메뉴 건너뛰기




Volumn , Issue , 2003, Pages 69-1-69-46

Photoremovable protecting groups

Author keywords

[No Author keywords available]

Indexed keywords


EID: 70450182428     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (18)

References (91)
  • 1
    • 0017867017 scopus 로고
    • Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: Utilization by the Na: Pump of human red blood cell ghosts
    • Kaplan, J. H., Forbush, B. I., and Hoffman, J. F., Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: utilization by the Na: pump of human red blood cell ghosts, Biochemistry, 17, 1929-1935, 1978.
    • (1978) Biochemistry , vol.17 , pp. 1929-1935
    • Kaplan, J.H.1    Forbush, B.I.2    Hoffman, J.F.3
  • 2
    • 0017684571 scopus 로고
    • Synthesis, structure, and reactivity of adenosine cyclic 3',5'-phosphate benzyl triesters
    • Engels, J. and Schlaeger, E.-J., Synthesis, structure, and reactivity of adenosine cyclic 3',5'-phosphate benzyl triesters, J. Med. Chem., 20, 907-911, 1977.
    • (1977) J. Med. Chem , vol.20 , pp. 907-911
    • Engels, J.1    Schlaeger, E.-J.2
  • 3
    • 1542532022 scopus 로고
    • Photochemistry of phosphate esters
    • Givens, R. S. and Kueper III, L. W., Photochemistry of phosphate esters, Chem. Rev., 93, 55-66, 1993.
    • (1993) Chem. Rev , vol.93 , pp. 55-66
    • Givens, R.S.1    Kueper, L.W.2
  • 4
    • 4544276629 scopus 로고    scopus 로고
    • Controlling cell chemistry with caged compounds
    • Adams, S. R. and Tsien, R. Y., Controlling cell chemistry with caged compounds, Ann. Rev. Physiol., 18, 755-784, 2000.
    • (2000) Ann. Rev. Physiol , vol.18 , pp. 755-784
    • Adams, S.R.1    Tsien, R.Y.2
  • 5
    • 0347861614 scopus 로고
    • Synthetic, mechanistic and photochemical studies of phosphate esters of substituted benzoins
    • Corrie, J. E. T. and Trentham, D. R., Synthetic, mechanistic and photochemical studies of phosphate esters of substituted benzoins, J. Chem. Soc., Perkin Trans. 1, 2409-2417, 1992.
    • (1992) J. Chem. Soc., Perkin Trans , vol.1 , pp. 2409-2417
    • Corrie, J.E.T.1    Trentham, D.R.2
  • 6
    • 0000576453 scopus 로고    scopus 로고
    • Photoremovable-protecting groups: Reaction mechanism and applications
    • Pelliccioli, A. P. and Wirz, J., Photoremovable-protecting groups: reaction mechanism and applications, Photochem. Photobiol. Sci., 1, 441-458, 2002.
    • (2002) Photochem. Photobiol. Sci , vol.1 , pp. 441-458
    • Pelliccioli, A.P.1    Wirz, J.2
  • 7
    • 0036007052 scopus 로고    scopus 로고
    • Photolabile protecting groups and linkers
    • Bochet, C. G., Photolabile protecting groups and linkers, J. Chem. Soc., Perkin Trans. 1, 125-142, 2002.
    • J. Chem. Soc., Perkin Trans , vol.1
    • Bochet, C.G.1
  • 8
    • 1342305811 scopus 로고    scopus 로고
    • The p-hydroxyphenacyl photoremovable protecting group
    • press
    • Givens, R. S. and Lee, J.-I., The p-hydroxyphenacyl photoremovable protecting group, J. Photosci., 2002, in press.
    • (2002) J. Photosci
    • Givens, R.S.1    Lee, J.-I.2
  • 10
    • 0037125492 scopus 로고    scopus 로고
    • Catalytic subunit of protein kinase caged at the activating phosphothreonine
    • Zou, K., Cheley, S., Givens, R. S., and Bayley, H., Catalytic subunit of protein kinase caged at the activating phosphothreonine, J. Am. Chem. Soc., 124, 8220-8229, 2002.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 8220-8229
    • Zou, K.1    Cheley, S.2    Givens, R.S.3    Bayley, H.4
  • 11
    • 0033516286 scopus 로고    scopus 로고
    • α-Haloacetophenone derivatives as photoreversible covalent inhibitors of protein tyrosine phosphates
    • Arabaci, G., Guo, X.-C., Beebe, K. D., Coggeshall, K. M., and Pei, D., α-Haloacetophenone derivatives as photoreversible covalent inhibitors of protein tyrosine phosphates, J. Am. Chem. Soc., 121, 5085-5086, 1999.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 5085-5086
    • Arabaci, G.1    Guo, X.-C.2    Beebe, K.D.3    Coggeshall, K.M.4    Pei, D.5
  • 13
    • 0001315370 scopus 로고
    • Phenacyl photosensitive blocking groups
    • Sheehan, J. C. and Umezawa, K., Phenacyl photosensitive blocking groups, J. Org. Chem., 38, 3771-3774, 1973.
    • (1973) J. Org. Chem , vol.38 , pp. 3771-3774
    • Sheehan, J.C.1    Umezawa, K.2
  • 15
    • 0031798357 scopus 로고    scopus 로고
    • New photoprotecting groups: Desyl and p-hydroxyphenacyl phosphate and carboxylate esters
    • Marriott, G., Ed., Academic Press, New York
    • Givens, R. S., Weber, J. F. W., Jung, A. H., and Park, C.-H., New photoprotecting groups: desyl and p-hydroxyphenacyl phosphate and carboxylate esters, in Methods in Enzymology, Vol. 291, Marriott, G., Ed., Academic Press, New York, 1998, 1-29.
    • (1998) Methods in Enzymology , vol.291 , pp. 1-29
    • Givens, R.S.1    Weber, J.F.W.2    Jung, A.H.3    Park, C.-H.4
  • 17
    • 0030979407 scopus 로고    scopus 로고
    • A photosensitive protecting group for amines based on coumarin chemistry
    • Wang, B. and Zheng, A., A photosensitive protecting group for amines based on coumarin chemistry, Chem. Pharm. Bull., 45, 715-718, 1997.
    • (1997) Chem. Pharm. Bull , vol.45 , pp. 715-718
    • Wang, B.1    Zheng, A.2
  • 18
    • 0001049630 scopus 로고
    • Photochemistry of enzyme-bound cinnamoyl derivatives
    • Koenigs, P. M., Faust, B. C., and Porter, N. A., Photochemistry of enzyme-bound cinnamoyl derivatives, J. Am. Chem. Soc., 115, 9371-9379, 1993.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 9371-9379
    • Koenigs, P.M.1    Faust, B.C.2    Porter, N.A.3
  • 19
    • 0020016226 scopus 로고
    • Physiological and pharmacological manipulations with light flashes
    • Lester, H. A. and Nerbonne, J. M., Physiological and pharmacological manipulations with light flashes, Ann. Rev. Biophys. Bioeng., 11, 151-175, 1982.
    • (1982) Ann. Rev. Biophys. Bioeng , vol.11 , pp. 151-175
    • Lester, H.A.1    Nerbonne, J.M.2
  • 21
    • 85056348601 scopus 로고
    • The photochemistry of unsaturated nitrocompounds. II. Relations among polarizability, reduction potential and photochemical behavior of some nitro compounds
    • Ried, V. W. and Wilk, M., The photochemistry of unsaturated nitrocompounds. II. Relations among polarizability, reduction potential and photochemical behavior of some nitro compounds, Justus Liebigs Ann. Chem., 590, 91-110, 1954.
    • (1954) Justus Liebigs Ann. Chem , vol.590 , pp. 91-110
    • Ried, V.W.1    Wilk, M.2
  • 22
    • 0026609631 scopus 로고
    • +2 on the kinetics of phosphate release in skeletal muscle
    • +2 on the kinetics of phosphate release in skeletal muscle, J. Biol. Chem., 267, 2459-2466, 1992.
    • (1992) J. Biol. Chem , vol.267 , pp. 2459-2466
    • Walker, J.W.1    Lu, Z.2    Moss, R.L.3
  • 23
    • 0026521097 scopus 로고
    • Mechanisms of cAMP-mediated relaxation of distal circular muscle in rabbit colon
    • Willenbucher, R. F., Xie, Y. N., Eysselein, V. E., and Snape, Jr., W. J., Mechanisms of cAMP-mediated relaxation of distal circular muscle in rabbit colon, Am. J. Physiol., 262, G159-G164, 1992.
    • (1992) Am. J. Physiol , vol.262 , pp. G159-G164
    • Willenbucher, R.F.1    Xie, Y.N.2    Eysselein, V.E.3    Snape, W.J.4
  • 24
    • 0025730795 scopus 로고
    • Rotational dynamics of spin-labeled F-actin during activation of myosin S1 ATPase using caged ATP
    • Ostap, E. M. and Thomas, D. D., Rotational dynamics of spin-labeled F-actin during activation of myosin S1 ATPase using caged ATP, Biophys. J., 59, 1235-1241, 1991.
    • (1991) Biophys. J , vol.59 , pp. 1235-1241
    • Ostap, E.M.1    Thomas, D.D.2
  • 25
    • 0033531730 scopus 로고    scopus 로고
    • DNA crosslinking by a phototriggered dehydromonocrotaline progenitor
    • Tepe, J. J. and Williams, R. M., DNA crosslinking by a phototriggered dehydromonocrotaline progenitor., J. Am. Chem. Soc., 121, 2951-2955, 1999.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 2951-2955
    • Tepe, J.J.1    Williams, R.M.2
  • 26
    • 33947483984 scopus 로고
    • Photolysis of desyl compounds: A new photolytic cyclization
    • Sheehan, J. C. and Wilson, R. M., Photolysis of desyl compounds: a new photolytic cyclization, J. Am. Chem. Soc., 86, 5277-5281, 1964.
    • (1964) J. Am. Chem. Soc , vol.86 , pp. 5277-5281
    • Sheehan, J.C.1    Wilson, R.M.2
  • 27
    • 0001740035 scopus 로고
    • Photochemistry of phosphate esters: An efficient method for the generation of electrophiles
    • Givens, R. S. and Matuszewski, B., Photochemistry of phosphate esters: an efficient method for the generation of electrophiles, J. Am. Chem. Soc., 106, 6860-6861, 1984.
    • (1984) J. Am. Chem. Soc , vol.106 , pp. 6860-6861
    • Givens, R.S.1    Matuszewski, B.2
  • 28
    • 0001267278 scopus 로고
    • Photochemistry of α-keto phosphate esters: Photorelease of a caged cAMP
    • Givens, R. S., Athey, P. S., Kueper, L. W. I., Matuszewski, B., and Xue, J.-Y., Photochemistry of α-keto phosphate esters: photorelease of a caged cAMP, J. Am. Chem. Soc., 114, 8708-8710, 1992.
    • (1992) J. Am. Chem. Soc , vol.114 , pp. 8708-8710
    • Givens, R.S.1    Athey, P.S.2    Kueper, L.W.I.3    Matuszewski, B.4    Xue, J.-Y.5
  • 29
    • 0000897083 scopus 로고
    • Photochemistry of phosphate esters: α-keto phosphates as a photoprotecting group for caged phosphate
    • Givens, R. S., Athey, P. S., Matuszewski, B., Kueper, L. W., Xue, J., and Fisher, T., Photochemistry of phosphate esters: α-keto phosphates as a photoprotecting group for caged phosphate, J. Am. Chem. Soc., 115, 6001-6012, 1993.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 6001-6012
    • Givens, R.S.1    Athey, P.S.2    Matuszewski, B.3    Kueper, L.W.4    Xue, J.5    Fisher, T.6
  • 30
    • 0001383523 scopus 로고
    • The photolysis of methoxy-substituted benzoin esters
    • Sheehan, J. C., Wilson, R. M., and Oxford, A. W., The photolysis of methoxy-substituted benzoin esters, J. Am. Chem. Soc., 93, 7222-7228, 1971.
    • (1971) J. Am. Chem. Soc , vol.93 , pp. 7222-7228
    • Sheehan, J.C.1    Wilson, R.M.2    Oxford, A.W.3
  • 31
    • 0033950581 scopus 로고    scopus 로고
    • Kinetics and mechanism of phosphate photorelease from benzoin diethyl phosphate: Evidence for adiabatic fission to an α-keto cation in the triplet state
    • Rajesh, C. S. Givens, R. S., and Wirz, J., 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., 122, 611-618, 2000.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 611-618
    • Rajesh, C.S.1    Givens, R.S.2    Wirz, J.3
  • 32
    • 37049090871 scopus 로고
    • p-Methoxyphenacyl esters as photodeblockable-protecting groups for phosphates
    • Epstein, W. W. and Garrossian, M., p-Methoxyphenacyl esters as photodeblockable-protecting groups for phosphates, J. Chem. Soc., Chem. Commun., 532-533, 1987.
    • (1987) J. Chem. Soc., Chem. Commun , pp. 532-533
    • Epstein, W.W.1    Garrossian, M.2
  • 33
    • 0030731319 scopus 로고    scopus 로고
    • Media controlled photo-Favorskii type rearrangement of α-chloro acetophenones: Synthesis of phenylacetic acids
    • Dhavale, D. D., Mali, V. P., Sudrik, S. G., and Sonawane, H. R., Media controlled photo-Favorskii type rearrangement of α-chloro acetophenones: synthesis of phenylacetic acids, Tetrahedron, 53, 16789-16794, 1997.
    • (1997) Tetrahedron , vol.53 , pp. 16789-16794
    • Dhavale, D.D.1    Mali, V.P.2    Sudrik, S.G.3    Sonawane, H.R.4
  • 34
    • 0028009112 scopus 로고
    • Photochemical rearrangement of α-chloropropiophenones to α-arylpropanoic acids: Studies on chirality transfer and synthesis of (S)-(+)-ibuprofen and (S)-(+)-ketoprofen
    • Sonawane, H. R., Bellur, N. S., Kulkarni, D. G., and Ayyangar, N. R., Photochemical rearrangement of α-chloropropiophenones to α-arylpropanoic acids: studies on chirality transfer and synthesis of (S)-(+)-ibuprofen and (S)-(+)-ketoprofen, Tetrahedron, 50, 1243-1260, 1994.
    • (1994) Tetrahedron , vol.50 , pp. 1243-1260
    • Sonawane, H.R.1    Bellur, N.S.2    Kulkarni, D.G.3    Ayyangar, N.R.4
  • 35
    • 0442283671 scopus 로고
    • A photo-induced rearrangement involving aryl participation
    • Anderson, J. C. and Reese, C. B., A photo-induced rearrangement involving aryl participation, Tetrahedron Lett., 1-4, 1962.
    • (1962) Tetrahedron Lett , pp. 1-4
    • Anderson, J.C.1    Reese, C.B.2
  • 36
    • 0030603031 scopus 로고    scopus 로고
    • Hydroxyphenacyl ATP: A new phototrigger
    • Givens, R. S. and Park, C.-H., Hydroxyphenacyl ATP: a new phototrigger, Tetrahedron Lett., 37, 6259-6262, 1996.
    • (1996) Tetrahedron Lett , vol.37 , pp. 6259-6262
    • Givens, R.S.1    Park, C.-H.2
  • 37
    • 0030907953 scopus 로고    scopus 로고
    • New photoactivated protecting groups. 6. p-Hydroxyphenacyl: A phototrigger for chemical and biochemical probes
    • Park, C.-H. and Givens, R. S., New photoactivated protecting groups. 6. p-Hydroxyphenacyl: a phototrigger for chemical and biochemical probes J. Am. Chem. Soc., 119, 2453-2463, 1997.
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 2453-2463
    • Park, C.-H.1    Givens, R.S.2
  • 38
    • 0033597621 scopus 로고    scopus 로고
    • Mechanism of photosolvolytic rearrangement of p-hydroxyphenacyl esters: Evidence for excited-state intramolecular proton transfer as the primary photochemical step
    • Zhang, K., Corrie, J. E. T., Munasinghe, R. N., and Wan, P., Mechanism of photosolvolytic rearrangement of p-hydroxyphenacyl esters: evidence for excited-state intramolecular proton transfer as the primary photochemical step, J. Am. Chem. Soc., 121, 5625-5632, 1999.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 5625-5632
    • Zhang, K.1    Corrie, J.E.T.2    Munasinghe, R.N.3    Wan, P.4
  • 39
    • 0032565121 scopus 로고    scopus 로고
    • m-Quinone methides from m-hydroxy-1,1-diaryl alkenes via excitedstate (formal)intramolecular proton transfer mediated by a witer timer
    • Fischer, M. and Wan, P., m-Quinone methides from m-hydroxy-1,1-diaryl alkenes via excitedstate (formal)intramolecular proton transfer mediated by a witer timer, J. Am. Chem. Soc., 120, 2680-2681, 1998.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 2680-2681
    • Fischer, M.1    Wan, P.2
  • 40
    • 0001550151 scopus 로고
    • Intramolecular proton transfer in photohydration reactions
    • Kalanderopoulos, P. and Yates, P., Intramolecular proton transfer in photohydration reactions, J. Am. Chem. Soc., 108, 6290-6295, 1986.
    • (1986) J. Am. Chem. Soc , vol.108 , pp. 6290-6295
    • Kalanderopoulos, P.1    Yates, P.2
  • 41
    • 0034721447 scopus 로고    scopus 로고
    • p-Hydroxyphenacyl phototriggers: The reactive excited state of phosphate photorelease
    • Conrad II, P. G., Givens, R. S., Hellrung, B., Rajesh, C. S., Ramseiir, M., and Wirz, J., p-Hydroxyphenacyl phototriggers: the reactive excited state of phosphate photorelease, J. Am. Chem. Soc., 122, 9346-9347, 2000.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 9346-9347
    • Conrad, P.G.1    Givens, R.S.2    Hellrung, B.3    Rajesh, C.S.4    Ramseiir, M.5    Wirz, J.6
  • 42
    • 0001334755 scopus 로고
    • Mechanistic organic photochemistry. II. Solvolytic photochemical reactions
    • Zimmerman, H. E. and Sandel, V. R., Mechanistic organic photochemistry. II. Solvolytic photochemical reactions, J. Am. Chem. Soc., 85, 915-922, 1963.
    • (1963) J. Am. Chem. Soc , vol.85 , pp. 915-922
    • Zimmerman, H.E.1    Sandel, V.R.2
  • 43
    • 0000810247 scopus 로고    scopus 로고
    • Meta-ortho effect in organic photochemistry: Mechanistic and exploratory organic photochemistry
    • Zimmerman, H. E., Meta-ortho effect in organic photochemistry: mechanistic and exploratory organic photochemistry, J. Phys. Chem. A, 102, 5616-5621, 1998.
    • (1998) J. Phys. Chem. A , vol.102 , pp. 5616-5621
    • Zimmerman, H.E.1
  • 44
    • 0000810247 scopus 로고    scopus 로고
    • Meta-ortho effect in organic photochemistry: Mechanistic and exploratory organic photochemistry
    • Erratum to document cited in CA129: 1353
    • Zimmerman, H. E., Meta-ortho effect in organic photochemistry: mechanistic and exploratory organic photochemistry. [Erratum to document cited in CA129: 1353] J. Phys. Chem. A, 102, 7725, 1998.
    • (1998) J. Phys. Chem. A , vol.102 , pp. 7725
    • Zimmerman, H.E.1
  • 45
    • 9444222661 scopus 로고
    • Photochemistry of substituted 1-naphthylmethyl esters of phenylacetic and 3-phenylpropanoic acid: Radical pairs, ion pairs and Marcus electron transfer
    • DeCosta, D. P. and Pincock, J. A., Photochemistry of substituted 1-naphthylmethyl esters of phenylacetic and 3-phenylpropanoic acid: radical pairs, ion pairs and Marcus electron transfer, J. Am. Chem. Soc., 115, 2180-2190, 1993.
    • (1993) J. Am. Chem. Soc , vol.115 , pp. 2180-2190
    • DeCosta, D.P.1    Pincock, J.A.2
  • 46
    • 0002447008 scopus 로고    scopus 로고
    • Photochemistry of arylmethyl esters in nucleophilic solvents: Radical pair and ion pair intermediates
    • Pincock, J. A., Photochemistry of arylmethyl esters in nucleophilic solvents: radical pair and ion pair intermediates, Acc. Chem. Res., 30, 43-49, 1997.
    • (1997) Acc. Chem. Res , vol.30 , pp. 43-49
    • Pincock, J.A.1
  • 47
    • 0030297164 scopus 로고    scopus 로고
    • Acyloxycoumarinylmethyl-caged cAMP: The photolabile and membrane-permeable derivative of cAMP that effectively stimulates pigment-dispersion response of melanophores
    • Furuta, T., Momotaka, A., Sugimoto, M., Hatayajma, M., Torigai, H., and Iwamura, M., Acyloxycoumarinylmethyl-caged cAMP: the photolabile and membrane-permeable derivative of cAMP that effectively stimulates pigment-dispersion response of melanophores, Biochem. Biophys. Res. Commun., 228, 193-198, 1996.
    • (1996) Biochem. Biophys. Res. Commun , vol.228 , pp. 193-198
    • Furuta, T.1    Momotaka, A.2    Sugimoto, M.3    Hatayajma, M.4    Torigai, H.5    Iwamura, M.6
  • 48
    • 0033537680 scopus 로고    scopus 로고
    • Synthesis and photochemistry of a photolabile precursor of N-methyl-D-aspartate (NMDA) that is photolyzed in the microsecond time region and is suitable for chemical kinetic investigations of the NMDA receptor
    • Gee, K. R., Niu, L., Schaper, K., Jayaraman, V., and Hess, G. P., Synthesis and photochemistry of a photolabile precursor of N-methyl-D-aspartate (NMDA) that is photolyzed in the microsecond time region and is suitable for chemical kinetic investigations of the NMDA receptor, Biochemistry, 38, 3140-3147, 1999.
    • (1999) Biochemistry , vol.38 , pp. 3140-3147
    • Gee, K.R.1    Niu, L.2    Schaper, K.3    Jayaraman, V.4    Hess, G.P.5
  • 49
    • 0029024496 scopus 로고
    • Synthesis of oligonucleotides containing 3'-alkyl carboxylic acids using universal, photolabile solid phase synthesis supports
    • Yoo, D. J. and Greenberg, M., Synthesis of oligonucleotides containing 3'-alkyl carboxylic acids using universal, photolabile solid phase synthesis supports, J. Org. Chem., 60, 3358-3364, 1995.
    • (1995) J. Org. Chem , vol.60 , pp. 3358-3364
    • Yoo, D.J.1    Greenberg, M.2
  • 50
    • 0032783950 scopus 로고    scopus 로고
    • 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
    • Schade, B., Hagen, V., Schmidt, R., Herbrich, R., Krause, E., Eckardt, T., and Bendig, J., 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., 64, 9109-9117, 1999.
    • (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
  • 51
    • 0034203977 scopus 로고    scopus 로고
    • New phototriggers: Extending the p-hydroxyphenacyl π-π* absorption range
    • Conrad II, P. G., Givens, R. S., Weber, J. F. W., and Kandler, K., New phototriggers: extending the p-hydroxyphenacyl π-π* absorption range, Org. Lett., 2, 1545-1547, 2000.
    • (2000) Org. Lett , vol.2 , pp. 1545-1547
    • Conrad, P.G.1    Givens, R.S.2    Weber, J.F.W.3    Kandler, K.4
  • 52
    • 0034728648 scopus 로고    scopus 로고
    • New phototriggers. 9. p-Cydroxyphenacyl as a C-terminal photoremovable protecting group for oligopeptides
    • Givens, R. S., Weber, J. F. W., Conrad II, P. G., Orosz, G., Donahue, S. L., and Thayer, S. A., New phototriggers. 9. p-Cydroxyphenacyl as a C-terminal photoremovable protecting group for oligopeptides, J. Am. Chem. Soc., 122, 2687-2697, 2000.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 2687-2697
    • Givens, R.S.1    Weber, J.F.W.2    Conrad, P.G.3    Orosz, G.4    Donahue, S.L.5    Thayer, S.A.6
  • 53
    • 0031575621 scopus 로고    scopus 로고
    • The use of a dithiane protected benzoin photolabile safety catch linker for solid-phase synthesis
    • Routledge, A., Abell, C., and Balasubramanian, S., The use of a dithiane protected benzoin photolabile safety catch linker for solid-phase synthesis, Tetrahedron Lett., 38, 1227-1230, 1997.
    • (1997) Tetrahedron Lett , vol.38 , pp. 1227-1230
    • Routledge, A.1    Abell, C.2    Balasubramanian, S.3
  • 54
    • 0442295210 scopus 로고    scopus 로고
    • 2,5-Dimethylphenacyl as a new photoreleasable-protecting group for carboxylic acids
    • Klan, P., Zabadal, M., and Heger, D., 2,5-Dimethylphenacyl as a new photoreleasable-protecting group for carboxylic acids, Org. Lett., 2, 1569-1571, 2000.
    • (2000) Org. Lett , vol.2 , pp. 1569-1571
    • Klan, P.1    Zabadal, M.2    Heger, D.3
  • 55
    • 0035892201 scopus 로고    scopus 로고
    • 2,5-Dimethylphenacyl esters: A photoremovable protecting group for carboxylic acids
    • Zabadal, M., Pelliccioli, A. P., Klan, P., and Wirz, J., 2,5-Dimethylphenacyl esters: a photoremovable protecting group for carboxylic acids, J. Phys. Chem. A, 105, 10329-10333, 2001.
    • (2001) J. Phys. Chem. A , vol.105 , pp. 10329-10333
    • Zabadal, M.1    Pelliccioli, A.P.2    Klan, P.3    Wirz, J.4
  • 56
    • 0001368167 scopus 로고    scopus 로고
    • Orthogonal photolysis of protecting groups
    • Bochet, C. G., Orthogonal photolysis of protecting groups, Angew. Chem., Int. Ed. Engl., 40, 2071-2073, 2001.
    • (2001) Angew. Chem., Int. Ed. Engl , vol.40 , pp. 2071-2073
    • Bochet, C.G.1
  • 57
    • 33845279305 scopus 로고
    • Photolabile 1-(2-nitrophenyl)ethyl phosphate esters of adenine nucleotide analogues: Synthesis and mechanism of photolysis
    • Walker, J. W., Reid, G. P., McCray, J. A., and Trentham, D. R., Photolabile 1-(2-nitrophenyl)ethyl phosphate esters of adenine nucleotide analogues: synthesis and mechanism of photolysis, J. Am. Chem. Soc., 110, 7170-7177, 1988.
    • (1988) J. Am. Chem. Soc , vol.110 , pp. 7170-7177
    • Walker, J.W.1    Reid, G.P.2    McCray, J.A.3    Trentham, D.R.4
  • 58
    • 33751155704 scopus 로고
    • Photochemical properties of new photolabile cAMP derivatives in a physiological saline solution
    • Furuta, T., Torigai, M., Sugimoto, M., and Iwamura, M., Photochemical properties of new photolabile cAMP derivatives in a physiological saline solution, J. Org. Chem., 60, 3953-3956, 1995.
    • (1995) J. Org. Chem , vol.60 , pp. 3953-3956
    • Furuta, T.1    Torigai, M.2    Sugimoto, M.3    Iwamura, M.4
  • 59
    • 0031799503 scopus 로고    scopus 로고
    • New caged groups: 7-substituted coumarinylmethyl phosphate esters
    • Marriott, G., Ed., Academic Press, New York
    • Furuta, T. and Iwamura, M., New caged groups: 7-substituted coumarinylmethyl phosphate esters, in Methods in Enzymology, Vol. 291, Marriott, G., Ed., Academic Press, New York, 1998, 50-63.
    • (1998) Methods in Enzymology , vol.291 , pp. 50-63
    • Furuta, T.1    Iwamura, M.2
  • 60
    • 0035857544 scopus 로고    scopus 로고
    • Highly efficient and ultrafast phototriggers for cAMP and cGMP by using long-wavelength UV/VIS activation, Angew. Chem
    • Hagen, V., Bendig, J., Frings, S., Eckardt, T., Helm, S., Reuter, D., and Kaupp, U. B., Highly efficient and ultrafast phototriggers for cAMP and cGMP by using long-wavelength UV/VIS activation, Angew. Chem., Int. Ed. Engl., 40, 1046-1048, 2001.
    • (2001) Int. Ed. Engl , vol.40 , pp. 1046-1048
    • Hagen, V.1    Bendig, J.2    Frings, S.3    Eckardt, T.4    Helm, S.5    Reuter, D.6    Kaupp, U.B.7
  • 61
    • 0034708735 scopus 로고    scopus 로고
    • The mechanism of GTP hydrolysis by Ras probed by Fourier transform infrared spectroscopy
    • Du, X., Frei, H., and Kim, S.-H., The mechanism of GTP hydrolysis by Ras probed by Fourier transform infrared spectroscopy, J. Biol. Chem., 275, 8492-8500, 2000.
    • (2000) J. Biol. Chem , vol.275 , pp. 8492-8500
    • Du, X.1    Frei, H.2    Kim, S.-H.3
  • 63
    • 33751158037 scopus 로고
    • Photoremovable-protecting groups for phosphorylation of chiral alcohols: Asymmetric synthesis of phosphotriesters of (-)-3',5'-dimethoxybenzoin
    • Pirrung, M. C. and Shuey, S. W., Photoremovable-protecting groups for phosphorylation of chiral alcohols: asymmetric synthesis of phosphotriesters of (-)-3',5'-dimethoxybenzoin, J. Org. Chem., 59, 3890-3897, 1994.
    • (1994) J. Org. Chem , vol.59 , pp. 3890-3897
    • Pirrung, M.C.1    Shuey, S.W.2
  • 64
    • 0035945765 scopus 로고    scopus 로고
    • Reductive ring opening of o-nitrobenzylidene acetals of monosaccharides: Synthesis and photolysis of some photolabile sugars
    • Watanabe, S., Sueyoshi, T., Ichihara, M., Uehara, C., and Iwamura, M., Reductive ring opening of o-nitrobenzylidene acetals of monosaccharides: synthesis and photolysis of some photolabile sugars, Org. Lett., 3, 255-257, 2001.
    • (2001) Org. Lett , vol.3 , pp. 255-257
    • Watanabe, S.1    Sueyoshi, T.2    Ichihara, M.3    Uehara, C.4    Iwamura, M.5
  • 65
    • 0037078809 scopus 로고    scopus 로고
    • Peptide-small molecule hybrids via orthogonal deprotection-chemoselective conjugation to cysteine-anchored scaffolds: A model study
    • Smith, A. B., Savinov, S. N., Manjappara, U. V., and Chaiken, I. M., Peptide-small molecule hybrids via orthogonal deprotection-chemoselective conjugation to cysteine-anchored scaffolds: a model study, Org. Lett., 4, 4041-4044, 2002.
    • (2002) Org. Lett , vol.4 , pp. 4041-4044
    • Smith, A.B.1    Savinov, S.N.2    Manjappara, U.V.3    Chaiken, I.M.4
  • 67
    • 0031760872 scopus 로고    scopus 로고
    • New photolabile protecting groups in nucleoside and nucleotide chemistry: Synthesis, cleavage mechanisms and applications
    • Giegrich, H., Eisele-Buhler, S., Hermann, C., Kvasyuk, E., Charubala, R., and Pfleiderer, W., New photolabile protecting groups in nucleoside and nucleotide chemistry: synthesis, cleavage mechanisms and applications, Nucleosides Nucleotides, 17, 1987-1996, 1998.
    • (1998) Nucleosides Nucleotides , vol.17 , pp. 1987-1996
    • Giegrich, H.1    Eisele-Buhler, S.2    Hermann, C.3    Kvasyuk, E.4    Charubala, R.5    Pfleiderer, W.6
  • 68
    • 0034895535 scopus 로고    scopus 로고
    • Photolabile protecting groups for nucleosides: Mechanistic studies of the 2-(2-nitrophenyl)ethyl group
    • Walbert, S., Pfleiderer, W., and Steiner, U. E., Photolabile protecting groups for nucleosides: mechanistic studies of the 2-(2-nitrophenyl)ethyl group, Helv. Chim. Acta, 84, 1601-1611, 2001.
    • (2001) Helv. Chim. Acta , vol.84 , pp. 1601-1611
    • Walbert, S.1    Pfleiderer, W.2    Steiner, U.E.3
  • 69
    • 0035912337 scopus 로고    scopus 로고
    • 3'-Nitrophenylpropyloxycarbonyl (NPPOC) protecting groups for high-fidelity automated 5' →3' photochemical DNA synthesis
    • Pirrung, M. C., Wang, L., and Montague-Smith, M. P., 3'-Nitrophenylpropyloxycarbonyl (NPPOC) protecting groups for high-fidelity automated 5' →3' photochemical DNA synthesis, Org. Lett., 3, 1105-1108, 2001.
    • (2001) Org. Lett , vol.3 , pp. 1105-1108
    • Pirrung, M.C.1    Wang, L.2    Montague-Smith, M.P.3
  • 70
    • 0033527766 scopus 로고    scopus 로고
    • The S-pixyl group: An efficient photocleavable-protecting group for the 5' hydroxy function of deoxyribonucleosides
    • Coleman, M. P. and Boyd, M. K., The S-pixyl group: an efficient photocleavable-protecting group for the 5' hydroxy function of deoxyribonucleosides, Tetrahedron Lett., 40, 7911-7915, 1999.
    • (1999) Tetrahedron Lett , vol.40 , pp. 7911-7915
    • Coleman, M.P.1    Boyd, M.K.2
  • 71
    • 0037134202 scopus 로고    scopus 로고
    • A strategy for the construction of caged diols using a photolabile protecting group
    • Lin, W. and Lawrence, D. S., A strategy for the construction of caged diols using a photolabile protecting group, J. Org. Chem., 67, 2723-2726, 2002.
    • (2002) J. Org. Chem , vol.67 , pp. 2723-2726
    • Lin, W.1    Lawrence, D.S.2
  • 72
    • 85056360573 scopus 로고    scopus 로고
    • Intermolecular ion pairs have been observed in the photolysis of caged methoxycoumarin derivatives; see Reference 46
    • Intermolecular ion pairs have been observed in the photolysis of caged methoxycoumarin derivatives; see Reference 46.
  • 73
    • 0001374343 scopus 로고
    • Dimethoxybenzoin carbonates: Photochemically removable alcohol protecting groups suitable for phosphoramidite-based DNA synthesis
    • Pirrung, M. C. and Bradley, J.-C., Dimethoxybenzoin carbonates: photochemically removable alcohol protecting groups suitable for phosphoramidite-based DNA synthesis, J. Org. Chem., 60, 1116-1117, 1995.
    • (1995) J. Org. Chem , vol.60 , pp. 1116-1117
    • Pirrung, M.C.1    Bradley, J.-C.2
  • 74
    • 0000624247 scopus 로고    scopus 로고
    • Anthraquinon-2-ylmethoxycarbonyl (Aqmoc): A new photochemically removable-protecting group for alcohols
    • Furuta, T., Hirayama, Y., and Iwamura, M., Anthraquinon-2-ylmethoxycarbonyl (Aqmoc): a new photochemically removable-protecting group for alcohols, Org. Lett., 3, 1809-1812, 2001.
    • (2001) Org. Lett , vol.3 , pp. 1809-1812
    • Furuta, T.1    Hirayama, Y.2    Iwamura, M.3
  • 75
    • 0035813448 scopus 로고    scopus 로고
    • N-methyl-N-(o-nitrophenyl)carbamates as photolabile alcohol protecting groups
    • Loudwig, S. and Goeldner, M., N-methyl-N-(o-nitrophenyl)carbamates as photolabile alcohol protecting groups, Tetrahedron Lett., 42, 7957-7959, 2001.
    • (2001) Tetrahedron Lett , vol.42 , pp. 7957-7959
    • Loudwig, S.1    Goeldner, M.2
  • 76
    • 85056345824 scopus 로고    scopus 로고
    • The carbamate cage is inert to strong non-nucleophilic bases such as LDA
    • The carbamate cage is inert to strong non-nucleophilic bases such as LDA.
  • 77
    • 0034829409 scopus 로고    scopus 로고
    • Photochemically removable silyl protecting groups
    • Pirrung, M. C., Fallon, L., Zhu, J., and Lee, Y. R. Photochemically removable silyl protecting groups, J. Am. Chem. Soc., 123, 3638-3643, 2001.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 3638-3643
    • Pirrung, M.C.1    Fallon, L.2    Zhu, J.3    Lee, Y.R.4
  • 78
    • 0000999179 scopus 로고
    • Photochemically removable silyl protecting groups
    • Pirrung, M. C. and Lee, Y. R., Photochemically removable silyl protecting groups, J. Org. Chem., 58, 6961-6963, 1993.
    • (1993) J. Org. Chem , vol.58 , pp. 6961-6963
    • Pirrung, M.C.1    Lee, Y.R.2
  • 80
    • 0000310486 scopus 로고    scopus 로고
    • 2-Benzoylbenzoic acid: A photolabile mask for alcohols and thiols
    • Jones, P. B., Pollastri, M. P., and Porter, N. A., 2-Benzoylbenzoic acid: a photolabile mask for alcohols and thiols, J. Org. Chem., 61, 9455-9461, 1996.
    • (1996) J. Org. Chem , vol.61 , pp. 9455-9461
    • Jones, P.B.1    Pollastri, M.P.2    Porter, N.A.3
  • 81
    • 0002702431 scopus 로고
    • Photoreduction of aromatic ketones by amines: Studies of quantum yields and mechanism
    • Based on the photoreduction mechanism proposed for benzophenone in the presence of amines
    • Based on the photoreduction mechanism proposed for benzophenone in the presence of amines, Cohen, S. G. and Chao, H. M., Photoreduction of aromatic ketones by amines: studies of quantum yields and mechanism, J. Am. Chem. Soc., 90, 165-173, 1968.
    • (1968) J. Am. Chem. Soc , vol.90 , pp. 165-173
    • Cohen, S.G.1    Chao, H.M.2
  • 85
    • 0035925126 scopus 로고    scopus 로고
    • Competitive photochemical reactivity in a self-assembled monolayer on a colloidal gold cluster
    • Hu, J., Zhang, J., Liu, F., Kittredge, K., Whitesell, J. K., and Fox, M. A., Competitive photochemical reactivity in a self-assembled monolayer on a colloidal gold cluster, J. Am. Chem. Soc., 123, 1464-1470, 2001.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 1464-1470
    • Hu, J.1    Zhang, J.2    Liu, F.3    Kittredge, K.4    Whitesell, J.K.5    Fox, M.A.6
  • 86
    • 17344372573 scopus 로고    scopus 로고
    • Design, synthesis and photochemical properties of a photoreleasable ubiquinol-2: A novel compound for studying rapid electron-transfer kinetics in ubiquinol-oxidizing enzymes
    • Stowell, M. H. B., Wang, G., Day, M. W., and Chan, S. I., Design, synthesis and photochemical properties of a photoreleasable ubiquinol-2: a novel compound for studying rapid electron-transfer kinetics in ubiquinol-oxidizing enzymes, J. Am. Chem. Soc., 120, 1657-1664, 1998.
    • (1998) J. Am. Chem. Soc , vol.120 , pp. 1657-1664
    • Stowell, M.H.B.1    Wang, G.2    Day, M.W.3    Chan, S.I.4
  • 87
    • 1542545396 scopus 로고
    • Photogeneration of organic bases from o-nitrobenzyl derived carbamates
    • Cameron, J. F. and Frechet, J. M. J., Photogeneration of organic bases from o-nitrobenzyl derived carbamates, J. Am. Chem. Soc., 113, 4303-4313, 1991.
    • (1991) J. Am. Chem. Soc , vol.113 , pp. 4303-4313
    • Cameron, J.F.1    Frechet, J.M.J.2
  • 88
    • 0029089532 scopus 로고
    • Photochemical deprotection of 3',5'-dimethoxybenzoin (DMB) carbamates derived from secondary amines
    • Pirrung, M. C. and Huang, C.-Y., Photochemical deprotection of 3',5'-dimethoxybenzoin (DMB) carbamates derived from secondary amines, Tetrahedron Lett., 36, 5883-5884, 1995.
    • (1995) Tetrahedron Lett , vol.36 , pp. 5883-5884
    • Pirrung, M.C.1    Huang, C.-Y.2
  • 89
    • 33748597950 scopus 로고    scopus 로고
    • Synthesis and evaluation of photolabile sulfonamides as potential reagents for rapid photorelease of neuroactive amines
    • Corrie, J. E. T. and Papageorgiou, G., Synthesis and evaluation of photolabile sulfonamides as potential reagents for rapid photorelease of neuroactive amines, J. Chem. Soc., Perkin Trans. 1, 1583-1591, 1996.
    • (1996) J. Chem. Soc., Perkin Trans , vol.1 , pp. 1583-1591
    • Corrie, J.E.T.1    Papageorgiou, G.2
  • 90
    • 0000472668 scopus 로고
    • Selective removal of electron-accepting p-toluene and naphthalenesulfonyl protecting groups for amino function via photoinduced donor-acceptor ion pairs with electron donating aromatics
    • Hamada, T., Nishida, A., and Yonemitsu, O., Selective removal of electron-accepting p-toluene and naphthalenesulfonyl protecting groups for amino function via photoinduced donor-acceptor ion pairs with electron donating aromatics, J. Am. Chem. Soc., 108, 140-145, 1986.
    • (1986) J. Am. Chem. Soc , vol.108 , pp. 140-145
    • Hamada, T.1    Nishida, A.2    Yonemitsu, O.3
  • 91
    • 0013511213 scopus 로고
    • A new amino protecting group readily removable with near ultraviolet light as an application of electron-transfer photochemistry
    • Hamada, T., Nishida, A., and Yonemitsu, O., A new amino protecting group readily removable with near ultraviolet light as an application of electron-transfer photochemistry, Tetrahedron Lett., 30, 4241-4244, 1989.
    • (1989) Tetrahedron Lett , vol.30 , pp. 4241-4244
    • Hamada, T.1    Nishida, A.2    Yonemitsu, O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.