메뉴 건너뛰기




Volumn , Issue , 2008, Pages 249-276

5-Substituted Nucleosides in Biochemistry and Biotechnology

Author keywords

5 substituted nucleosides; DNA duplexes; Organopalladium coupling; Photochemistry; T7 RNA polymerase

Indexed keywords


EID: 84889384894     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527623112.ch10     Document Type: Chapter
Times cited : (12)

References (90)
  • 1
    • 0037944068 scopus 로고    scopus 로고
    • Palladium-assisted routes to nucleosides
    • Agrofoglio, L. A., Gillaizeau, I., et al. Palladium-assisted routes to nucleosides. Chem. Rev. 2003, 103 (5), 1875-1916.
    • (2003) , vol.103 , Issue.5 , pp. 1875-1916
    • Agrofoglio, L.A.1    Gillaizeau, I.2
  • 2
    • 0042009118 scopus 로고    scopus 로고
    • Efficient one-step Suzuki arylation of unprotected halonucleosides, using water-soluble palladium catalysts
    • Western, E. C., Daft, J. R., et al. Efficient one-step Suzuki arylation of unprotected halonucleosides, using water-soluble palladium catalysts. J. Org. Chem. 2003, 68 (17), 6767-6774.
    • (2003) J. Org. Chem. , vol.68 , Issue.17 , pp. 6767-6774
    • Western, E.C.1    Daft, J.R.2
  • 3
    • 0344413525 scopus 로고    scopus 로고
    • Microwaveenhanced Sonogashira coupling reaction of substituted pyrimidinones and pyrimidine nucleosides
    • Petricci, E., Radi, M., et al. Microwaveenhanced Sonogashira coupling reaction of substituted pyrimidinones and pyrimidine nucleosides. Tetrahedron Lett. 2003, 44 (51), 9181-9184.
    • (2003) Tetrahedron Lett. , vol.44 , Issue.51 , pp. 9181-9184
    • Petricci, E.1    Radi, M.2
  • 4
    • 4944247395 scopus 로고    scopus 로고
    • Palladium-catalyzed synthesis of uridines on polystyrene-based solid supports
    • Aucagne, V., Berteina-Raboin, S., et al. Palladium-catalyzed synthesis of uridines on polystyrene-based solid supports. J. CombinatorialChem. 2004, 6 (5), 717-723.
    • (2004) J. CombinatorialChem. , vol.6 , Issue.5 , pp. 717-723
    • Aucagne, V.1    Berteina-Raboin, S.2
  • 5
    • 0141869063 scopus 로고    scopus 로고
    • A versatile modification of on-column oligodeoxynucleotides using a coppercatalyzed oxidative acetylenic coupling reaction
    • Minakawa, N., Ono, Y., et al. A versatile modification of on-column oligodeoxynucleotides using a coppercatalyzed oxidative acetylenic coupling reaction. J. Am. Chem. Soc. 2003, 125 (38), 11545-11552.
    • (2003) J. Am. Chem. Soc. , vol.125 , Issue.38 , pp. 11545-11552
    • Minakawa, N.1    Ono, Y.2
  • 6
    • 0028226446 scopus 로고
    • Nucleosides and nucleotid. 127. A novel and convenient post-synthetic modification method for the synthesis of oligodeoxyribonucleotides carrying amino linkers at the 5-position of 20-deoxyuridine
    • Ono, A., Haginoya, N., et al. Nucleosides and nucleotid. 127. A novel and convenient post-synthetic modification method for the synthesis of oligodeoxyribonucleotides carrying amino linkers at the 5-position of 20-deoxyuridine. Bioorg. Medicinal Chem. Lett. 1994, 4 (2), 361-366.
    • (1994) Bioorg. Medicinal Chem. Lett. , vol.4 , Issue.2 , pp. 361-366
    • Ono, A.1    Haginoya, N.2
  • 7
    • 0031148944 scopus 로고    scopus 로고
    • Nucleosides and nucleotide. 160. Synthesis of oligodeoxyribonucleotides containing 5-(N-aminoalkyl)carbamoyl-20-deoxyuridine by a new postsynthetic modification method and their thermal stability and nuclease-resistance properties
    • Haginoya, N., Ono, A., et al. Nucleosides and nucleotide. 160. Synthesis of oligodeoxyribonucleotides containing 5-(N-aminoalkyl)carbamoyl-20-deoxyuridine by a new postsynthetic modification method and their thermal stability and nuclease-resistance properties. Bioconj. Chem. 1997, 8 (3), 271-280.
    • (1997) Bioconj. Chem. , vol.8 , Issue.3 , pp. 271-280
    • Haginoya, N.1    Ono, A.2
  • 8
    • 0344494605 scopus 로고    scopus 로고
    • Synthesis of oligonucleotides modified with polyamines and their properties as antisense and antigene molecules
    • Ueno, Y. and Matsuda, A. Synthesis of oligonucleotides modified with polyamines and their properties as antisense and antigene molecules. J. Synthetic Org. Chem. Japan 2003, 61 (9), 890-899.
    • (2003) J. Synthetic Org. Chem. Japan , vol.61 , Issue.9 , pp. 890-899
    • Ueno, Y.1    Matsuda, A.2
  • 9
    • 0032482513 scopus 로고    scopus 로고
    • Synthesis of a novel 20-deoxyuridine derivative bearing a cyanomethoxy-carbonylmethyl group at C-5 position and its use for versatile post-synthetic functionalization of oligodeoxyribonucleotides
    • Kohgo, S., Shinozuka, K., et al. Synthesis of a novel 20-deoxyuridine derivative bearing a cyanomethoxy-carbonylmethyl group at C-5 position and its use for versatile post-synthetic functionalization of oligodeoxyribonucleotides. Tetrahedron Lett. 1998, 39 (23), 4067-4070.
    • (1998) Tetrahedron Lett. , vol.39 , Issue.23 , pp. 4067-4070
    • Kohgo, S.1    Shinozuka, K.2
  • 10
    • 0034614564 scopus 로고    scopus 로고
    • Multifunctionalization of oligodeoxynucleotide: a facile post-synthetic modification technique for the preparation of oligodeoxynucleotides with two different functional molecules
    • Shinozuka, K., Kohgo, S., et al. Multifunctionalization of oligodeoxynucleotide: a facile post-synthetic modification technique for the preparation of oligodeoxynucleotides with two different functional molecules. Chem. Commun. 2000, 59-60.
    • (2000) , pp. 59-60
    • Shinozuka, K.1    Kohgo, S.2
  • 11
    • 4444234581 scopus 로고    scopus 로고
    • Stabilizing or destabilizing oligodeoxynucleotide duplexes containing single 20-deoxyuridine residues with 5-alkynyl substituents
    • Kottysch, T., Ahlborn, C., et al. Stabilizing or destabilizing oligodeoxynucleotide duplexes containing single 20-deoxyuridine residues with 5-alkynyl substituents. Chemistry-A European Journal 2004, 10 (16), 4017-4028.
    • (2004) Chemistry-A European Journal , vol.10 , Issue.16 , pp. 4017-4028
    • Kottysch, T.1    Ahlborn, C.2
  • 12
    • 32144445388 scopus 로고    scopus 로고
    • Synthesis of oligonucleotides with 30-terminal 5-(3-acylamidopropargyl)-30-amino-20,30-dideoxyuridine residues and their reactivity in single-nucleotide steps of chemical replication
    • Baumhof, P., Griesang, N., et al. Synthesis of oligonucleotides with 30-terminal 5-(3-acylamidopropargyl)-30-amino-20,30-dideoxyuridine residues and their reactivity in single-nucleotide steps of chemical replication. J. Org. Chem. 2006, 71 (3), 1060-1067.
    • (2006) J. Org. Chem. , vol.71 , Issue.3 , pp. 1060-1067
    • Baumhof, P.1    Griesang, N.2
  • 13
    • 0035856963 scopus 로고    scopus 로고
    • Ketone-DNA: A versatile postsynthetic DNA decoration platform
    • Dey, S. and Sheppard, T. L. Ketone-DNA: A versatile postsynthetic DNA decoration platform. Org. Lett. 2001, 3 (25), 3983-3986.
    • (2001) Org. Lett. , vol.3 , Issue.25 , pp. 3983-3986
    • Dey, S.1    Sheppard, T.L.2
  • 14
    • 33748609388 scopus 로고    scopus 로고
    • Click chemistry as a reliable method for the high-density postsynthetic functionalization of alkyne-modified DNA
    • Gierlich, J., Burley, G. A., et al. Click chemistry as a reliable method for the high-density postsynthetic functionalization of alkyne-modified DNA. Org. Lett. 2006, 8 (17), 3639-3642.
    • (2006) Org. Lett. , vol.8 , Issue.17 , pp. 3639-3642
    • Gierlich, J.1    Burley, G.A.2
  • 15
    • 14744297399 scopus 로고    scopus 로고
    • A cysteineappended deoxyuridine for the postsynthetic DNA modification using native chemical ligation
    • Takeda, S., Tsukiji, S., et al. A cysteineappended deoxyuridine for the postsynthetic DNA modification using native chemical ligation. Tetrahedron Lett. 2005, 46 (13), 2235-2238.
    • (2005) Tetrahedron Lett. , vol.46 , Issue.13 , pp. 2235-2238
    • Takeda, S.1    Tsukiji, S.2
  • 16
    • 0036644276 scopus 로고    scopus 로고
    • Internal labeling of oligonucleotide probes by Diels-Alder cycloaddition
    • Graham, D., Grondin, A., et al. Internal labeling of oligonucleotide probes by Diels-Alder cycloaddition. Tetrahedron Lett. 2002, 43 (27), 4785-4788.
    • (2002) Tetrahedron Lett. , vol.43 , Issue.27 , pp. 4785-4788
    • Graham, D.1    Grondin, A.2
  • 17
    • 0033518570 scopus 로고    scopus 로고
    • Introducing structural diversity in oligonucleotides via photolabile, convertible C5-substituted nucleotides
    • Kahl, J. D. and Greenberg, M. M. Introducing structural diversity in oligonucleotides via photolabile, convertible C5-substituted nucleotides. J.Am. Chem. Soc. 1999, 121 (4), 597-604.
    • (1999) J.Am. Chem. Soc. , vol.121 , Issue.4 , pp. 597-604
    • Kahl, J.D.1    Greenberg, M.M.2
  • 18
    • 0001001012 scopus 로고
    • Synthesis and enzymatic polymerization of nucleotides containing mercury: potential tools for nucleicacid sequencing and structuralanalysis
    • Dale, R. M. K., Livingston, D. C., Ward, D. C., and Martin, E. Synthesis and enzymatic polymerization of nucleotides containing mercury: potential tools for nucleicacid sequencing and structuralanalysis. Proc. Natl. Acad. Sci. USA 1973, 70 (8), 2238-2242.
    • (1973) Proc. Natl. Acad. Sci. USA , vol.70 , Issue.8 , pp. 2238-2242
    • Dale, R.M.K.1    Livingston, D.C.2    Ward, D.C.3    Martin, E.4
  • 19
    • 0016836165 scopus 로고
    • Mercurated polynucleotides-new probes for hybridization and selective polymer fractionation
    • Dale, R. M. K. and Ward, D. C. Mercurated polynucleotides-new probes for hybridization and selective polymer fractionation. Biochemistry 1975, 14 (11), 2458-2469.
    • (1975) Biochemistry , vol.14 , Issue.11 , pp. 2458-2469
    • Dale, R.M.K.1    Ward, D.C.2
  • 20
    • 0016734532 scopus 로고
    • Direct covalent mercuration of nucleotides and polynucleotides
    • Dale, R. M. K., Martin, E., et al. Direct covalent mercuration of nucleotides and polynucleotides. Biochemistry 1975, 14 (11), 2447-2457.
    • (1975) Biochemistry , vol.14 , Issue.11 , pp. 2447-2457
    • Dale, R.M.K.1    Martin, E.2
  • 21
    • 0023057515 scopus 로고
    • A nonradioactive in situ hybridization method based on mercurated nucleic-acid probes and sulfhydryl-hapten ligands
    • Hopman, A. H. N., Wiegant, J., et al. A nonradioactive in situ hybridization method based on mercurated nucleic-acid probes and sulfhydryl-hapten ligands. Nucleic Acids Res. 1986, 14 (16), 6471-6488.
    • (1986) Nucleic Acids Res. , vol.14 , Issue.16 , pp. 6471-6488
    • Hopman, A.H.N.1    Wiegant, J.2
  • 22
    • 0022655072 scopus 로고
    • A new hybridocytochemical method based on mercurated nucleic-acid probes and sulfhydryl-hapten ligands. 1. Stability of the mercury-sulfhydryl bond and influence of the ligand structure on immunochemical detection of the hapten
    • Hopman, A. H. N., Wiegant, J., et al. A new hybridocytochemical method based on mercurated nucleic-acid probes and sulfhydryl-hapten ligands. 1. Stability of the mercury-sulfhydryl bond and influence of the ligand structure on immunochemical detection of the hapten. Histochemistry 1986, 84 (2), 169-178.
    • (1986) Histochemistry , vol.84 , Issue.2 , pp. 169-178
    • Hopman, A.H.N.1    Wiegant, J.2
  • 23
    • 0022647785 scopus 로고
    • A new hybridocytochemical method based on mercurated nucleicacid probes and sulfhydryl-hapten ligands. 2. Effects of variations in ligand structure on the in situ detection of mercurated probes
    • Hopman, A. H. N., Wiegant, J., et al. A new hybridocytochemical method based on mercurated nucleicacid probes and sulfhydryl-hapten ligands. 2. Effects of variations in ligand structure on the in situ detection of mercurated probes. Histochemistry 1986, 84 (2), 179-185.
    • (1986) Histochemistry , vol.84 , Issue.2 , pp. 179-185
    • Hopman, A.H.N.1    Wiegant, J.2
  • 24
    • 0023121015 scopus 로고
    • Mercurated nucleicacid probes, a new principle for nonradioactive in situ hybridization
    • Hopman, A. H. N., Wiegant, J., et al. Mercurated nucleicacid probes, a new principle for nonradioactive in situ hybridization. Exp. Cell Res. 1987, 169 (2), 357-368.
    • (1987) Exp. Cell Res. , vol.169 , Issue.2 , pp. 357-368
    • Hopman, A.H.N.1    Wiegant, J.2
  • 25
    • 0000477103 scopus 로고
    • Enzymatic-synthesis of biotin-labeled polynucleotides-novel nucleicacid affinity probes
    • Langer, P. R., Waldrop, A. A., et al. Enzymatic-synthesis of biotin-labeled polynucleotides-novel nucleicacid affinity probes. Proc. Natl. Acad. Sci. USA-Biol. Sci. 1981, 78 (11), 6633-6637.
    • (1981) Proc. Natl. Acad. Sci. USA-Biol. Sci. , vol.78 , Issue.11 , pp. 6633-6637
    • Langer, P.R.1    Waldrop, A.A.2
  • 26
    • 0017309482 scopus 로고
    • Synthesis of C-5 substituted pyrimidine nucleosides via organo-palladium intermediates
    • Bergstrom, D. E. and Ruth, J. L. Synthesis of C-5 substituted pyrimidine nucleosides via organo-palladium intermediates. J. Am. Chem. Soc. 1976, 98 (6), 1587-1589.
    • (1976) J. Am. Chem. Soc. , vol.98 , Issue.6 , pp. 1587-1589
    • Bergstrom, D.E.1    Ruth, J.L.2
  • 27
    • 0000229241 scopus 로고
    • C-5 Substituted pyrimidine nucleosides. 2. Synthesis via olefin coupling to organopalladium intermediates derived from uridine and 20-deoxyuridine
    • Bergstrom, D. E. and Ogawa,. K. C-5 Substituted pyrimidine nucleosides. 2. Synthesis via olefin coupling to organopalladium intermediates derived from uridine and 20-deoxyuridine. J. Am. Chem. Soc. 1978, 100 (26), 8106-8112.
    • (1978) J. Am. Chem. Soc. , vol.100 , Issue.26 , pp. 8106-8112
    • Bergstrom, D.E.1    Ogawa, K.2
  • 28
    • 0017395826 scopus 로고
    • Modified polynucleotide. 1. Investigation of enzymatic polymerization of 5-alkyl-dUTP-s
    • Sagi, J. T., Szabolcs, A., et al. Modified polynucleotide. 1. Investigation of enzymatic polymerization of 5-alkyl-dUTP-s. Nucleic Acids Res. 1977, 4 (8), 2767-2777.
    • (1977) Nucleic Acids Res. , vol.4 , Issue.8 , pp. 2767-2777
    • Sagi, J.T.1    Szabolcs, A.2
  • 29
    • 0019334899 scopus 로고
    • Study of substratespecificity of mammalian and bacterial-DNA polymerases with 5-alkyl-20-deoxyuridine 50-triphosphates
    • Sagi, J., Nowak, R., et al. Study of substratespecificity of mammalian and bacterial-DNA polymerases with 5-alkyl-20-deoxyuridine 50-triphosphates. Biochim. Biophys. Acta 1980, 606 (2), 196-201.
    • (1980) Biochim. Biophys. Acta , vol.606 , Issue.2 , pp. 196-201
    • Sagi, J.1    Nowak, R.2
  • 30
    • 0019381631 scopus 로고
    • Nucleicacidrelated compounds. 31. Smooth and efficient palladium-copper catalyzed coupling of terminal alkynes with 5-iodouracil nucleosides
    • Robins, M. J. and Barr,. J. Nucleicacidrelated compounds. 31. Smooth and efficient palladium-copper catalyzed coupling of terminal alkynes with 5-iodouracil nucleosides. Tetrahedron Lett. 1981, 22 (5), 421-424.
    • (1981) Tetrahedron Lett. , vol.22 , Issue.5 , pp. 421-424
    • Robins, M.J.1    Barr, J.2
  • 31
    • 0032476840 scopus 로고    scopus 로고
    • Expanding the potential of DNA for binding and catalysis: highly functionalized dUTP derivatives that are substrates for thermostable DNA polymerases
    • Sakthivel, K. and Barbas, C. F. Expanding the potential of DNA for binding and catalysis: highly functionalized dUTP derivatives that are substrates for thermostable DNA polymerases. Angew. Chem.-Int. Ed. 1998, 37 (20), 2872-2875.
    • (1998) Angew. Chem.-Int. Ed. , vol.37 , Issue.20 , pp. 2872-2875
    • Sakthivel, K.1    Barbas, C.F.2
  • 32
    • 0036713391 scopus 로고    scopus 로고
    • Challenging artificial genetic systems: thymidine analogs with 5-position sulfur functionality
    • Held, H. A. and Benner, . A. Challenging artificial genetic systems: thymidine analogs with 5-position sulfur functionality. Nucleic Acids Res. 2002, 30 (17), 3857-3869.
    • (2002) Nucleic Acids Res. , vol.30 , Issue.17 , pp. 3857-3869
    • Held, H.A.1    Benner, A.2
  • 33
    • 1342332935 scopus 로고    scopus 로고
    • 20-Deoxycytidines carrying amino and thiol functionality: synthesis and incorporation by vent (exo(-)) polymerase
    • Roychowdhury, A., Illangkoon, H., et al. 20-Deoxycytidines carrying amino and thiol functionality: synthesis and incorporation by vent (exo(-)) polymerase. Org. Lett. 2004, 6 (4), 489-492.
    • (2004) Org. Lett. , vol.6 , Issue.4 , pp. 489-492
    • Roychowdhury, A.1    Illangkoon, H.2
  • 34
    • 0035930783 scopus 로고    scopus 로고
    • Expansion of structural and functional diversities of DNA using new 5-substituted deoxyuridine derivatives by PCR with superthermophilic KOD Dash DNA polymerase
    • Sawai, H., Ozaki, A. N., et al. Expansion of structural and functional diversities of DNA using new 5-substituted deoxyuridine derivatives by PCR with superthermophilic KOD Dash DNA polymerase. Chem. Commun. 2001, 2604-2605.
    • (2001) Chem. Commun. , pp. 2604-2605
    • Sawai, H.1    Ozaki, A.N.2
  • 35
    • 0036009644 scopus 로고    scopus 로고
    • Synthesis of new modified DNAs by hyperthermophilic DNA polymerase: Substrate and template specificity of functionalized thymidine analogues bearing an sp3-hybridized carbon at the C5 alpha-position for several DNA polyme-rases
    • Sawai, H., Ozaki-Nakamura, A., et al. Synthesis of new modified DNAs by hyperthermophilic DNA polymerase: Substrate and template specificity of functionalized thymidine analogues bearing an sp3-hybridized carbon at the C5 alpha-position for several DNA polyme-rases. Bioconj. Chem. 2002, 13 (2), 309-316.
    • (2002) Bioconj. Chem. , vol.13 , Issue.2 , pp. 309-316
    • Sawai, H.1    Ozaki-Nakamura, A.2
  • 36
    • 0141545111 scopus 로고    scopus 로고
    • Substrate properties of C5-substituted pyrimidine 20-deoxynucleoside 50-triphosphates for thermostable DNA polymerases during PCR
    • Kuwahara, M., Takahata, Y., et al. Substrate properties of C5-substituted pyrimidine 20-deoxynucleoside 50-triphosphates for thermostable DNA polymerases during PCR. Bioorg. Medicinal Chem. Lett. 2003, 13 (21), 3735-3738.
    • (2003) Bioorg. Medicinal Chem. Lett. , vol.13 , Issue.21 , pp. 3735-3738
    • Kuwahara, M.1    Takahata, Y.2
  • 37
    • 22744438967 scopus 로고    scopus 로고
    • Expansion of repertoire of modified DNAs prepared by PCR using KOD dash DNA polymerase
    • Ohbayashi, T., Kuwahara, M., et al. Expansion of repertoire of modified DNAs prepared by PCR using KOD dash DNA polymerase. Org. Biomol. Chem. 2005, 3 (13), 2463-2468.
    • (2005) Org. Biomol. Chem. , vol.3 , Issue.13 , pp. 2463-2468
    • Ohbayashi, T.1    Kuwahara, M.2
  • 38
    • 33644759249 scopus 로고    scopus 로고
    • Direct PCR amplification of various modified DNAs having amino acids: Convenient preparation of DNA libraries with highpotential activities for in vitro selection
    • Kuwahara, M., Hanawa, K., et al. Direct PCR amplification of various modified DNAs having amino acids: Convenient preparation of DNA libraries with highpotential activities for in vitro selection. Bioorg. Medicinal Chem. 2006, 14 (8), 2518-2526.
    • (2006) Bioorg. Medicinal Chem. , vol.14 , Issue.8 , pp. 2518-2526
    • Kuwahara, M.1    Hanawa, K.2
  • 39
    • 33750993500 scopus 로고    scopus 로고
    • Systematic characterization of 20-deoxynucleoside-50-triphosphate analogs as substrates for DNA polymerases by polymerase chain reaction and kinetic studies on enzymatic production of modified DNA
    • Kuwahara, M., Nagashima, J., et al. Systematic characterization of 20-deoxynucleoside-50-triphosphate analogs as substrates for DNA polymerases by polymerase chain reaction and kinetic studies on enzymatic production of modified DNA. Nucleic Acids Res. 2006, 34 (19), 5383-5394.
    • (2006) Nucleic Acids Res. , vol.34 , Issue.19 , pp. 5383-5394
    • Kuwahara, M.1    Nagashima, J.2
  • 40
    • 33846118875 scopus 로고    scopus 로고
    • Construction of saccharide-modified DNAs by DNA polymerase
    • Matsui, M., Nishiyama, Y., et al. Construction of saccharide-modified DNAs by DNA polymerase. Bioorg. Medicinal Chem. Lett. 2007, 17 (2), 456-460.
    • (2007) Bioorg. Medicinal Chem. Lett. , vol.17 , Issue.2 , pp. 456-460
    • Matsui, M.1    Nishiyama, Y.2
  • 41
    • 0035813885 scopus 로고    scopus 로고
    • Functionalized DNA: A new replicable biopolymer
    • Thum, O., Jager, S., et al. Functionalized DNA: A new replicable biopolymer. Angew. Chem.-Int. Ed. 2001, 40 (21), 3990-3993.
    • (2001) Angew. Chem.-Int. Ed. , vol.40 , Issue.21 , pp. 3990-3993
    • Thum, O.1    Jager, S.2
  • 42
    • 4544376496 scopus 로고    scopus 로고
    • Generation and enzymatic amplification of high-density functionalized DNA double strands
    • Jager, S. and Famulok, M. Generation and enzymatic amplification of high-density functionalized DNA double strands. Angew. Chem.-Int. Ed. 2004, 43 (25), 3337-3340.
    • (2004) Angew. Chem.-Int. Ed. , vol.43 , Issue.25 , pp. 3337-3340
    • Jager, S.1    Famulok, M.2
  • 43
    • 27544486140 scopus 로고    scopus 로고
    • A versatile toolbox for variable DNA functionalization at high density
    • Jager, S., Rasched, G., et al. A versatile toolbox for variable DNA functionalization at high density. J. Am. Chem. Soc. 2005, 127 (43), 15071-15082.
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.43 , pp. 15071-15082
    • Jager, S.1    Rasched, G.2
  • 44
    • 0029161984 scopus 로고
    • New uridine derivatives for systematic evolution of RNA ligands by exponential enrichment
    • Dewey, T. M., Mundt, A. A., et al. New uridine derivatives for systematic evolution of RNA ligands by exponential enrichment. J. Am. Chem. Soc. 1995, 117 (32), 8474-8475.
    • (1995) J. Am. Chem. Soc. , vol.117 , Issue.32 , pp. 8474-8475
    • Dewey, T.M.1    Mundt, A.A.2
  • 45
    • 4544246204 scopus 로고    scopus 로고
    • T7 RNA polymerase transcription with 5-position modified UTP derivatives
    • Vaught, J. D., Dewey, T., et al. T7 RNA polymerase transcription with 5-position modified UTP derivatives. J. Am. Chem. Soc. 2004, 126 (36), 11231-11237.
    • (2004) J. Am. Chem. Soc. , vol.126 , Issue.36 , pp. 11231-11237
    • Vaught, J.D.1    Dewey, T.2
  • 46
    • 0034284164 scopus 로고    scopus 로고
    • Expanding the structural and functional diversity of RNA: analog uridine triphosphates as candidates for in vitro selection of nucleic acids
    • Vaish, N. K., Fraley, A.W., et al. Expanding the structural and functional diversity of RNA: analog uridine triphosphates as candidates for in vitro selection of nucleic acids. Nucleic Acids Res. 2000, 28 (17), 3316-3322.
    • (2000) Nucleic Acids Res. , vol.28 , Issue.17 , pp. 3316-3322
    • Vaish, N.K.1    Fraley, A.W.2
  • 47
    • 0035901674 scopus 로고    scopus 로고
    • Highdensity labeling of DNA: Preparation and characterization of the target material for single-molecule sequencing
    • Brakmann, S. and Lobermann, S. Highdensity labeling of DNA: Preparation and characterization of the target material for single-molecule sequencing. Angew. Chem.-Int. Ed. 2001, 40 (8), 1427-1429.
    • (2001) Angew. Chem.-Int. Ed. , vol.40 , Issue.8 , pp. 1427-1429
    • Brakmann, S.1    Lobermann, S.2
  • 48
    • 0035496466 scopus 로고    scopus 로고
    • The large fragment of Escherichia coli DNA polymerase I can synthesize DNA exclusively from fluorescently labeled nucleotides
    • Brakmann, S. and Nieckchen, P. The large fragment of Escherichia coli DNA polymerase I can synthesize DNA exclusively from fluorescently labeled nucleotides. Chembiochem 2001, 2 (10), 773-777.
    • (2001) Chembiochem , vol.2 , Issue.10 , pp. 773-777
    • Brakmann, S.1    Nieckchen, P.2
  • 49
    • 0037009084 scopus 로고    scopus 로고
    • A further step towards single-molecule sequencing: Escherichia coli exonuclease III degrades DNA that is fluorescently labeled at each base pair
    • Brakmann, S. and Lobermann, S. A further step towards single-molecule sequencing: Escherichia coli exonuclease III degrades DNA that is fluorescently labeled at each base pair. Angew. Chem.-Int. Ed. 2002, 41 (17), 3215-3217.
    • (2002) Angew. Chem.-Int. Ed. , vol.41 , Issue.17 , pp. 3215-3217
    • Brakmann, S.1    Lobermann, S.2
  • 50
    • 0037156350 scopus 로고    scopus 로고
    • Enzymatic synthesis of labeled DNA by PCR using new fluorescent thymidine nucleotide analogue and superthermophilicKOD DashDNApolymerase
    • Obayashi, T., Masud, M. M., et al. Enzymatic synthesis of labeled DNA by PCR using new fluorescent thymidine nucleotide analogue and superthermophilicKOD DashDNApolymerase. Bioorg. Medicinal Chem. Lett. 2002, 12 (8), 1167-1170.
    • (2002) Bioorg. Medicinal Chem. Lett. , vol.12 , Issue.8 , pp. 1167-1170
    • Obayashi, T.1    Masud, M.M.2
  • 51
    • 0037705457 scopus 로고    scopus 로고
    • Incorporation of reporter molecule-labeled nucleotides by DNA polymerase. I. Chemical synthesis of various reporter group-labeled 20-deoxyribonucleoside-50-triphosphates
    • Giller, G., Tasara, T., et al. Incorporation of reporter molecule-labeled nucleotides by DNA polymerase. I. Chemical synthesis of various reporter group-labeled 20-deoxyribonucleoside-50-triphosphates. Nucleic Acids Res. 2003, 31 (10), 2630-2635.
    • (2003) Nucleic Acids Res. , vol.31 , Issue.10 , pp. 2630-2635
    • Giller, G.1    Tasara, T.2
  • 52
    • 0037705455 scopus 로고    scopus 로고
    • Incorporation of reporter molecule-labeled nucleotides by DNA polymerases. II. High-density labeling of natural DNA
    • Tasara, T., Angerer, B., et al. Incorporation of reporter molecule-labeled nucleotides by DNA polymerases. II. High-density labeling of natural DNA. Nucleic Acids Res. 2003, 31 (10), 2636-2646.
    • (2003) Nucleic Acids Res. , vol.31 , Issue.10 , pp. 2636-2646
    • Tasara, T.1    Angerer, B.2
  • 53
    • 13444255987 scopus 로고    scopus 로고
    • Incorporation of reporter-labeled nucleotides by DNA polymerases
    • Anderson, J. P., Angerer, B., et al. Incorporation of reporter-labeled nucleotides by DNA polymerases. Biotechniques 2005, 38 (2), 257-264.
    • (2005) Biotechniques , vol.38 , Issue.2 , pp. 257-264
    • Anderson, J.P.1    Angerer, B.2
  • 54
    • 0032122430 scopus 로고    scopus 로고
    • Hybridization properties of base-modified oligonucleotides within the double and triple helix motif
    • Luyten, I. and Herdewijn, P. Hybridization properties of base-modified oligonucleotides within the double and triple helix motif. Eur. J. Medicinal Chem. 1998, 33 (7-8), 515-576.
    • (1998) Eur. J. Medicinal Chem. , vol.33 , Issue.7-8 , pp. 515-576
    • Luyten, I.1    Herdewijn, P.2
  • 55
    • 0026783155 scopus 로고
    • Oligodeoxynucleotides containing C-5 propyne analogs of 20-deoxyuridine and 20-deoxycytidine
    • Froehler, B. C., Wadwani, S., et al. Oligodeoxynucleotides containing C-5 propyne analogs of 20-deoxyuridine and 20-deoxycytidine. Tetrahedron Lett. 1992, 33 (37), 5307-5310.
    • (1992) Tetrahedron Lett. , vol.33 , Issue.37 , pp. 5307-5310
    • Froehler, B.C.1    Wadwani, S.2
  • 56
    • 0027246678 scopus 로고
    • Antisense gene inhibition by oligonucleotides containing C-5 propyne pyrimidines
    • Wagner, R. W., Matteucci, M. D., et al. Antisense gene inhibition by oligonucleotides containing C-5 propyne pyrimidines. Science 1993, 260 (5113), 1510-1513.
    • (1993) Science , vol.260 , Issue.5113 , pp. 1510-1513
    • Wagner, R.W.1    Matteucci, M.D.2
  • 57
    • 0029943016 scopus 로고    scopus 로고
    • Potent and selective inhibition of gene expression by an antisense heptanucleo-tide
    • Wagner, R. W., Matteucci, M. D., et al. Potent and selective inhibition of gene expression by an antisense heptanucleo-tide. Nature Biotechnol 1996, 14, 840-844.
    • (1996) Nature Biotechnol , vol.14 , pp. 840-844
    • Wagner, R.W.1    Matteucci, M.D.2
  • 58
    • 0034794425 scopus 로고    scopus 로고
    • Long-range cooperativity in molecular recognition of RNA by oligodeoxynucleotides, with multiple C5-(1-propynyl) pyrimidines
    • Barnes, T.W. and Turner, D.H. Long-range cooperativity in molecular recognition of RNA by oligodeoxynucleotides, with multiple C5-(1-propynyl) pyrimidines. J. Am. Chem. Soc. 2001, 123 (18), 4107-4118.
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.18 , pp. 4107-4118
    • Barnes, T.W.1    Turner, D.H.2
  • 59
    • 0035913728 scopus 로고    scopus 로고
    • Long-range cooperativity due to C5-propynylation of oligopyrimidines enhances specific recognition by uridine of ribo-adenosine over ribo-guanosine
    • Barnes, T. W. and Turner, D. L. H. Long-range cooperativity due to C5-propynylation of oligopyrimidines enhances specific recognition by uridine of ribo-adenosine over ribo-guanosine. J. Am. Chem. Soc. 2001, 123 (37), 9186-9187.
    • (2001) J. Am. Chem. Soc. , vol.123 , Issue.37 , pp. 9186-9187
    • Barnes, T.W.1    Turner, D.L.H.2
  • 60
    • 0035940485 scopus 로고    scopus 로고
    • C5-(1-Propynyl)-20-deoxy-pyrimidines enhance mismatch penalties of DNA: RNA duplex formation
    • Barnes, T. W. and Turner, D. H. C5-(1-Propynyl)-20-deoxy-pyrimidines enhance mismatch penalties of DNA: RNA duplex formation. Biochemistry 2001, 40 (42), 12738-12745.
    • (2001) Biochemistry , vol.40 , Issue.42 , pp. 12738-12745
    • Barnes, T.W.1    Turner, D.H.2
  • 61
    • 0038043309 scopus 로고    scopus 로고
    • The solution structure of aDNAcenter dot RNA duplex containing 5-propynyl U and C; comparison with 5-Me modifications
    • Gyi, J. I., Gao, D. Q., et al. The solution structure of aDNAcenter dot RNA duplex containing 5-propynyl U and C; comparison with 5-Me modifications. Nucleic Acids Res. 2003, 31 (10), 2683-2693.
    • (2003) Nucleic Acids Res. , vol.31 , Issue.10 , pp. 2683-2693
    • Gyi, J.I.1    Gao, D.Q.2
  • 62
    • 0015911780 scopus 로고
    • 5-(4-Aminobutylamino)uracil, an unusual pyrimidine from the deoxyribonucleic acid of bacteriophage phiW-14
    • Kropinski, A. M. B., Bose, R. J., et al. 5-(4-Aminobutylamino)uracil, an unusual pyrimidine from the deoxyribonucleic acid of bacteriophage phiW-14. Biochemistry 1973, 12 (1), 151-157.
    • (1973) Biochemistry , vol.12 , Issue.1 , pp. 151-157
    • Kropinski, A.M.B.1    Bose, R.J.2
  • 63
    • 0023552056 scopus 로고
    • Synthesis and properties of deoxyribonucleotides containing putrescinylthymine (Nucleosides and Nucleotides LXXVI)
    • Takeda, T., Ikeda, K., et al. Synthesis and properties of deoxyribonucleotides containing putrescinylthymine (Nucleosides and Nucleotides LXXVI). Chem. Pharm. Bull. 1987, 35 (9), 3558-3567.
    • (1987) Chem. Pharm. Bull. , vol.35 , Issue.9 , pp. 3558-3567
    • Takeda, T.1    Ikeda, K.2
  • 64
    • 0000717784 scopus 로고
    • Formation of chimeric duplexes between zwitterionic and natural DNA
    • Hashimoto, H., Nelson, M. G., et al. Formation of chimeric duplexes between zwitterionic and natural DNA. J. Org. Chem. 1993, 58 (16), 4194-4195.
    • (1993) J. Org. Chem. , vol.58 , Issue.16 , pp. 4194-4195
    • Hashimoto, H.1    Nelson, M.G.2
  • 65
    • 0001193158 scopus 로고
    • Zwitterionic DNA
    • Hashimoto, H., Nelson, M. G., et al. Zwitterionic DNA. J. Am. Chem. Soc. 1993, 115 (16), 7128-7134.
    • (1993) J. Am. Chem. Soc. , vol.115 , Issue.16 , pp. 7128-7134
    • Hashimoto, H.1    Nelson, M.G.2
  • 66
    • 0029138771 scopus 로고
    • Nucleosides and nucleotid. 135. DNA duplex and triplex formation and resistance to nucleolytic degradation of oligodeoxynucleotides containing syn-norspermidine at the 5-position of 20-deoxyuridine
    • Nara, H., Ono, A., et al. Nucleosides and nucleotid. 135. DNA duplex and triplex formation and resistance to nucleolytic degradation of oligodeoxynucleotides containing syn-norspermidine at the 5-position of 20-deoxyuridine. Bioconj. Chem. 1995, 6 (1), 54-61.
    • (1995) Bioconj. Chem. , vol.6 , Issue.1 , pp. 54-61
    • Nara, H.1    Ono, A.2
  • 67
    • 0029150305 scopus 로고
    • Novel C5-substituted 20-deoxyuridine derivatives bearing amino-linker arms-synthesis, incorporation into oligodeoxyribonucleotides, and their hybridization properties
    • Ozaki, H., Nakamura, A., et al. Novel C5-substituted 20-deoxyuridine derivatives bearing amino-linker arms-synthesis, incorporation into oligodeoxyribonucleotides, and their hybridization properties. Bull. Chem. Soc. Japan 1995, 68 (7), 1981-1987.
    • (1995) Bull. Chem. Soc. Japan , vol.68 , Issue.7 , pp. 1981-1987
    • Ozaki, H.1    Nakamura, A.2
  • 68
    • 0031937077 scopus 로고    scopus 로고
    • Nucleosides and nucleotides. 165. Chemical ligation of oligodeoxynucleotides having a mercapto group at the 5-position of 20-deoxyuridine via a disulfide bond
    • Ueno, Y., Nakagawa, A., et al. Nucleosides and nucleotides. 165. Chemical ligation of oligodeoxynucleotides having a mercapto group at the 5-position of 20-deoxyuridine via a disulfide bond. Nucleosides Nucleotides 1998, 17 (1-3), 283-289.
    • (1998) Nucleosides Nucleotides , vol.17 , Issue.1-3 , pp. 283-289
    • Ueno, Y.1    Nakagawa, A.2
  • 69
    • 0035572969 scopus 로고    scopus 로고
    • Effect of the terminal amino group of a linker arm and its length at the C5 position of a pyrimidine nucleoside on the thermal stability of DNA duplexes
    • Ozaki, H., Mine, M., et al. Effect of the terminal amino group of a linker arm and its length at the C5 position of a pyrimidine nucleoside on the thermal stability of DNA duplexes. Bioorg. Chem. 2001, 29 (4), 187-197.
    • (2001) Bioorg. Chem. , vol.29 , Issue.4 , pp. 187-197
    • Ozaki, H.1    Mine, M.2
  • 70
    • 0038719822 scopus 로고    scopus 로고
    • Synthesis, thermal stability and resistance to enzymatic hydrolysis of the oligonucleotides containing 5-(N-aminohexyl)carbamoyl-20-O-methyluridines
    • Ito, T., Ueno, Y., et al. Synthesis, thermal stability and resistance to enzymatic hydrolysis of the oligonucleotides containing 5-(N-aminohexyl)carbamoyl-20-O-methyluridines. Nucleic Acids Res. 2003, 31 (10), 2514-2523.
    • (2003) Nucleic Acids Res. , vol.31 , Issue.10 , pp. 2514-2523
    • Ito, T.1    Ueno, Y.2
  • 71
    • 1542574144 scopus 로고    scopus 로고
    • Effect of imino group of a linker armat the C5 position of a pyrimidine nucleoside on the thermal stabilities of DNA/DNA and DNA/RNA duplexes
    • Ozaki, H., Mine, M., et al. Effect of imino group of a linker armat the C5 position of a pyrimidine nucleoside on the thermal stabilities of DNA/DNA and DNA/RNA duplexes. Nucleosides Nucleotides Nucleic Acids 2004, 23 (1-2), 339-346.
    • (2004) Nucleosides Nucleotides Nucleic Acids , vol.23 , Issue.1-2 , pp. 339-346
    • Ozaki, H.1    Mine, M.2
  • 72
    • 34247895758 scopus 로고    scopus 로고
    • Crystal structures of DNA:DNA and DNA:RNA duplexes containing 5-(N-aminohexyl) carbamoyl-modified uracils reveal the basis for properties as antigene and antisense molecules
    • Juan, E. C. M., Kondo, J., et al. Crystal structures of DNA:DNA and DNA:RNA duplexes containing 5-(N-aminohexyl) carbamoyl-modified uracils reveal the basis for properties as antigene and antisense molecules. Nucleic Acids Res. 2007, 35 (6), 1969-1977.
    • (2007) Nucleic Acids Res. , vol.35 , Issue.6 , pp. 1969-1977
    • Juan, E.C.M.1    Kondo, J.2
  • 73
    • 0037027362 scopus 로고    scopus 로고
    • Effect of cationic charge localization on DNAstructure
    • Gold, B. Effect of cationic charge localization on DNAstructure. Biopolymers 2002, 65 (3), 173-179.
    • (2002) Biopolymers , vol.65 , Issue.3 , pp. 173-179
    • Gold, B.1
  • 74
    • 0037166983 scopus 로고    scopus 로고
    • Structure of a tethered cationic 3-aminopropyl chain incorporated into an oligodeoxynucleotide: Evidence for 30-orientation in the major groove accompanied by DNA bending
    • Li, Z. J., Huang, L., et al. Structure of a tethered cationic 3-aminopropyl chain incorporated into an oligodeoxynucleotide: Evidence for 30-orientation in the major groove accompanied by DNA bending. J.Am. Chem. Soc. 2002, 124 (29), 8553-8560.
    • (2002) J.Am. Chem. Soc. , vol.124 , Issue.29 , pp. 8553-8560
    • Li, Z.J.1    Huang, L.2
  • 75
    • 21044448039 scopus 로고    scopus 로고
    • Structure of B-DNA with cations tethered in the major groove
    • Moulaei, T., Maehigashi, T., et al. Structure of B-DNA with cations tethered in the major groove. Biochemistry 2005, 44 (20), 7458-7468.
    • (2005) Biochemistry , vol.44 , Issue.20 , pp. 7458-7468
    • Moulaei, T.1    Maehigashi, T.2
  • 76
    • 24944523204 scopus 로고    scopus 로고
    • Incorporation of cationic chains in the Dickerson-Drew dodecamer: Correlation of energetics, structure, and ion and water binding
    • Shikiya, R., Li, J. S., et al. Incorporation of cationic chains in the Dickerson-Drew dodecamer: Correlation of energetics, structure, and ion and water binding. Biochemistry 2005, 44 (37), 12582-12588.
    • (2005) Biochemistry , vol.44 , Issue.37 , pp. 12582-12588
    • Shikiya, R.1    Li, J.S.2
  • 77
    • 15444368861 scopus 로고    scopus 로고
    • Determining the origin of the stabilization of DNA by 5-aminopropynylation of pyrimidines
    • Booth, J., Brown, T., et al. Determining the origin of the stabilization of DNA by 5-aminopropynylation of pyrimidines. Biochemistry 2005, 44 (12), 4710-4719.
    • (2005) Biochemistry , vol.44 , Issue.12 , pp. 4710-4719
    • Booth, J.1    Brown, T.2
  • 78
    • 27444444758 scopus 로고    scopus 로고
    • Nucleic acid with guanidinium modification exhibits efficient cellular uptake
    • Ohmichi, T., Kuwahara, M., et al. Nucleic acid with guanidinium modification exhibits efficient cellular uptake. Angew. Chem.-Int. Ed. 2005, 44 (41), 6682-6685.
    • (2005) Angew. Chem.-Int. Ed. , vol.44 , Issue.41 , pp. 6682-6685
    • Ohmichi, T.1    Kuwahara, M.2
  • 79
    • 33645775235 scopus 로고    scopus 로고
    • Impact of the guanidinium group on hybridization and cellular uptake of cationic oligonucleotides
    • Deglane, G., Abes, S., et al. Impact of the guanidinium group on hybridization and cellular uptake of cationic oligonucleotides. Chembiochem 2006, 7 (4), 684-692.
    • (2006) Chembiochem , vol.7 , Issue.4 , pp. 684-692
    • Deglane, G.1    Abes, S.2
  • 80
    • 22244439863 scopus 로고    scopus 로고
    • Templatedirected DNA photoligation via alpha-5-cyanovinyldeoxyuridine
    • Ogino, M., Yoshimura, Y., et al. Templatedirected DNA photoligation via alpha-5-cyanovinyldeoxyuridine. Org. Lett. 2005, 7 (14), 2853-2856.
    • (2005) Org. Lett. , vol.7 , Issue.14 , pp. 2853-2856
    • Ogino, M.1    Yoshimura, Y.2
  • 81
    • 33750907113 scopus 로고    scopus 로고
    • Highly selective and sensitive template-directed photoligation of DNA via 5-carbamoylvinyl-20-deoxycytidine
    • Yoshimura, Y., Okamura, D., et al. Highly selective and sensitive template-directed photoligation of DNA via 5-carbamoylvinyl-20-deoxycytidine. Org.Lett. 2006, 8 (22), 5049-5051.
    • (2006) Org.Lett. , vol.8 , Issue.22 , pp. 5049-5051
    • Yoshimura, Y.1    Okamura, D.2
  • 82
    • 33845528995 scopus 로고    scopus 로고
    • Highly sequence specific RNA terminal labeling by DNA photoligation
    • Yoshimura, Y., Noguchi, Y., et al. Highly sequence specific RNA terminal labeling by DNA photoligation. Org. Biomol. Chem. 2007, 5 (1), 139-142.
    • (2007) Org. Biomol. Chem. , vol.5 , Issue.1 , pp. 139-142
    • Yoshimura, Y.1    Noguchi, Y.2
  • 83
    • 0034597975 scopus 로고    scopus 로고
    • Template directed photochemical synthesis of branched oligodeoxynucle-otides via 5-carboxyvinyldeoxyuridine
    • Fujimoto, K., Ogawa, N., et al. Template directed photochemical synthesis of branched oligodeoxynucle-otides via 5-carboxyvinyldeoxyuridine. Tetrahedron Lett. 2000, 41 (49), 9437-9440.
    • (2000) Tetrahedron Lett. , vol.41 , Issue.49 , pp. 9437-9440
    • Fujimoto, K.1    Ogawa, N.2
  • 84
    • 26944447111 scopus 로고    scopus 로고
    • A novel method to synthesize versatile multiplebranched DNA (MB-DNA) by reversible photochemical ligation
    • Ogasawara, S. and Fujimoto, K. A novel method to synthesize versatile multiplebranched DNA (MB-DNA) by reversible photochemical ligation. Chembiochem 2005, 6 (10), 1756-1760.
    • (2005) Chembiochem , vol.6 , Issue.10 , pp. 1756-1760
    • Ogasawara, S.1    Fujimoto, K.2
  • 85
    • 19444387597 scopus 로고    scopus 로고
    • Solution of a SAT problem on a photochemical DNA computer
    • Ogasawara, S. and Fujimoto, K. Solution of a SAT problem on a photochemical DNA computer. Chem. Lett. 2005, 34 (3), 378-379.
    • (2005) Chem. Lett. , vol.34 , Issue.3 , pp. 378-379
    • Ogasawara, S.1    Fujimoto, K.2
  • 86
    • 33746385381 scopus 로고    scopus 로고
    • Sitespecific transition of cytosine to uracil via reversible DNA photoligation
    • Fujimoto, K., Matsuda, S., et al. Sitespecific transition of cytosine to uracil via reversible DNA photoligation. Chem. Commun. 2006, 3223-3225.
    • (2006) Chem. Commun. , pp. 3223-3225
    • Fujimoto, K.1    Matsuda, S.2
  • 87
    • 22344437947 scopus 로고    scopus 로고
    • Photoinduced DNA end capping via N-3-methyl-5-cyanovinyl-20-deoxyuridine
    • Fujimoto, K., Yoshimura, Y., et al. Photoinduced DNA end capping via N-3-methyl-5-cyanovinyl-20-deoxyuridine. Chem. Commun. 2005, 3177-3179.
    • (2005) Chem. Commun. , pp. 3177-3179
    • Fujimoto, K.1    Yoshimura, Y.2
  • 88
    • 9944239848 scopus 로고    scopus 로고
    • Templatedirected photoreversible ligation of DNA via 7-carboxyvinyl-7-deaza-20-deoxyadenosine
    • Saito, I., Miyauchi, Y., et al. Templatedirected photoreversible ligation of DNA via 7-carboxyvinyl-7-deaza-20-deoxyadenosine. Tetrahedron Lett. 2005, 46 (1), 97-99.
    • (2005) Tetrahedron Lett. , vol.46 , Issue.1 , pp. 97-99
    • Saito, I.1    Miyauchi, Y.2
  • 89
    • 1142306164 scopus 로고    scopus 로고
    • Site-specific incorporation of a photo-crosslinking component into RNA by T7 transcription mediated by unnatural basepairs
    • Kimoto, M., Endo, M., et al. Site-specific incorporation of a photo-crosslinking component into RNA by T7 transcription mediated by unnatural basepairs. Chemistry Biology 2004, 11 (1), 47-55.
    • (2004) Chemistry Biology , vol.11 , Issue.1 , pp. 47-55
    • Kimoto, M.1    Endo, M.2
  • 90
    • 33745580307 scopus 로고    scopus 로고
    • Facile photocyclization chemistry of 5-phenylthio-20-deoxyuridine in duplex DNA
    • Zeng, Y., Cao, H. C., et al. Facile photocyclization chemistry of 5-phenylthio-20-deoxyuridine in duplex DNA. Org. Lett. 2006, 8 (12), 2527-2530.
    • (2006) Org. Lett. , vol.8 , Issue.12 , pp. 2527-2530
    • Zeng, Y.1    Cao, H.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.