-
3
-
-
0027480532
-
Controlling cell chemistry with caged compounds
-
United States
-
S. R. Adams and R. Y. Tsien, Controlling cell chemistry with caged compounds, in Annual Review of Physiology, United States, 1993, vol. 55, pp. 755–784.
-
(1993)
Annual Review of Physiology
, vol.55
, pp. 755-784
-
-
Adams, S.R.1
Tsien, R.Y.2
-
4
-
-
0036007052
-
Photolabile protecting groups and linkers
-
C. G. Bochet Photolabile protecting groups and linkers J. Chem. Soc., Perkin Trans. 1 2002 125-142.
-
(2002)
J. Chem. Soc., Perkin Trans. 1
, pp. 125-142
-
-
Bochet, C.G.1
-
5
-
-
0000576453
-
Photoremovable Protecting Groups: Mechanisms and Applications
-
A. P. Pelliccioli J. Wirz Photoremovable Protecting Groups: Mechanisms and Applications Photochem. Photobiol. Sci. 2002 1 441-458.
-
(2002)
Photochem. Photobiol. Sci.
, vol.1
, pp. 441-458
-
-
Pelliccioli, A.P.1
Wirz, J.2
-
7
-
-
0034203977
-
New Phototriggers: Extending the p-Hydroxyphenacyl π-π* Absorption Range
-
P. G. Conrad R. S. Givens J. F. W. Weber K. Kandler New Phototriggers: Extending the p-Hydroxyphenacyl π-π* Absorption Range Org. Lett. 2000 2 1545-1547.
-
(2000)
Org. Lett.
, vol.2
, pp. 1545-1547
-
-
Conrad, P.G.1
Givens, R.S.2
Weber, J.F.W.3
Kandler, K.4
-
9
-
-
0030755239
-
New Photoactivated Protecting Groups. 7. p-Hydroxyphenacyl: A Phototrigger for Excitatory Amino Acids and Peptides
-
R. S. Givens A. Jung C. H. Park J. Weber W. Bartlett New Photoactivated Protecting Groups. 7. p-Hydroxyphenacyl: A Phototrigger for Excitatory Amino Acids and Peptides J. Am. Chem. Soc. 1997 119 8369-8370.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 8369-8370
-
-
Givens, R.S.1
Jung, A.2
Park, C.H.3
Weber, J.4
Bartlett, W.5
-
10
-
-
0030603031
-
P-Hydroxyphenacyl ATP: A New Phototrigger
-
R. S. Givens C. H. Park p-Hydroxyphenacyl ATP: A New Phototrigger Tetrahedron Lett. 1996 37 6259-6262.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 6259-6262
-
-
Givens, R.S.1
Park, C.H.2
-
12
-
-
0030907953
-
New Photoactivated Protecting Groups. 6. p-Hydroxyphenacyl: A Phototrigger for Chemical and Biochemical Probes
-
C. H. Park R. S. Givens New Photoactivated Protecting Groups. 6. p-Hydroxyphenacyl: A Phototrigger for Chemical and Biochemical Probes J. Am. Chem. Soc. 1997 119 2453-2463.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 2453-2463
-
-
Park, C.H.1
Givens, R.S.2
-
13
-
-
0001489322
-
Direct Photolysis of Phenacyl Protecting Groups Studied by Laser Flash Photolysis: An Excited State Hydrogen Atom Abstraction Pathway Leads to Formation of Carboxylic Acids and acetophenone
-
A. Banerjee D. E. Falvey Direct Photolysis of Phenacyl Protecting Groups Studied by Laser Flash Photolysis: An Excited State Hydrogen Atom Abstraction Pathway Leads to Formation of Carboxylic Acids and acetophenone J. Am. Chem. Soc. 1998 120 2965-2966.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 2965-2966
-
-
Banerjee, A.1
Falvey, D.E.2
-
14
-
-
0001238134
-
Protecting Groups that Can Be Removed through Photochemical Electron Transfer: Mechanistic and Product Studies on Photosensitized Release of Carboxylates from Phenacyl Esters
-
A. Banerjee D. E. Falvey Protecting Groups that Can Be Removed through Photochemical Electron Transfer: Mechanistic and Product Studies on Photosensitized Release of Carboxylates from Phenacyl Esters J. Org. Chem. 1997 62 6245-6251.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6245-6251
-
-
Banerjee, A.1
Falvey, D.E.2
-
15
-
-
0033615751
-
Photoreleasable Protecting Groups Based on Electron Transfer Chemistry. Donor Sensitized Release of Phenacyl Groups from Alcohols, Phosphates and Diacids
-
A. Banerjee K. Lee D. E. Falvey Photoreleasable Protecting Groups Based on Electron Transfer Chemistry. Donor Sensitized Release of Phenacyl Groups from Alcohols, Phosphates and Diacids Tetrahedron 1999 55 12699-12710.
-
(1999)
Tetrahedron
, vol.55
, pp. 12699-12710
-
-
Banerjee, A.1
Lee, K.2
Falvey, D.E.3
-
16
-
-
0032565843
-
Protecting Group Release through Photoinduced Electron Transfer: Wavelength Control through Sensitized Irradiation
-
A. Banerjee K. Lee Q. Yu A. G. Fang D. E. Falvey Protecting Group Release through Photoinduced Electron Transfer: Wavelength Control through Sensitized Irradiation Tetrahedron Lett. 1998 39 4635-4638.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 4635-4638
-
-
Banerjee, A.1
Lee, K.2
Yu, Q.3
Fang, A.G.4
Falvey, D.E.5
-
17
-
-
0034605471
-
Photochemically Removable Protecting Groups Based on Covalently Linked Electron Donor-Acceptor Systems
-
K. Lee D. E. Falvey Photochemically Removable Protecting Groups Based on Covalently Linked Electron Donor-Acceptor Systems J. Am. Chem. Soc. 2000 122 9361-9366.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 9361-9366
-
-
Lee, K.1
Falvey, D.E.2
-
18
-
-
0442295210
-
2,5-Dimethylphenacyl as a New Photoreleasable Protecting Group for Carboxylic Acids
-
P. Klán M. Zabadal D. Heger 2,5-Dimethylphenacyl as a New Photoreleasable Protecting Group for Carboxylic Acids Org. Lett. 2000 2 1569-1571.
-
(2000)
Org. Lett.
, vol.2
, pp. 1569-1571
-
-
Klán, P.1
Zabadal, M.2
Heger, D.3
-
19
-
-
0035892201
-
2,5-Dimethylphenacyl Esters: A Photoremovable Protecting Group for Carboxylic Acids
-
M. Zabadal A. P. Pelliccioli P. Klán J. Wirz 2,5-Dimethylphenacyl Esters: A Photoremovable Protecting Group for Carboxylic Acids J. Phys. Chem. A. 2001 105 10329-10333.
-
(2001)
J. Phys. Chem. A.
, vol.105
, pp. 10329-10333
-
-
Zabadal, M.1
Pelliccioli, A.P.2
Klán, P.3
Wirz, J.4
-
21
-
-
0009187886
-
Enolate Structures Contributing to the Transition State for Nucleophilic Substitution an α-Substituted Carbonyl Compounds
-
T. I. Yousaf E. S. Lewis Enolate Structures Contributing to the Transition State for Nucleophilic Substitution an α-Substituted Carbonyl Compounds J. Am. Chem. Soc. 1987 109 6137-6142.
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 6137-6142
-
-
Yousaf, T.I.1
Lewis, E.S.2
-
22
-
-
0036329835
-
Photolysis of Phenacyl esters in a Two-Phase System
-
R. Ruzicka M. Zabadal P. Klán Photolysis of Phenacyl esters in a Two-Phase System Synth. Commun. 2002 32 2581-2590.
-
(2002)
Synth. Commun.
, vol.32
, pp. 2581-2590
-
-
Ruzicka, R.1
Zabadal, M.2
Klán, P.3
-
23
-
-
0000315935
-
Type II Photoprocesses of Phenyl Ketones. Procedures for Determining Meaningful Quantum Yields and Triplet Lifetimes
-
P. J. Wagner I. E. Kochevar A. E. Kemppainen Type II Photoprocesses of Phenyl Ketones. Procedures for Determining Meaningful Quantum Yields and Triplet Lifetimes J. Am. Chem. Soc 1972 94 7489-7494.
-
(1972)
J. Am. Chem. Soc
, vol.94
, pp. 7489-7494
-
-
Wagner, P.J.1
Kochevar, I.E.2
Kemppainen, A.E.3
-
24
-
-
0001331615
-
Photoenolisation
-
P. G. Sammes Photoenolisation Tetrahedron 1976 32 405-422.
-
(1976)
Tetrahedron
, vol.32
, pp. 405-422
-
-
Sammes, P.G.1
-
25
-
-
33847799902
-
A Rotation-Controlled Exctited-State Reaction. The Photoenolization of Ortho Alkyl Phenyl Ketones
-
P. J. Wagner C.-P. Chen A Rotation-Controlled Exctited-State Reaction. The Photoenolization of Ortho Alkyl Phenyl Ketones J. Am. Chem. Soc. 1976 98 239-241.
-
(1976)
J. Am. Chem. Soc.
, vol.98
, pp. 239-241
-
-
Wagner, P.J.1
Chen, C.-P.2
-
26
-
-
0001637399
-
The Photoenolization of 2-Methylacetophenone and Related Compounds
-
R. Haag J. Wirz P. J. Wagner The Photoenolization of 2-Methylacetophenone and Related Compounds Helv. Chim. Acta 1977 60 2595-2607.
-
(1977)
Helv. Chim. Acta
, vol.60
, pp. 2595-2607
-
-
Haag, R.1
Wirz, J.2
Wagner, P.J.3
-
27
-
-
0001047474
-
Photolysis of α-Chloro-o-methylacetophenones
-
W. R. Bergmark Photolysis of α-Chloro-o-methylacetophenones J. Chem. Soc., Chem. Commun. 1978 61-62.
-
(1978)
J. Chem. Soc., Chem. Commun.
, pp. 61-62
-
-
Bergmark, W.R.1
-
28
-
-
0001333635
-
A Laser Flash Photolysis Study of the Mechanism of the Photocyclization of α-Chloro-o-methylacetophenones
-
J. C. Netto-Ferreira J. C. Scaiano A Laser Flash Photolysis Study of the Mechanism of the Photocyclization of α-Chloro-o-methylacetophenones J. Am. Chem. Soc. 1991 113 5800-5803.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 5800-5803
-
-
Netto-Ferreira, J.C.1
Scaiano, J.C.2
-
29
-
-
0034807924
-
Photorelease of HCl from o-Methylphenacyl Chloride Proceeds through the Z-Xylylenol
-
A. P. Pelliccioli P. Klán M. Zabadal J. Wirz Photorelease of HCl from o-Methylphenacyl Chloride Proceeds through the Z-Xylylenol J. Am. Chem. Soc. 2001 123 7931-7932.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7931-7932
-
-
Pelliccioli, A.P.1
Klán, P.2
Zabadal, M.3
Wirz, J.4
-
30
-
-
0001740035
-
Photochemistry of Phosphate Esters: An efficient Method for the Generation of Electrophiles
-
R. S. Givens B. Matuszewski Photochemistry of Phosphate Esters: An efficient Method for the Generation of Electrophiles J. Am. Chem. Soc. 1984 106 6860-6861.
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 6860-6861
-
-
Givens, R.S.1
Matuszewski, B.2
-
31
-
-
1542532022
-
Photochemistry of Phosphate Esters
-
R. S. Givens L. W. Kueper Photochemistry of Phosphate Esters Chem. Rev. 1993 93 55-66.
-
(1993)
Chem. Rev.
, vol.93
, pp. 55-66
-
-
Givens, R.S.1
Kueper, L.W.2
-
32
-
-
0030907953
-
New Photoactivated Protecting Groups. 6. p-Hydroxyphenacyl: A Phototrigger for Chemical and Biochemical Probes
-
C.-H. Park R. S. Givens New Photoactivated Protecting Groups. 6. p-Hydroxyphenacyl: a Phototrigger for Chemical and Biochemical Probes J. Am. Chem. Soc. 1997 119 2453-2463.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 2453-2463
-
-
Park, C.-H.1
Givens, R.S.2
-
33
-
-
0032783950
-
Deactivation Behavior and Excited-State Properties of (Coumarin-4-yl)methyl Derivatives. 1. Photocleavage of (7-Methoxycoumarin-4-yl)methyl Caged Acids with Fluorescence Enhancement
-
B. Schade V. Hagen R. Schmidt R. Herbrich E. Krause T. Eckardt J. Bendig Deactivation Behavior and Excited-State Properties of (Coumarin-4-yl)methyl Derivatives. 1. Photocleavage of (7-Methoxycoumarin-4-yl)methyl Caged Acids with Fluorescence Enhancement J. Org. Chem. 1999 64 9109-9117.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 9109-9117
-
-
Schade, B.1
Hagen, V.2
Schmidt, R.3
Herbrich, R.4
Krause, E.5
Eckardt, T.6
Bendig, J.7
-
34
-
-
0033950581
-
Kinetics and Mechanism of Phosphate Photorelease from Benzoin Diethyl Phosphate: Evidence for Adiabatic Fission to an α-Keto Cation in the Triplet State
-
C. S. Rajesh R. S. Givens J. Wirz Kinetics and Mechanism of Phosphate Photorelease from Benzoin Diethyl Phosphate: Evidence for Adiabatic Fission to an α-Keto Cation in the Triplet State J. Am. Chem. Soc. 2000 122 611-618.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 611-618
-
-
Rajesh, C.S.1
Givens, R.S.2
Wirz, J.3
-
36
-
-
0033392836
-
Synthesis, Photochemistry and Application of (7-Methoxycoumarin-4-yl) Methyl-Caged 8-Bromoadenosine Cyclic 3′,5′-Monophosphate and 8-Bromoguanosine Cyclic 3′,5′-Monophosphate Photolyzed in the Nanosecond Time Region
-
V. Hagen J. Bendig S. Frings B. Wiesner B. Schade S. Helm D. Lorenz U. B. Kaupp Synthesis, Photochemistry and Application of (7-Methoxycoumarin-4-yl) Methyl-Caged 8-Bromoadenosine Cyclic 3′,5′-Monophosphate and 8-Bromoguanosine Cyclic 3′,5′-Monophosphate Photolyzed in the Nanosecond Time Region J. Photochem. Photobiol., B 1999 53 91-102.
-
(1999)
J. Photochem. Photobiol., B
, vol.53
, pp. 91-102
-
-
Hagen, V.1
Bendig, J.2
Frings, S.3
Wiesner, B.4
Schade, B.5
Helm, S.6
Lorenz, D.7
Kaupp, U.B.8
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