.2
-
179
-
-
0029671190
-
Acylation of the α-amino group in neuropeptide Y(12-36) increases binding affinity for the Y2 receptor
-
S. Murase, N. Yumoto, M.G. Petukhov, and S. Yoshikawa Acylation of the α-amino group in neuropeptide Y(12-36) increases binding affinity for the Y2 receptor J. Biochem. 119 1996 37 41
-
(1996)
J. Biochem.
, vol.119
, pp. 37-41
-
-
Murase, S.1
Yumoto, N.2
Petukhov, M.G.3
Yoshikawa, S.4
-
180
-
-
22844450329
-
Effects of chemical modification of lysine residues on the sweetness of lysozyme
-
T. Masuda, N. Ide, and N. Kitabatake Effects of chemical modification of lysine residues on the sweetness of lysozyme Chem. Senses 30 2005 253 264 10.1093/chemse/bji021
-
(2005)
Chem. Senses
, vol.30
, pp. 253-264
-
-
Masuda, T.1
Ide, N.2
Kitabatake, N.3
-
181
-
-
78649832816
-
Conjugation of methacrylamide groups to a model protein via a reducible linker for immobilization and subsequent triggered release from hydrogels
-
E. Verheyen, L. Delain-Bioton, S. van der Wal, N. el Morabit, A. Barendregt, W.E. Hennink, and et al. Conjugation of methacrylamide groups to a model protein via a reducible linker for immobilization and subsequent triggered release from hydrogels Macromol. Biosci. 10 2010 1517 1526 10.1002/mabi.201000168
-
(2010)
Macromol. Biosci.
, vol.10
, pp. 1517-1526
-
-
Verheyen, E.1
Delain-Bioton, L.2
Van Der Wal, S.3
El Morabit, N.4
Barendregt, A.5
Hennink, W.E.6
-
182
-
-
84924086510
-
Protein compatibility of selected cross-linking reactions for hydrogels
-
N. Hammer, F.P. Brandl, S. Kirchhof, V. Messmann, and A.M. Goepferich Protein compatibility of selected cross-linking reactions for hydrogels Macromol. Biosci. 15 2015 405 413 10.1002/mabi.201400379
-
(2015)
Macromol. Biosci.
, vol.15
, pp. 405-413
-
-
Hammer, N.1
Brandl, F.P.2
Kirchhof, S.3
Messmann, V.4
Goepferich, A.M.5
-
183
-
-
41549148288
-
Hydrogels in drug delivery: Progress and challenges
-
T.R. Hoare, and D.S. Kohane Hydrogels in drug delivery: progress and challenges Polymer 49 2008 1993 2007 10.1016/j.polymer.2008.01.027
-
(2008)
Polymer
, vol.49
, pp. 1993-2007
-
-
Hoare, T.R.1
Kohane, D.S.2
-
184
-
-
60149111910
-
PEG hydrogels for the controlled release of biomolecules in regenerative medicine
-
C.-C. Lin, and K.S. Anseth PEG hydrogels for the controlled release of biomolecules in regenerative medicine Pharm. Res. 26 2009 631 643 10.1007/s11095-008-9801-2
-
(2009)
Pharm. Res.
, vol.26
, pp. 631-643
-
-
Lin, C.-C.1
Anseth, K.S.2
-
185
-
-
0141567459
-
Physical stability of proteins in aqueous solution: Mechanism and driving forces in nonnative protein aggregation
-
E.Y. Chi, S. Krishnan, T.W. Randolph, and J.F. Carpenter Physical stability of proteins in aqueous solution: mechanism and driving forces in nonnative protein aggregation Pharm. Res. 20 2003 1325 1336 10.1023/A:1025771421906
-
(2003)
Pharm. Res.
, vol.20
, pp. 1325-1336
-
-
Chi, E.Y.1
Krishnan, S.2
Randolph, T.W.3
Carpenter, J.F.4
-
186
-
-
33846140780
-
Antibody structure, instability, and formulation
-
W. Wang, S. Singh, D.L. Zeng, K. King, and S. Nema Antibody structure, instability, and formulation J. Pharm. Sci. 96 2006 1 26 10.1002/jps.20727
-
(2006)
J. Pharm. Sci.
, vol.96
, pp. 1-26
-
-
Wang, W.1
Singh, S.2
Zeng, D.L.3
King, K.4
Nema, S.5
-
187
-
-
84858375997
-
Accurate prediction of rate constants of Diels-Alder reactions and application to design of Diels-Alder ligation
-
S.-Y. Tang, J. Shi, and Q.-X. Guo Accurate prediction of rate constants of Diels-Alder reactions and application to design of Diels-Alder ligation Org. Biomol. Chem. 10 2012 2673 2682 10.1039/C2OB07079K
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 2673-2682
-
-
Tang, S.-Y.1
Shi, J.2
Guo, Q.-X.3
|