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Volumn 16, Issue 2, 2012, Pages 161-223

7-deazapurine (Pyrrolo[2,3-d]Pyrimidine) 2'-deoxyribonucleosides: Syntheses and transformations

Author keywords

7 deazapurine; Click reaction; Cross coupling; Enantiomers; Glycosylation; Halogenation; Nucleosides; Pyrrolo 2,3 d pyrimidines; Sequencing; Triphosphates

Indexed keywords

AROMATIC COMPOUNDS; BIOMOLECULES; COPPER COMPOUNDS; DNA SEQUENCES; ENANTIOMERS; GENE ENCODING;

EID: 84856457711     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527212798993086     Document Type: Review
Times cited : (27)

References (290)
  • 2
    • 28244462818 scopus 로고    scopus 로고
    • Fluorescence based strategies for genetic analysis
    • Ranasinghe, R. T.; Brown, T. Fluorescence based strategies for genetic analysis. Chem. Commun., 2005, 5487-5502.
    • (2005) Chem. Commun. , pp. 5487-5502
    • Ranasinghe, R.T.1    Brown, T.2
  • 7
    • 0016804870 scopus 로고
    • Structure of the modified nucleoside Q isolated from Escherichia coli transfer ribonucleic acid. 7-(4,5-cis-Dihydroxy-1-cyclopenten-3-ylaminomethyl)-7-deazaguanosine
    • Kasai, H.; Ohashi, Z.; Harada, F.; Nishimura, S.; Oppenheimer, N. J.; Crain, P. F.; Liehr, J. G.; von Minden, D. L.; McCloskey, J. A. Structure of the modified nucleoside Q isolated from Escherichia coli transfer ribonucleic acid. 7-(4,5-cis-Dihydroxy-1-cyclopenten-3-ylaminomethyl)-7-deazaguanosine. Biochemistry, 1975, 14(19), 4198-4208.
    • (1975) Biochemistry , vol.14 , Issue.19 , pp. 4198-4208
    • Kasai, H.1    Ohashi, Z.2    Harada, F.3    Nishimura, S.4    Oppenheimer, N.J.5    Crain, P.F.6    Liehr, J.G.7    von Minden, D.L.8    McCloskey, J.A.9
  • 8
    • 0346354082 scopus 로고
    • Kanagawamicin, a new aminonucleoside analog antibiotic from actinoplanes kanagawaensis
    • Naruto, S.; Uno, H.; Tanaka, A.; Kotani, H.; Takase, Y. Kanagawamicin, a new aminonucleoside analog antibiotic from actinoplanes kanagawaensis. Heterocyles, 1983, 20(1), 27-32.
    • (1983) Heterocyles , vol.20 , Issue.1 , pp. 27-32
    • Naruto, S.1    Uno, H.2    Tanaka, A.3    Kotani, H.4    Takase, Y.5
  • 10
    • 0021842569 scopus 로고
    • Bioactive marine metabolites IX. Mycalisines A and B, novel nucleosides which inhibit cell division of fertilized starfish eggs, from the marine sponge mycale sp
    • Kato, Y.; Fusetani, N.; Matsunaga, S.; Hashimoto, K. Bioactive marine metabolites IX. Mycalisines A and B, novel nucleosides which inhibit cell division of fertilized starfish eggs, from the marine sponge mycale sp. Tetrahedron Lett., 1985, 26(29), 3483-3486.
    • (1985) Tetrahedron Lett , vol.26 , Issue.29 , pp. 3483-3486
    • Kato, Y.1    Fusetani, N.2    Matsunaga, S.3    Hashimoto, K.4
  • 11
    • 0020494583 scopus 로고
    • Poly(7-deazaguanylic acid), the homopolynucleotide of the parent nucleoside of queuosine
    • Seela, F.; Tran-Thi, Q.-H.; Franzen, D. Poly(7-deazaguanylic acid), the homopolynucleotide of the parent nucleoside of queuosine. Biochemistry, 1982, 21(18), 4338-4343.
    • (1982) Biochemistry , vol.21 , Issue.18 , pp. 4338-4343
    • Seela, F.1    Tran-Thi, Q.-H.2    Franzen, D.3
  • 12
    • 33744486432 scopus 로고    scopus 로고
    • Base-Modified Oligodeoxyribonucleotides: Using Pyrrolo[2,3-d] pyrimidines to Replace Purines
    • Harkins, E. W., Ed. John Wiley & Sons
    • Seela, F.; Peng, X. Base-Modified Oligodeoxyribonucleotides: Using Pyrrolo[2,3-d] pyrimidines to Replace Purines. In: Current Protocols in Nucleic Acid Chemistry; Harkins, E. W., Ed. John Wiley & Sons: 2005; Vol. 1, pp. 4.25.1-4.25.25.
    • (2005) Current Protocols in Nucleic Acid Chemistry , vol.1 , pp. 1-25
    • Seela, F.1    Peng, X.2
  • 13
    • 0014965547 scopus 로고
    • Crystal and molecular structure of 8-bromoguanosine and 8-bromoadenosine, two purine nucleosides in the syn conformation
    • Tavale, S. S.; Sobell, H. M. Crystal and molecular structure of 8-bromoguanosine and 8-bromoadenosine, two purine nucleosides in the syn conformation. J. Mol. Biol., 1970, 48(1), 109-123.
    • (1970) J. Mol. Biol. , vol.48 , Issue.1 , pp. 109-123
    • Tavale, S.S.1    Sobell, H.M.2
  • 14
    • 0021772481 scopus 로고
    • Poly(8-bromodeoxyadenylic acid): Properties of the polymer and contrast with the ribopolynucleotide analogue
    • Kanaya, E. N.; Howard, F. B.; Frazier, J.; Miles, H. T. Poly(8-bromodeoxyadenylic acid): properties of the polymer and contrast with the ribopolynucleotide analogue. Biochemistry, 1984, 23(18), 4219-4225.
    • (1984) Biochemistry , vol.23 , Issue.18 , pp. 4219-4225
    • Kanaya, E.N.1    Howard, F.B.2    Frazier, J.3    Miles, H.T.4
  • 15
    • 0030007499 scopus 로고    scopus 로고
    • Synthesis structure and thermodynamic properties of 8-methylguanine-containing oligonucleotides: Z-DNA under physiological salt conditions
    • Sugiyama, H.; Kawai, K.; Matsunaga, A.; Fujimoto, K.; Saito, I.; Robinson, H.; Wang, A. H.-J. Synthesis, structure and thermodynamic properties of 8-methylguanine-containing oligonucleotides: Z-DNA under physiological salt conditions. Nucleic Acids Res., 1996, 24(7), 1272-1278.
    • (1996) Nucleic Acids Res , vol.24 , Issue.7 , pp. 1272-1278
    • Sugiyama, H.1    Kawai, K.2    Matsunaga, A.3    Fujimoto, K.4    Saito, I.5    Robinson, H.6    Wang, A.H.-J.7
  • 16
    • 0026500030 scopus 로고
    • dTP incorporation during PCR-amplification and protection from endodeoxyribonuclease hydrolysis
    • dTP incorporation during PCR-amplification and protection from endodeoxyribonuclease hydrolysis. Nucleic Acids Res., 1992, 20(1), 55-61.
    • (1992) Nucleic Acids Res , vol.20 , Issue.1 , pp. 55-61
    • Seela, F.1    Röling, A.2
  • 17
    • 0026323195 scopus 로고
    • DNA-fragments resistant to endodeoxyribonuclease hydrolysis PCR-amplification using 7-deaza-2'-deoxyguanosine triphosphate in place of dGTP
    • Seela, F.; Röling, A. DNA-fragments resistant to endodeoxyribonuclease hydrolysis PCR-amplification using 7-deaza-2'-deoxyguanosine triphosphate in place of dGTP. Nucleosides Nucleotides, 1991, 10(1), 715-717.
    • (1991) Nucleosides Nucleotides , vol.10 , Issue.1 , pp. 715-717
    • Seela, F.1    Röling, A.2
  • 18
    • 0035853639 scopus 로고    scopus 로고
    • Fluorescent DNA: The development of 7-deazapurine nucleoside triphosphates applicable for sequencing at the single molecule level
    • Seela, F.; Feiling, E.; Gross, J.; Hillenkamp, F.; Ramzaeva, N.; Rosemeyer, H.; Zulauf, M. Fluorescent DNA: the development of 7-deazapurine nucleoside triphosphates applicable for sequencing at the single molecule level. J. Biotechnol., 2001, 86(3), 269-279.
    • (2001) J. Biotechnol. , vol.86 , Issue.3 , pp. 269-279
    • Seela, F.1    Feiling, E.2    Gross, J.3    Hillenkamp, F.4    Ramzaeva, N.5    Rosemeyer, H.6    Zulauf, M.7
  • 19
    • 0022596118 scopus 로고
    • Improvement of the dideoxy chain termination method of DNA sequencing by use of deoxy-7-deazaguanosine triphosphate in place of dGTP
    • Mizusawa, S.; Nishimura, S.; Seela, F. Improvement of the dideoxy chain termination method of DNA sequencing by use of deoxy-7-deazaguanosine triphosphate in place of dGTP. Nucleic Acids Res., 1986, 14(3), 1319-1324.
    • (1986) Nucleic Acids Res , vol.14 , Issue.3 , pp. 1319-1324
    • Mizusawa, S.1    Nishimura, S.2    Seela, F.3
  • 20
    • 0008160501 scopus 로고
    • 7-Deaza-2'-deoxyguanosine-5'-triphosphate: Enhanced resolution in M13 dideoxy Sequencing
    • Barr, P. J.; Thayer, R. M.; Laybourn, P.; Najarian, R. C.; Seela, F.; Tolan, D. R. 7-Deaza-2'-deoxyguanosine-5'-triphosphate: enhanced resolution in M13 dideoxy Sequencing. BioTechniques, 1986, 4(5), 428-432.
    • (1986) BioTechniques , vol.4 , Issue.5 , pp. 428-432
    • Barr, P.J.1    Thayer, R.M.2    Laybourn, P.3    Najarian, R.C.4    Seela, F.5    Tolan, D.R.6
  • 22
    • 0023684367 scopus 로고
    • Total synthesis of 7-iodo-2',3'-dideoxy-7-deazapurine nucleosides, key intermediates in the preparation of reagents for the automated sequencing of DNA
    • Cocuzza, A. J. Total synthesis of 7-iodo-2',3'-dideoxy-7-deazapurine nucleosides, key intermediates in the preparation of reagents for the automated sequencing of DNA. Tetrahedron Lett., 1988, 29(33), 4061-4064.
    • (1988) Tetrahedron Lett , vol.29 , Issue.33 , pp. 4061-4064
    • Cocuzza, A.J.1
  • 23
    • 37049084703 scopus 로고
    • Furanoside-pyranoside isomerization of tubercidin and its 2'-deoxy derivatives: Influence of nucleobase and sugar structure on the proton-catalysed reaction
    • Seela, F.; Menkhoff, S.; Behrendt, S. Furanoside-pyranoside isomerization of tubercidin and its 2'-deoxy derivatives: influence of nucleobase and sugar structure on the proton-catalysed reaction. J. Chem. Soc., Perkin Trans. 2, 1986, 525-530.
    • (1986) J. Chem. Soc., Perkin Trans. , vol.2 , pp. 525-530
    • Seela, F.1    Menkhoff, S.2    Behrendt, S.3
  • 24
    • 41149095126 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of 7-deaza cyclic adenosine 5'-diphosphate ribose analogues, membranepermeant modulators of intracellular calcium release
    • Zhang, B.; Bailey, V. C.; Potter, B. V. L. Chemoenzymatic synthesis of 7-deaza cyclic adenosine 5'-diphosphate ribose analogues, membranepermeant modulators of intracellular calcium release. J. Org. Chem., 2008, 73(5), 1693-1703.
    • (2008) J. Org. Chem. , vol.73 , Issue.5 , pp. 1693-1703
    • Zhang, B.1    Bailey, V.C.2    Potter, B.V.L.3
  • 25
    • 0029073182 scopus 로고
    • Increased stability of nucleic acids containing 7-deaza-guanosine and 7-deaza-adenosine may enable rapid DNA sequencing by matrix-assisted laser desorption mass spectrometry
    • Schneider, K.; Chait, B. T. Increased stability of nucleic acids containing 7-deaza-guanosine and 7-deaza-adenosine may enable rapid DNA sequencing by matrix-assisted laser desorption mass spectrometry. Nucleic Acids Res., 1995, 23(9), 1570-1575.
    • (1995) Nucleic Acids Res , vol.23 , Issue.9 , pp. 1570-1575
    • Schneider, K.1    Chait, B.T.2
  • 26
    • 8844241600 scopus 로고    scopus 로고
    • Fluorescence quenching of parallel-stranded DNA bound ethidium bromide: The effect of 7-deaza-2'-deoxyisoguanosine and 7-halogenated derivatives
    • Li, H.; Peng, X.; Seela, F. Fluorescence quenching of parallel-stranded DNA bound ethidium bromide: the effect of 7-deaza-2'-deoxyisoguanosine and 7-halogenated derivatives. Biorg. Med. Chem. Lett., 2004, 14(24), 6031-6034.
    • (2004) Biorg. Med. Chem. Lett. , vol.14 , Issue.24 , pp. 6031-6034
    • Li, H.1    Peng, X.2    Seela, F.3
  • 27
    • 0025861617 scopus 로고
    • Ethidium bromide does not fluoresce when intercalated adjacent to 7-deazaguanine in duplex DNA
    • Latimer, L. J. P.; Lee, J. S. Ethidium bromide does not fluoresce when intercalated adjacent to 7-deazaguanine in duplex DNA. J. Biol. Chem., 1991, 266(21), 13849-13851.
    • (1991) J. Biol. Chem. , vol.266 , Issue.21 , pp. 13849-13851
    • Latimer, L.J.P.1    Lee, J.S.2
  • 29
    • 84986481904 scopus 로고
    • A survey of methods for the preparation of pyrrolopyrimidines
    • Amarnath, V.; Madhav, R. A survey of methods for the preparation of pyrrolopyrimidines. Synthesis, 1974, 837-859.
    • (1974) Synthesis , pp. 837-859
    • Amarnath, V.1    Madhav, R.2
  • 30
    • 33744486432 scopus 로고    scopus 로고
    • Synthesis and Properties of 7-Substituted 7-Deazapurine (Pyrrolo[2,3-d]pyrimidine) 2'-Deoxyribonucleosides
    • Harkins, E. W., Ed.; John Wiley & Sons
    • Seela, F.; Peng, X. Synthesis and Properties of 7-Substituted 7-Deazapurine (Pyrrolo[2,3-d]pyrimidine) 2'-Deoxyribonucleosides. In: Current Protocols in Nucleic Acid Chemistry; Harkins, E. W., Ed.; John Wiley & Sons: 2005; Vol. 1, pp. 1.10.1-1.10.20.
    • (2005) Current Protocols in Nucleic Acid Chemistry Ed , vol.1 , pp. 1-20
    • Seela, F.1    Peng, X.2
  • 31
    • 33744490082 scopus 로고    scopus 로고
    • Progress in 7-deazapurine - pyrrolo[2,3-d]pyrimidine- ribonucleoside synthesis
    • Seela, F.; Peng, X. Progress in 7-deazapurine - pyrrolo[2,3-d]pyrimidine- ribonucleoside synthesis. Curr. Top. Med. Chem., 2006, 6, 867-892.
    • (2006) Curr. Top. Med. Chem. , vol.6 , pp. 867-892
    • Seela, F.1    Peng, X.2
  • 32
    • 0026387906 scopus 로고
    • Current progress on nucleoside antibiotics
    • Isono, K. Current progress on nucleoside antibiotics. Pharmacol. Ther., 1991, 52(3), 269-286.
    • (1991) Pharmacol. Ther. , vol.52 , Issue.3 , pp. 269-286
    • Isono, K.1
  • 33
    • 0001684125 scopus 로고
    • Synthesis of 2-amino-7-(2'-deoxy-β-D-erythropentofuranosyl)-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one, a new isostere of 2'-deoxyguanosine
    • Winkeler, H.-D.; Seela, F. Synthesis of 2-amino-7-(2'-deoxy-β-D-erythropentofuranosyl)-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one, a new isostere of 2'-deoxyguanosine. J. Org. Chem., 1983, 48(18), 3119-3122.
    • (1983) J. Org. Chem. , vol.48 , Issue.18 , pp. 3119-3122
    • Winkeler, H.-D.1    Seela, F.2
  • 34
    • 37049080632 scopus 로고
    • Liquid-liquid and solid-liquid phasetransfer glycosylation of pyrrolo[2,3-d]pyrimidines: Stereospecific synthesis of 2-deoxy-β-D-ribofuranosides related to 2'-deoxy-7-carbaguanosine
    • Seela, F.; Westermann, B.; Bindig, U. Liquid-liquid and solid-liquid phasetransfer glycosylation of pyrrolo[2,3-d]pyrimidines: stereospecific synthesis of 2-deoxy-β-D-ribofuranosides related to 2'-deoxy-7-carbaguanosine. J. Chem. Soc., Perkin Trans. 1, 1988, 697-702.
    • (1988) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 697-702
    • Seela, F.1    Westermann, B.2    Bindig, U.3
  • 35
    • 0017749199 scopus 로고
    • Synthesis of 5-methyltubercidin and its α-anomer via condensation of the anion of 4-methoxy-5-methyl-2-methylthiopyrrolo[2,3-d]pyrimidine and 2,3,5-Tri-O-benzyl-D-ribofuranosyl Bromide
    • Kondo, T.; Ohgi, T.; Goto, T. Synthesis of 5-methyltubercidin and its α-anomer via condensation of the anion of 4-methoxy-5-methyl-2-methylthiopyrrolo[2,3-d]pyrimidine and 2,3,5-Tri-O-benzyl-D-ribofuranosyl Bromide. Agric. Biol. Chem., 1977, 41(8), 1501-1507.
    • (1977) Agric. Biol. Chem. , vol.41 , Issue.8 , pp. 1501-1507
    • Kondo, T.1    Ohgi, T.2    Goto, T.3
  • 36
    • 0344915276 scopus 로고
    • Total synthesis of nucleoside Q
    • Ohgi, T.; Kondo, T.; Goto, T. Total synthesis of nucleoside Q. Tetrahedron Lett., 1977, 18(46), 4051-4054.
    • (1977) Tetrahedron Lett , vol.18 , Issue.46 , pp. 4051-4054
    • Ohgi, T.1    Kondo, T.2    Goto, T.3
  • 37
    • 0018677025 scopus 로고
    • 7-(β-D-Arabinofuranosyl)pyrrolo[2,3-d]pyrimidin-4(3H)-on - das 7-desazaderivat des antiviralen Nucleosids Ara-H
    • Lüpke, U.; Seela, F. 7-(β-D-Arabinofuranosyl)pyrrolo[2,3-d]pyrimidin-4(3H)-on - das 7-desazaderivat des antiviralen Nucleosids Ara-H. Chem. Ber., 1979, 112(10), 3432-3440.
    • (1979) Chem. Ber. , vol.112 , Issue.10 , pp. 3432-3440
    • Lüpke, U.1    Seela, F.2
  • 38
    • 33845470620 scopus 로고
    • Synthesis of 2'-deoxytubercidin, 2'-deoxyadenosine, and related 2'-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure
    • Kazimierczuk, Z.; Cottam, H. B.; Revankar, G. R.; Robins, R. K. Synthesis of 2'-deoxytubercidin, 2'-deoxyadenosine, and related 2'-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure. J. Am. Chem. Soc., 1984, 106(21), 6379-6382.
    • (1984) J. Am. Chem. Soc. , vol.106 , Issue.21 , pp. 6379-6382
    • Kazimierczuk, Z.1    Cottam, H.B.2    Revankar, G.R.3    Robins, R.K.4
  • 39
    • 0022372078 scopus 로고
    • Synthesis and biological activity of certain 6-substituted and 2,6-disubstituted 2'-deoxytubercidins prepared via the stereospecific sodium salt glycosylation procedure
    • Cottam, H. B.; Kazimierczuk, Z.; Geary, S.; McKernan, P. A.; Revankar, G. R.; Robins, R. K. Synthesis and biological activity of certain 6-substituted and 2,6-disubstituted 2'-deoxytubercidins prepared via the stereospecific sodium salt glycosylation procedure. J. Med. Chem., 1985, 28(10), 1461-1467.
    • (1985) J. Med. Chem. , vol.28 , Issue.10 , pp. 1461-1467
    • Cottam, H.B.1    Kazimierczuk, Z.2    Geary, S.3    McKernan, P.A.4    Revankar, G.R.5    Robins, R.K.6
  • 41
    • 84981759555 scopus 로고
    • α-Thymidin
    • Hoffer, M. α-Thymidin. Chem. Ber., 1960, 93(12), 2777-2781.
    • (1960) Chem. Ber. , vol.93 , Issue.12 , pp. 2777-2781
    • Hoffer, M.1
  • 42
    • 0010394312 scopus 로고
    • Nucleic acids components and their analogues. LIII. Preparation of 1-2'-deoxy-β-L-ribofuranosylthymine, L-thymine
    • Šmejkal, J.; Šorm, F. Nucleic acids components and their analogues. LIII. Preparation of 1-2'-deoxy-β-L-ribofuranosylthymine, L-thymine. Collect. Czech. Chem. Commun., 1964, 29, 2809-2813.
    • (1964) Collect. Czech. Chem. Commun. , vol.29 , pp. 2809-2813
    • Šmejkal, J.1    Šorm, F.2
  • 43
    • 84985209642 scopus 로고
    • Synthese von α-7-Desazaguanosin und Einfluß der Basenkonzentration auf die Phasentransferglycosylierung
    • Seela, F.; Hasselmann, D.; Winkeler, H.-D. Synthese von α-7-Desazaguanosin und Einfluß der Basenkonzentration auf die Phasentransferglycosylierung. Liebigs Ann. Chem., 1982, 499-506.
    • (1982) Liebigs Ann. Chem. , pp. 499-506
    • Seela, F.1    Hasselmann, D.2    Winkeler, H.-D.3
  • 44
    • 0020409315 scopus 로고
    • Synthese des α-Anomeren von ara-7-Desazaguanosin durch Phasentransferglycosylierung - Steuerung des Anomerenverhältnisses durch das quartäre Ammoniumsalz
    • Seela, F.; Winkeler, H.-D. Synthese des α-Anomeren von ara-7-Desazaguanosin durch Phasentransferglycosylierung - Steuerung des Anomerenverhältnisses durch das quartäre Ammoniumsalz. Liebigs Ann. Chem., 1982, 1634-1642.
    • (1982) Liebigs Ann. Chem. , pp. 1634-1642
    • Seela, F.1    Winkeler, H.-D.2
  • 45
    • 84985234168 scopus 로고
    • Synthese von Acyclo-7-desazaguanosin durch regiospezifische Phasentransferalkylierung von 2-Amino-4-methoxy-7H-pyrrolo-[2,3-d]pyrimidin
    • Seela, F.; Kehne, A.; Winkeler, H.-D. Synthese von Acyclo-7-desazaguanosin durch regiospezifische Phasentransferalkylierung von 2-Amino-4-methoxy-7H-pyrrolo-[2,3-d]pyrimidin. Liebigs Ann. Chem., 1983, 137-146.
    • (1983) Liebigs Ann. Chem. , pp. 137-146
    • Seela, F.1    Kehne, A.2    Winkeler, H.-D.3
  • 46
    • 85066848655 scopus 로고
    • Selective dealkylation of activated aromatic ethers
    • Hansson, C.; Wickberg, B. Selective dealkylation of activated aromatic ethers. Synthesis, 1976, 191-192.
    • (1976) Synthesis , pp. 191-192
    • Hansson, C.1    Wickberg, B.2
  • 47
    • 84985217574 scopus 로고
    • Synthese und Furanosid/Pyranosid-Isomerisierung von 7-Desaza-2'-desoxy-7-methylguanosin
    • Winkeler, H.-D.; Seela, F. Synthese und Furanosid/Pyranosid-Isomerisierung von 7-Desaza-2'-desoxy-7-methylguanosin. Liebigs Ann. Chem., 1984, 708-721.
    • (1984) Liebigs Ann. Chem. , pp. 708-721
    • Winkeler, H.-D.1    Seela, F.2
  • 48
    • 0020506272 scopus 로고
    • 2'-Desoxytubercidin - Synthese eines 2'-Desoxyadenosin-Isosteren durch Phasentransferglycosylierung
    • Seela, F.; Kehne, A. 2'-Desoxytubercidin - Synthese eines 2'-Desoxyadenosin-Isosteren durch Phasentransferglycosylierung. Liebigs Ann. Chem., 1983, 876-884.
    • (1983) Liebigs Ann. Chem. , pp. 876-884
    • Seela, F.1    Kehne, A.2
  • 49
    • 84985209632 scopus 로고
    • Synthese von 7-Desaza-2'-desoxyinosin durch Phasentransferglycosylierung
    • Seela, F.; Menkhoff, S. Synthese von 7-Desaza-2'-desoxyinosin durch Phasentransferglycosylierung. Liebigs Ann. Chem., 1985, 1360-1366.
    • (1985) Liebigs Ann. Chem. , pp. 1360-1366
    • Seela, F.1    Menkhoff, S.2
  • 50
    • 37049060811 scopus 로고
    • Pyrrolo[2,3-d]pyrimidines
    • Davoll, J. Pyrrolo[2,3-d]pyrimidines. J. Chem. Soc., 1960, 131-138.
    • (1960) J. Chem. Soc. , pp. 131-138
    • Davoll, J.1
  • 51
    • 84985279169 scopus 로고
    • Synthese von 2'-Desoxyribofuranosiden des 7H-Pyrrolo [2,3-d]pyrimidins: Einfluß des C-2-Substituenten auf die Fluoreszenz
    • Seela, F.; Steker, H. Synthese von 2'-Desoxyribofuranosiden des 7H-Pyrrolo [2,3-d]pyrimidins: Einfluß des C-2-Substituenten auf die Fluoreszenz. Liebigs Ann. Chem., 1984, 1719-1730.
    • (1984) Liebigs Ann. Chem. , pp. 1719-1730
    • Seela, F.1    Steker, H.2
  • 52
    • 84985200471 scopus 로고
    • Ara-7-Desazanebularin - Synthese eines fluoreszierenden Pyrrolo[2,3-d]pyrimidin-Nucleosids durch Phasentransferglycosylierung
    • Seela, F.; Steker, H. Ara-7-Desazanebularin - Synthese eines fluoreszierenden Pyrrolo[2,3-d]pyrimidin-Nucleosids durch Phasentransferglycosylierung. Liebigs Ann. Chem., 1983, 1576-1587.
    • (1983) Liebigs Ann. Chem. , pp. 1576-1587
    • Seela, F.1    Steker, H.2
  • 53
    • 84985279238 scopus 로고
    • 2-Amino-2'-desoxytubercidin und verwandte Pyrrolo[2,3-d]pyrimidinyl-2'-desoxyribofuranoside
    • Seela, F.; Steker, H.; Driller, H.; Bindig, U. 2-Amino-2'-desoxytubercidin und verwandte Pyrrolo[2,3-d]pyrimidinyl-2'-desoxyribofuranoside. Liebigs Ann. Chem., 1987, 15-19.
    • (1987) Liebigs Ann. Chem. , pp. 15-19
    • Seela, F.1    Steker, H.2    Driller, H.3    Bindig, U.4
  • 54
    • 0018821381 scopus 로고
    • 4-Amino-7-(β-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidin -die Synthese von Ara-Tubercidin durch Phasentransferkatalyse
    • Winkeler, H.-D.; Seela, F. 4-Amino-7-(β-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidin -die Synthese von Ara-Tubercidin durch Phasentransferkatalyse. Chem. Ber., 1980, 113(6), 2069-2080.
    • (1980) Chem. Ber. , vol.113 , Issue.6 , pp. 2069-2080
    • Winkeler, H.-D.1    Seela, F.2
  • 55
    • 0034040829 scopus 로고    scopus 로고
    • Synthesis, base pairing, and fluorescence properties of oligonucleotides containing 1H-Pyrazolo[3,4-d]pyrimidin-6-amine (8-aza-7-deazapurin-2-amine) as an analogue of purin-2-amine
    • Seela, F.; Becher, G. Synthesis, base pairing, and fluorescence properties of oligonucleotides containing 1H-Pyrazolo[3,4-d]pyrimidin-6-amine (8-aza-7-deazapurin-2-amine) as an analogue of purin-2-amine. Helv. Chim. Acta, 2000, 83(5), 928-942.
    • (2000) Helv. Chim. Acta. , vol.83 , Issue.5 , pp. 928-942
    • Seela, F.1    Becher, G.2
  • 56
    • 79955039237 scopus 로고    scopus 로고
    • DNA gold nanoparticle conjugates incorporating thiooxonucleosides: 7-deaza-6-thio-2'-deoxyguanosine as gold surface anchor
    • in press
    • Seela, F.; Ding, P.; Budow, S. DNA gold nanoparticle conjugates incorporating thiooxonucleosides: 7-deaza-6-thio-2'-deoxyguanosine as gold surface anchor. Bioconjugate Chem., 2011, in press.
    • (2011) Bioconjugate Chem
    • Seela, F.1    Ding, P.2    Budow, S.3
  • 57
    • 84985216519 scopus 로고
    • 4,4'-Dimethoxy-2,2'-bis(methylthio)-7,7'-methylendi(7H-pyrrolo[2,3-d]pyrimidin) - Phasentransferkatalysierte Aglyconverbrückung in Dichlormethan
    • Seela, F.; Menkhoff, S. 4,4'-Dimethoxy-2,2'-bis(methylthio)-7,7'-methylendi(7H-pyrrolo[2,3-d]pyrimidin) - Phasentransferkatalysierte Aglyconverbrückung in Dichlormethan. Liebigs Ann. Chem., 1982, 1405-1408.
    • (1982) Liebigs Ann. Chem. , pp. 1405-1408
    • Seela, F.1    Menkhoff, S.2
  • 58
    • 84985294444 scopus 로고
    • 7-(β-D-Arabinofuranosyl)-2,4-dichlor-7H-pyrrolo[2,3-d]pyrimidin- Synthese, selektiver Halogenaustausch und Einfluß glyconischer Schutzgruppen auf die Reaktivität des Aglycons
    • Seela, F.; Driller, H. 7-(β-D-Arabinofuranosyl)-2,4-dichlor-7H-pyrrolo[2,3-d]pyrimidin- Synthese, selektiver Halogenaustausch und Einfluß glyconischer Schutzgruppen auf die Reaktivität des Aglycons. Liebigs Ann. Chem., 1984, 722-733.
    • (1984) Liebigs Ann. Chem. , pp. 722-733
    • Seela, F.1    Driller, H.2
  • 59
    • 33845377169 scopus 로고
    • Tris(polyoxaalkyl)amines (trident), a new class of solid-liquid phase-transfer catalysts
    • Soula, G. Tris(polyoxaalkyl)amines (trident), a new class of solid-liquid phase-transfer catalysts. J. Org. Chem., 1985, 50(20), 3717-3721.
    • (1985) J. Org. Chem. , vol.50 , Issue.20 , pp. 3717-3721
    • Soula, G.1
  • 60
    • 25744476605 scopus 로고
    • Ribosidierung von 7H-Pyrrolo[2,3-d]pyrimidin-4(3H)-on an N-3
    • Lüpke, U.; Seela, F. Ribosidierung von 7H-Pyrrolo[2,3-d]pyrimidin-4(3H)-on an N-3. Chem. Ber., 1979, 112(10), 3526-3529.
    • (1979) Chem. Ber. , vol.112 , Issue.10 , pp. 3526-3529
    • Lüpke, U.1    Seela, F.2
  • 61
    • 0023726981 scopus 로고
    • Synthesis of 6-substituted 7-carbapurine 2',3'-dideoxynucleosides: Solid-liquid phase-transfer glycosylation of 4-chloropyrrolo[2,3-d]pyrimidine and deoxygenation of its 2'-deoxyribofuranoside
    • Seela, F.; Muth, H.-P.; Bindig, U. Synthesis of 6-substituted 7-carbapurine 2',3'-dideoxynucleosides: solid-liquid phase-transfer glycosylation of 4-chloropyrrolo[2,3-d]pyrimidine and deoxygenation of its 2'-deoxyribofuranoside. Synthesis, 1988, 670-674.
    • (1988) Synthesis , pp. 670-674
    • Seela, F.1    Muth, H.-P.2    Bindig, U.3
  • 62
    • 0024535636 scopus 로고
    • 2-formylation via a formamidine, phosphoramidite synthesis and properties of oligonucleotides
    • Seela, F.; Driller, H. 7-Deaza-2'-deoxy-O6-methylguanosine: selective N2-formylation via a formamidine, phosphoramidite synthesis and properties of oligonucleotides. Nucleosides Nucleotides, 1989, 8(1), 1-21.
    • (1989) Nucleosides Nucleotides , vol.8 , Issue.1 , pp. 1-21
    • Seela, F.1    Driller, H.2
  • 63
    • 0029135121 scopus 로고
    • 7-Substituted 7-deaza-2'-deoxyguanosines: Regioselective halogenation of pyrrolo[2,3-d]pyrimidine nucleosides
    • Ramzaeva, N.; Seela, F. 7-Substituted 7-deaza-2'-deoxyguanosines: regioselective halogenation of pyrrolo[2,3-d]pyrimidine nucleosides. Helv. Chim. Acta, 1995, 78(5), 1083-1090.
    • (1995) Helv. Chim. Acta. , vol.78 , Issue.5 , pp. 1083-1090
    • Ramzaeva, N.1    Seela, F.2
  • 64
    • 3142734409 scopus 로고    scopus 로고
    • 7-Halogenated 7-deaza-2'-deoxyxanthine 2'-deoxyribonucleosides
    • Seela, F.; Shaikh, K. 7-Halogenated 7-deaza-2'-deoxyxanthine 2'-deoxyribonucleosides. Helv. Chim. Acta, 2004, 87(6), 1325-1332.
    • (2004) Helv. Chim. Acta. , vol.87 , Issue.6 , pp. 1325-1332
    • Seela, F.1    Shaikh, K.2
  • 65
    • 0031708492 scopus 로고    scopus 로고
    • Facile synthesis of 2'-deoxynucleoside analogs of preQ
    • Ramzaeva, N.; Becher, G.; Seela, F. Facile synthesis of 2'-deoxynucleoside analogs of preQ. Synthesis, 1998, 1327-1330.
    • (1998) Synthesis , pp. 1327-1330
    • Ramzaeva, N.1    Becher, G.2    Seela, F.3
  • 66
    • 78449278501 scopus 로고    scopus 로고
    • 0, 7-cyano-7-deazaguanosine, via microwave-assisted iodo → carbonitrile exchange
    • Ming, X.; Seela, F. Efficient synthesis of the tRNA nucleoside preQ0, 7-cyano-7-deazaguanosine, via microwave-assisted iodo → carbonitrile exchange. Chem. Biodivers., 2010, 7, 2616-2621.
    • (2010) Chem. Biodivers. , vol.7 , pp. 2616-2621
    • Ming, X.1    Seela, F.2
  • 67
    • 33745741145 scopus 로고    scopus 로고
    • Fluorinated pyrrolo[2,3-d]pyrimidine nucleosides: 7-fluoro-7-deazapurine 2'-deoxyribofuranosides and 2'-deoxy-2'-fluoroarabinofuranosyl derivatives
    • Seela, F.; Xu, K.; Chittepu, P. Fluorinated pyrrolo[2,3-d]pyrimidine nucleosides: 7-fluoro-7-deazapurine 2'-deoxyribofuranosides and 2'-deoxy-2'-fluoroarabinofuranosyl derivatives. Synthesis, 2006, 2005-2012.
    • (2006) Synthesis , pp. 2005-2012
    • Seela, F.1    Xu, K.2    Chittepu, P.3
  • 68
    • 26644465100 scopus 로고    scopus 로고
    • 6-Azapyrimidine and 7-deazapurine 2'-deoxy-2'-fluoroarabinonucleosides: Synthesis, conformation and properties of oligonucleotides
    • Seela, F.; Chittepu, P.; He, Y.; He, J.; Xu, K. 6-Azapyrimidine and 7-deazapurine 2'-deoxy-2'-fluoroarabinonucleosides: synthesis, conformation and properties of oligonucleotides. Nucleosides Nucleotides Nucleic Acids, 2005, 24(5), 847-850.
    • (2005) Nucleosides Nucleotides Nucleic Acids , vol.24 , Issue.5 , pp. 847-850
    • Seela, F.1    Chittepu, P.2    He, Y.3    He, J.4    Xu, K.5
  • 69
    • 36949006078 scopus 로고    scopus 로고
    • Fluorinated 7-deazapurine 2'-deoxyribonucleosides: Modification at the nucleobase and the sugar moiety
    • Seela, F.; Xu, K.; Chittepu, P.; Ming, X. Fluorinated 7-deazapurine 2'-deoxyribonucleosides: modification at the nucleobase and the sugar moiety. Nucleosides Nucleotides Nucleic Acids, 2007, 26(6), 607-610.
    • (2007) Nucleosides Nucleotides Nucleic Acids , vol.26 , Issue.6 , pp. 607-610
    • Seela, F.1    Xu, K.2    Chittepu, P.3    Ming, X.4
  • 70
    • 2942711907 scopus 로고    scopus 로고
    • Regioselective syntheses of 7-halogenated 7-deazapurine nucleosides related to 2-amino-7-deaza-2'-deoxyadenosine and 7-deaza-2'-deoxyisoguanosine
    • Seela, F.; Peng, X. Regioselective syntheses of 7-halogenated 7-deazapurine nucleosides related to 2-amino-7-deaza-2'-deoxyadenosine and 7-deaza-2'-deoxyisoguanosine. Synthesis, 2004, 1203-1210.
    • (2004) Synthesis , pp. 1203-1210
    • Seela, F.1    Peng, X.2
  • 71
    • 0030809054 scopus 로고    scopus 로고
    • Methylated DNA: The influence of 7-deaza-7-methylguanine on the structure and stability of oligonucleotides
    • Seela, F.; Chen, Y. Methylated DNA: the influence of 7-deaza-7-methylguanine on the structure and stability of oligonucleotides. Helv. Chim. Acta, 1997, 80(4), 1073-1086.
    • (1997) Helv. Chim. Acta. , vol.80 , Issue.4 , pp. 1073-1086
    • Seela, F.1    Chen, Y.2
  • 72
    • 0025314762 scopus 로고
    • Synthesis, antiproliferative, and antiviral activity of certain 4-substituted and 4,5-disubstituted 7-[(1,3-dihydroxy-2-propoxy)methyl]pyrrolo[2,3-d]pyrimidines
    • Pudlo, J. S.; Nassiri, M. R.; Kern, E. R.; Wotring, L. L.; Drach, J. C.; Townsend, L. B. Synthesis, antiproliferative, and antiviral activity of certain 4-substituted and 4,5-disubstituted 7-[(1,3-dihydroxy-2-propoxy)methyl]pyrrolo[2,3-d]pyrimidines. J. Med. Chem., 1990, 33(7), 1984-1992.
    • (1990) J. Med. Chem. , vol.33 , Issue.7 , pp. 1984-1992
    • Pudlo, J.S.1    Nassiri, M.R.2    Kern, E.R.3    Wotring, L.L.4    Drach, J.C.5    Townsend, L.B.6
  • 74
    • 0028285871 scopus 로고
    • Synthesis of certain 5-substituted 2'-deoxytubercidin derivatives
    • Seela, F.; Thomas, H. Synthesis of certain 5-substituted 2'-deoxytubercidin derivatives. Helv. Chim. Acta, 1994, 77(4), 897-903.
    • (1994) Helv. Chim. Acta. , vol.77 , Issue.4 , pp. 897-903
    • Seela, F.1    Thomas, H.2
  • 75
    • 0029844007 scopus 로고    scopus 로고
    • Palladium-catalyzed cross coupling of 7-iodo-2'-deoxytubercidin with terminal alkynes
    • Seela, F.; Zulauf, M. Palladium-catalyzed cross coupling of 7-iodo-2'-deoxytubercidin with terminal alkynes. Synthesis, 1996, 726-730.
    • (1996) Synthesis , pp. 726-730
    • Seela, F.1    Zulauf, M.2
  • 76
  • 77
    • 0347679707 scopus 로고    scopus 로고
    • 7-Nitro-7-deaza-2'-deoxyadenosine and 8-methyl-7-deaza-2'-deoxyguanosine: Pyrrolo[2,3-d]pyrimidine nucleosides with different sugar conformations
    • Seela, F.; Rosemeyer, H.; Zulauf, M.; Chen, Y.; Kastner, G.; Reuter, H. 7-Nitro-7-deaza-2'-deoxyadenosine and 8-methyl-7-deaza-2'-deoxyguanosine: pyrrolo[2,3-d]pyrimidine nucleosides with different sugar conformations. Liebigs Ann./Recueil, 1997, 2525-2530.
    • (1997) Liebigs Ann./Recueil , pp. 2525-2530
    • Seela, F.1    Rosemeyer, H.2    Zulauf, M.3    Chen, Y.4    Kastner, G.5    Reuter, H.6
  • 78
    • 24944550539 scopus 로고    scopus 로고
    • Regioselective syntheses of 7-nitro-7-deazapurine nucleosides and nucleotides for efficient PCR incorporation
    • Kawate, T.; Allerson, C. R.; Wolfe, J. L. Regioselective syntheses of 7-nitro-7-deazapurine nucleosides and nucleotides for efficient PCR incorporation. Org. Lett., 2005, 7(18), 3865-3868.
    • (2005) Org. Lett. , vol.7 , Issue.18 , pp. 3865-3868
    • Kawate, T.1    Allerson, C.R.2    Wolfe, J.L.3
  • 79
    • 33750076355 scopus 로고    scopus 로고
    • Synthesis and application of nitro-substituted nucleosides and nucleotides
    • Kawate, T.; Wang, B. H.; Allerson, C. R.; Wolfe, J. L. Synthesis and application of nitro-substituted nucleosides and nucleotides. Synthesis, 2006, 3280-3290.
    • (2006) Synthesis , pp. 3280-3290
    • Kawate, T.1    Wang, B.H.2    Allerson, C.R.3    Wolfe, J.L.4
  • 81
    • 0030062222 scopus 로고    scopus 로고
    • Template-directed interference footprinting of protein-adenine contacts
    • Min, C.; Cushing, T. D.; Verdine, G. L. Template-directed interference footprinting of protein-adenine contacts. J. Am. Chem. Soc., 1996, 118(26), 6116-6120.
    • (1996) J. Am. Chem. Soc. , vol.18 , Issue.26 , pp. 116-6120
    • Min, C.1    Cushing, T.D.2    Verdine, G.L.3
  • 82
    • 33947210076 scopus 로고    scopus 로고
    • 6-Etheno-2'-deoxytubercidin and pyrrolo-C: Synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides
    • Seela, F.; Schweinberger, E.; Xu, K.; Sirivolu, V. R.; Rosemeyer, H.; Becker, E.-M. 1,N6-Etheno-2'-deoxytubercidin and pyrrolo-C: synthesis, base pairing, and fluorescence properties of 7-deazapurine nucleosides and oligonucleotides. Tetrahedron, 2007, 63(17), 3471-3482.
    • (2007) Tetrahedron , vol.63 , Issue.17 , pp. 3471-3482
    • Seela, F.1    Schweinberger, E.2    Xu, K.3    Sirivolu, V.R.4    Rosemeyer, H.5    Becker, E.-M.6
  • 83
    • 33845659916 scopus 로고    scopus 로고
    • pH-Dependent mismatch discrimination of oligonucleotide duplexes containing 2'-deoxytubercidin and 2- or 7-substituted derivatives: Protonated base pairs formed between 7-deazapurines and cytosine
    • Peng, X.; Li, H.; Seela, F. pH-Dependent mismatch discrimination of oligonucleotide duplexes containing 2'-deoxytubercidin and 2- or 7-substituted derivatives: protonated base pairs formed between 7-deazapurines and cytosine. Nucleic Acids Res., 2006, 34(20), 5987-6000.
    • (2006) Nucleic Acids Res , vol.34 , Issue.20 , pp. 5987-6000
    • Peng, X.1    Li, H.2    Seela, F.3
  • 84
    • 52149111758 scopus 로고    scopus 로고
    • 7-Halogenated 7-deazapurine 2'-deoxyribonucleosides related to 2'-deoxyadenosine, 2'-deoxyxanthosine, and 2'-deoxyisoguanosine: Syntheses and properties
    • Seela, F.; Xu, K. 7-Halogenated 7-deazapurine 2'-deoxyribonucleosides related to 2'-deoxyadenosine, 2'-deoxyxanthosine, and 2'-deoxyisoguanosine: syntheses and properties. Helv. Chim. Acta, 2008, 91(6), 1083-1105.
    • (2008) Helv. Chim. Acta. , vol.91 , Issue.6 , pp. 1083-1105
    • Seela, F.1    Xu, K.2
  • 85
    • 84987487263 scopus 로고
    • 2'-Deoxyisoguanosine and base-modified analogues: Chemical and photochemical synthesis
    • Kazimierczuk, Z.; Mertens, R.; Kawczynski, W.; Seela, F. 2'-Deoxyisoguanosine and base-modified analogues: chemical and photochemical synthesis. Helv. Chim. Acta, 1991, 74(8), 1742-1748.
    • (1991) Helv. Chim. Acta. , vol.74 , Issue.8 , pp. 1742-1748
    • Kazimierczuk, Z.1    Mertens, R.2    Kawczynski, W.3    Seela, F.4
  • 86
    • 0032894327 scopus 로고    scopus 로고
    • The base-pairing properties of 7-deaza-2'- deoxyisoguanosine and 2'-deoxyisoguanosine in oligonucleotide duplexes with parallel and antiparallel chain orientation
    • Seela, F.; Wei, C. The base-pairing properties of 7-deaza-2'- deoxyisoguanosine and 2'-deoxyisoguanosine in oligonucleotide duplexes with parallel and antiparallel chain orientation. Helv. Chim. Acta, 1999, 82(5), 726-745.
    • (1999) Helv. Chim. Acta. , vol.82 , Issue.5 , pp. 726-745
    • Seela, F.1    Wei, C.2
  • 87
    • 0032528042 scopus 로고    scopus 로고
    • Biophysical and antisense properties of oligodeoxynucleotides containing 7-propynyl-, 7-iodo- and 7-cyano-7-deaza-2-amino-2'-deoxyadenosines
    • Balow, G.; Mohan, V.; Lesnik, E. A.; Johnston, J. F.; Monia, B. P.; Acevedo, O. L. Biophysical and antisense properties of oligodeoxynucleotides containing 7-propynyl-, 7-iodo- and 7-cyano-7-deaza-2-amino-2'-deoxyadenosines. Nucleic Acids Res., 1998, 26(14), 3350-3357.
    • (1998) Nucleic Acids Res , vol.26 , Issue.14 , pp. 3350-3357
    • Balow, G.1    Mohan, V.2    Lesnik, E.A.3    Johnston, J.F.4    Monia, B.P.5    Acevedo, O.L.6
  • 89
    • 0017198622 scopus 로고
    • Tautomerism of isoguanosine and solvent-induced keto-enol equilibrium
    • Sepiol, J.; Kazimierczuk, Z.; Shugar, D. Tautomerism of isoguanosine and solvent-induced keto-enol equilibrium. Z. Naturforsch., C: Biosci., 1976, 31(7-8), 361-370.
    • (1976) Z. Naturforsch., C: Biosci. , vol.31 , Issue.7-8 , pp. 361-370
    • Sepiol, J.1    Kazimierczuk, Z.2    Shugar, D.3
  • 90
    • 0032483053 scopus 로고    scopus 로고
    • 2'-Deoxyisoguanosine adopts more than one tautomer to form base pairs with thymidine observed by high-resolution crystal structure analysis
    • Robinson, H.; Gao, Y.-G.; Bauer, C.; Roberts, C.; Switzer, C.; Wang, A. H.-J. 2'-Deoxyisoguanosine adopts more than one tautomer to form base pairs with thymidine observed by high-resolution crystal structure analysis. Biochemistry, 1998, 37(31), 10897-10905.
    • (1998) Biochemistry , vol.37 , Issue.31 , pp. 10897-10905
    • Robinson, H.1    Gao, Y.-G.2    Bauer, C.3    Roberts, C.4    Switzer, C.5    Wang, A.H.-J.6
  • 91
    • 0024325247 scopus 로고
    • Enzymatic incorporation of a new base pair into DNA and RNA
    • Switzer, C.; Moroney, S. E.; Benner, S. A. Enzymatic incorporation of a new base pair into DNA and RNA. J. Am. Chem. Soc., 1989, 111(21), 8322-8323.
    • (1989) J. Am. Chem. Soc. , vol.111 , Issue.21 , pp. 8322-8323
    • Switzer, C.1    Moroney, S.E.2    Benner, S.A.3
  • 92
    • 2442675347 scopus 로고    scopus 로고
    • Artificial genetic systems: Exploiting the "aromaticity" formalism to improve the tautomeric ratio for isoguanosine derivatives
    • Martinot, T. A.; Benner, S. A. Artificial genetic systems: exploiting the "aromaticity" formalism to improve the tautomeric ratio for isoguanosine derivatives. J. Org. Chem., 2004, 69(11), 3972-3975.
    • (2004) J. Org. Chem. , vol.69 , Issue.11 , pp. 3972-3975
    • Martinot, T.A.1    Benner, S.A.2
  • 93
    • 19744374519 scopus 로고    scopus 로고
    • Base-pairing, tautomerism, and mismatch discrimination of 7-halogenated 7-deaza-2'-deoxyisoguanosine: Oligonucleotide duplexes with parallel and antiparallel chain orientation
    • Seela, F.; Peng, X.; Li, H. Base-pairing, tautomerism, and mismatch discrimination of 7-halogenated 7-deaza-2'-deoxyisoguanosine: oligonucleotide duplexes with parallel and antiparallel chain orientation. J. Am. Chem. Soc., 2005, 127(21), 7739-7751.
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.21 , pp. 7739-7751
    • Seela, F.1    Peng, X.2    Li, H.3
  • 95
    • 0031913678 scopus 로고    scopus 로고
    • Synthesis of 2',3'-didehydro-2',3'-dideoxyisoinosine and oxidation of fluorescent 2-hydroxypurine nucleosides by xanthine oxidase
    • Seela, F.; Chen, Y.; Sauer, M. Synthesis of 2',3'-didehydro-2',3'-dideoxyisoinosine and oxidation of fluorescent 2-hydroxypurine nucleosides by xanthine oxidase. Nucleosides Nucleotides, 1998, 17(1), 39-52.
    • (1998) Nucleosides Nucleotides , vol.17 , Issue.1 , pp. 39-52
    • Seela, F.1    Chen, Y.2    Sauer, M.3
  • 96
    • 0021329689 scopus 로고
    • Ara-7-Desazaxanthosin - ein Xanthin-Nucleosid mit stabiler N-glycosylischer Bindung
    • Seela, F.; Liman, U. Ara-7-Desazaxanthosin - ein Xanthin-Nucleosid mit stabiler N-glycosylischer Bindung. Liebigs Ann. Chem., 1984, 273-282.
    • (1984) Liebigs Ann. Chem. , pp. 273-282
    • Seela, F.1    Liman, U.2
  • 97
    • 0028090742 scopus 로고
    • Synthesis of 2'-deoxyisoinosine and related 2'-deoxyribonucleosides
    • Seela, F.; Chen, Y.; Bindig, U.; Kazimierczuk, Z. Synthesis of 2'-deoxyisoinosine and related 2'-deoxyribonucleosides. Helv. Chim. Acta, 1994, 77(1), 194-202.
    • (1994) Helv. Chim. Acta. , vol.77 , Issue.1 , pp. 194-202
    • Seela, F.1    Chen, Y.2    Bindig, U.3    Kazimierczuk, Z.4
  • 98
    • 0034500810 scopus 로고    scopus 로고
    • Fluorescence properties and base pair stability of oligonucleotides containing 8-aza-7-deaza-2'-deoxyisoinosine or 2'-deoxyisoinosine
    • Seela, F.; Becher, G.; Chen, Y. Fluorescence properties and base pair stability of oligonucleotides containing 8-aza-7-deaza-2'-deoxyisoinosine or 2'-deoxyisoinosine. Nucleosides Nucleotides Nucleic Acids, 2000, 19(10), 1581-1598.
    • (2000) Nucleosides Nucleotides Nucleic Acids , vol.19 , Issue.10 , pp. 1581-1598
    • Seela, F.1    Becher, G.2    Chen, Y.3
  • 99
    • 33847697415 scopus 로고
    • Bevorzugte β-Glycosidbildung durch Phasentransfer-Katalyse bei der Synthese von D-Arabinofuranosyl-7-desazapurinnucleosiden
    • Seela, F.; Winkeler, D. Bevorzugte β-Glycosidbildung durch Phasentransfer-Katalyse bei der Synthese von D-Arabinofuranosyl-7-desazapurinnucleosiden. Angew. Chem., 1979, 91(7), 570-571.
    • (1979) Angew. Chem. , vol.91 , Issue.7 , pp. 570-571
    • Seela, F.1    Winkeler, D.2
  • 100
    • 0030035948 scopus 로고    scopus 로고
    • Oligodeoxynucleotides containing C-7 propyne analogs of 7-deaza-2'-deoxyguanosine and 7-deaza-2'-deoxyadenosine
    • Buhr, C. A.; Wagner, R. W.; Grant, D.; Froehler, B. C. Oligodeoxynucleotides containing C-7 propyne analogs of 7-deaza-2'-deoxyguanosine and 7-deaza-2'-deoxyadenosine. Nucleic Acids Res., 1996, 24(15), 2974-2980.
    • (1996) Nucleic Acids Res , vol.24 , Issue.15 , pp. 2974-2980
    • Buhr, C.A.1    Wagner, R.W.2    Grant, D.3    Froehler, B.C.4
  • 102
    • 0029117656 scopus 로고
    • A new synthetic route to β-2'-deoxyribosyl-5-substituted pyrrolo[2,3-d]pyrimidines. Synthesis of 2'-deoxycadeguomycin
    • Edstrom, E. D.; Wei, Y. A new synthetic route to β-2'-deoxyribosyl-5-substituted pyrrolo[2,3-d]pyrimidines. Synthesis of 2'-deoxycadeguomycin. J. Org. Chem., 1995, 60(16), 5069-5076.
    • (1995) J. Org. Chem. , vol.60 , Issue.16 , pp. 5069-5076
    • Edstrom, E.D.1    Wei, Y.2
  • 103
    • 0024206813 scopus 로고
    • A Facile and improved synthesis of tubercidin and certain related pyrrolo[2,3-d]pyrimidine nucleosides by the stereospecific sodium salt glycosylation procedure
    • Ramasamy, K.; Imamura, N.; Robins, R. K.; Revankar, G. R. A Facile and improved synthesis of tubercidin and certain related pyrrolo[2,3-d]pyrimidine nucleosides by the stereospecific sodium salt glycosylation procedure. J. Heterocycl. Chem., 1988, 25, 1893-1898.
    • (1988) J. Heterocycl. Chem. , vol.25 , pp. 1893-1898
    • Ramasamy, K.1    Imamura, N.2    Robins, R.K.3    Revankar, G.R.4
  • 104
    • 0024327312 scopus 로고
    • Use of the sodium salt glycosylation in nucleoside synthesis
    • Revankar, G. R.; Robins, R. K. Use of the sodium salt glycosylation in nucleoside synthesis. Nucleosides Nucleotides, 1989, 8(5), 709-724.
    • (1989) Nucleosides Nucleotides , vol.8 , Issue.5 , pp. 709-724
    • Revankar, G.R.1    Robins, R.K.2
  • 105
    • 0023584307 scopus 로고
    • A facile synthesis of tubercidin and related 7-deazapurine nucleosides via the stereospecific sodium salt glycosylation procedure
    • Ramasamy, K.; Imamura, N.; Robins, R. K.; Revankar, G. R. A facile synthesis of tubercidin and related 7-deazapurine nucleosides via the stereospecific sodium salt glycosylation procedure. Tetrahedron Lett., 1987, 28(43), 5107-5110.
    • (1987) Tetrahedron Lett , vol.28 , Issue.43 , pp. 5107-5110
    • Ramasamy, K.1    Imamura, N.2    Robins, R.K.3    Revankar, G.R.4
  • 106
    • 0023008821 scopus 로고
    • Total synthesis of 2'-deoxytoyocamycin, 2'-deoxysangivamycin and related 7-β-Darabinofuranosylpyrrolo[2,3-d]pyrimidines via ring closure of pyrrole precursors prepared by the stereospecific sodium salt glycosylation procedure
    • Ramasamy, K.; Robins, R. K.; Revankar, G. R. Total synthesis of 2'-deoxytoyocamycin, 2'-deoxysangivamycin and related 7-β-Darabinofuranosylpyrrolo[2,3-d]pyrimidines via ring closure of pyrrole precursors prepared by the stereospecific sodium salt glycosylation procedure. Tetrahedron, 1986, 42(21), 5869-5878.
    • (1986) Tetrahedron , vol.42 , Issue.21 , pp. 5869-5878
    • Ramasamy, K.1    Robins, R.K.2    Revankar, G.R.3
  • 107
    • 0002864205 scopus 로고
    • Aromaticity in heterocyclic systems. II. The application of N.M.R. in a study of the synthesis and structure of certain imidazo[1,2-c]pyrimidines and related pyrrolo[2,3-d]pyrimidines
    • Noell, C. W.; Robins, R. K. Aromaticity in heterocyclic systems. II. The application of N.M.R. in a study of the synthesis and structure of certain imidazo[1,2-c]pyrimidines and related pyrrolo[2,3-d]pyrimidines. J. Heterocycl. Chem., 1964, 1(1), 34-41.
    • (1964) J. Heterocycl. Chem. , vol.1 , Issue.1 , pp. 34-41
    • Noell, C.W.1    Robins, R.K.2
  • 108
    • 25044458867 scopus 로고
    • 7-Desaza-Isostere von 2'-Desoxyxanthosin und 2'-Desoxyspongosin - Synthese via Glycosylierung von 2,4-Dichlor-Hpyrrolo[2,3-d]pyrimidin
    • Seela, F.; Driller, H.; Liman, U. 7-Desaza-Isostere von 2'-Desoxyxanthosin und 2'-Desoxyspongosin - Synthese via Glycosylierung von 2,4-Dichlor-Hpyrrolo[2,3-d]pyrimidin. Liebigs Ann. Chem., 1985, 312-320.
    • (1985) Liebigs Ann. Chem. , pp. 312-320
    • Seela, F.1    Driller, H.2    Liman, U.3
  • 109
    • 0037084326 scopus 로고    scopus 로고
    • 7-Deaza-2'-deoxyxanthosine dihydrate forms water-filled nanotubes with C-H·O hydrogen bonds
    • Seela, F.; Wiglenda, T.; Rosemeyer, H.; Eickmeier, H.; Reuter, H. 7-Deaza-2'-deoxyxanthosine dihydrate forms water-filled nanotubes with C-H·O hydrogen bonds. Angew. Chem. Int. Ed., 2002, 41(4), 603-605.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , Issue.4 , pp. 603-605
    • Seela, F.1    Wiglenda, T.2    Rosemeyer, H.3    Eickmeier, H.4    Reuter, H.5
  • 110
    • 37049067246 scopus 로고
    • Total and stereospecific synthesis of cadeguomycin, 2'-deoxycadeguomycin, aracadeguomycin, and certain related nucleosides
    • Ramasamy, K.; Joshi, R. V.; Robins, R. K.; Revankar, G. R. Total and stereospecific synthesis of cadeguomycin, 2'-deoxycadeguomycin, aracadeguomycin, and certain related nucleosides. J. Chem. Soc., Perkin Trans. 1, 1989, 2375-2384.
    • (1989) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2375-2384
    • Ramasamy, K.1    Joshi, R.V.2    Robins, R.K.3    Revankar, G.R.4
  • 114
    • 37049103153 scopus 로고
    • Synthesis of 2'-deoxytubercidin {4-amino-7-(2-deoxy-β-D-erythro-pentofuranosyl)pyrrolo[2,3-d]pyrimidine} from the parent antibiotic
    • Robins, M. J.; Muhs, W. H. Synthesis of 2'-deoxytubercidin {4-amino-7-(2-deoxy-β-D-erythro-pentofuranosyl)pyrrolo[2,3-d]pyrimidine} from the parent antibiotic. J. Chem. Soc., Chem. Commun., 1976, 269-269.
    • (1976) J. Chem. Soc., Chem. Commun. , pp. 269
    • Robins, M.J.1    Muhs, W.H.2
  • 115
    • 0344902741 scopus 로고
    • A new method for the deoxygenation of secondary alcohols
    • Barton, D. H. R.; McCombie, S. W. A new method for the deoxygenation of secondary alcohols. J. Chem. Soc., Perkin Trans. 1, 1975, 1574-1585.
    • (1975) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1574-1585
    • Barton, D.H.R.1    McCombie, S.W.2
  • 116
    • 33845556029 scopus 로고
    • Smooth and efficient deoxygenation of secondary alcohols. A general procedure for the conversion of ribonucleosides to 2'-deoxynucleosides
    • Robins, M. J.; Wilson, J. S. Smooth and efficient deoxygenation of secondary alcohols. A general procedure for the conversion of ribonucleosides to 2'-deoxynucleosides. J. Am. Chem. Soc., 1981, 103(4), 932-933.
    • (1981) J. Am. Chem. Soc. , vol.103 , Issue.4 , pp. 932-933
    • Robins, M.J.1    Wilson, J.S.2
  • 117
    • 0020764119 scopus 로고
    • Nucleic acid related compounds. 42. A general procedure for the efficient deoxygenation of secondary alcohols. Regiospecific and stereoselective conversion of ribonucleosides to 2'-deoxynucleosides
    • Robins, M. J.; Wilson, J. S.; Hansske, F. Nucleic acid related compounds. 42. A general procedure for the efficient deoxygenation of secondary alcohols. Regiospecific and stereoselective conversion of ribonucleosides to 2'-deoxynucleosides. J. Am. Chem. Soc., 1983, 105(12), 4059-4065.
    • (1983) J. Am. Chem. Soc. , vol.105 , Issue.12 , pp. 4059-4065
    • Robins, M.J.1    Wilson, J.S.2    Hansske, F.3
  • 118
    • 0001378124 scopus 로고
    • The reaction of 1,3-dichloro-1,1,3,3-tetraisopropyldisiloxane with cytosine arabinoside and 1-(6-deoxy-β-L-talofuransyl)uracil
    • Markiewicz, W. T.; Payukova, N. S.; Samek, Z.; Smrt, J. J. The reaction of 1,3-dichloro-1,1,3,3-tetraisopropyldisiloxane with cytosine arabinoside and 1-(6-deoxy-β-L-talofuransyl)uracil. Collect. Czech. Chem. Commun., 1980, 45, 1860-1865.
    • (1980) Collect. Czech. Chem. Commun. , vol.45 , pp. 1860-1865
    • Markiewicz, W.T.1    Payukova, N.S.2    Samek, Z.3    Smrt, J.J.4
  • 119
    • 0347318701 scopus 로고
    • Reactions of 2-acyloxyisobutyryl halides with nucleosides. III. Reactions of tubercidin and formycin
    • Jain, T. C.; Russell, A. F.; Moffatt, J. G. Reactions of 2-acyloxyisobutyryl halides with nucleosides. III. Reactions of tubercidin and formycin. J. Org. Chem., 1973, 38(18), 3179-3186.
    • (1973) J. Org. Chem. , vol.38 , Issue.18 , pp. 3179-3186
    • Jain, T.C.1    Russell, A.F.2    Moffatt, J.G.3
  • 120
    • 0017333211 scopus 로고
    • Nucleic acid related compounds. 24. Transformation of tubercidin 2',3'-O-orthoacetate into halo, deoxy, epoxide, and unsaturated sugar nucleosides
    • Robins, M. J.; Jones, R. A.; Mengel, R. Nucleic acid related compounds. 24. Transformation of tubercidin 2',3'-O-orthoacetate into halo, deoxy, epoxide, and unsaturated sugar nucleosides. Can. J. Chem., 1977, 55(7), 1251-1259.
    • (1977) Can. J. Chem. , vol.55 , Issue.7 , pp. 1251-1259
    • Robins, M.J.1    Jones, R.A.2    Mengel, R.3
  • 121
    • 0024500466 scopus 로고
    • 2',3'-Dideoxyadenosine analogs of the nucleoside antibiotics tubercidin, toyocamycin and sangivamycin
    • Krawczyk, S. H.; Townsend, L. B. 2',3'-Dideoxyadenosine analogs of the nucleoside antibiotics tubercidin, toyocamycin and sangivamycin. Nucleosides Nucleotides, 1989, 8(1), 97-115.
    • (1989) Nucleosides Nucleotides , vol.8 , Issue.1 , pp. 97-115
    • Krawczyk, S.H.1    Townsend, L.B.2
  • 122
    • 0026328196 scopus 로고
    • Base-modified purine 2',3'-dideoxyribonucleosides: Synthesis via deoxygenation or direct nucleobase anion glycosylation
    • Seela, F.; Rosemeyer, H.; Gumbiowski, R.; Mersmann, K.; Muth, H.-P.; Röling, A. Base-modified purine 2',3'-dideoxyribonucleosides: synthesis via deoxygenation or direct nucleobase anion glycosylation. Nucleosides Nucleotides, 1991, 10(1), 409-412.
    • (1991) Nucleosides Nucleotides , vol.10 , Issue.1 , pp. 409-412
    • Seela, F.1    Rosemeyer, H.2    Gumbiowski, R.3    Mersmann, K.4    Muth, H.-P.5    Röling, A.6
  • 123
    • 0032560090 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship of ribofuranosyl echiguanine analogs as inhibitors of phosphatidylinositol 4-kinase
    • Saito, Y.; Kato, K.; Umezawa, K. Synthesis and structure-activity relationship of ribofuranosyl echiguanine analogs as inhibitors of phosphatidylinositol 4-kinase. Tetrahedron, 1998, 54(17), 4251-4266.
    • (1998) Tetrahedron , vol.54 , Issue.17 , pp. 4251-4266
    • Saito, Y.1    Kato, K.2    Umezawa, K.3
  • 124
    • 0031681373 scopus 로고    scopus 로고
    • 7-Deazaadenine-DNA: Bulky 7-iodo substituents or hydrophobic 7-hexynyl chains are well accommodated in the major groove of oligonucleotide duplexes
    • Seela, F.; Zulauf, M. 7-Deazaadenine-DNA: bulky 7-iodo substituents or hydrophobic 7-hexynyl chains are well accommodated in the major groove of oligonucleotide duplexes. Chem. Eur. J., 1998, 4(9), 1781-1790.
    • (1998) Chem. Eur. J. , vol.4 , Issue.9 , pp. 1781-1790
    • Seela, F.1    Zulauf, M.2
  • 125
    • 0034676686 scopus 로고    scopus 로고
    • Synthesis and duplex stability of oligonucleotides containing 7-vinyl-7-deazaguanine as a strong electrondonating nucleobase
    • Okamoto, A.; Taiji, T.; Tanaka, K.; Saito, I. Synthesis and duplex stability of oligonucleotides containing 7-vinyl-7-deazaguanine as a strong electrondonating nucleobase. Tetrahedron Lett., 2000, 41(51), 10035-10039.
    • (2000) Tetrahedron Lett , vol.41 , Issue.51 , pp. 10035-10039
    • Okamoto, A.1    Taiji, T.2    Tanaka, K.3    Saito, I.4
  • 126
    • 8144224735 scopus 로고    scopus 로고
    • An analogue of adenine that forms an A:T base pair of comparable stability to G:C
    • Booth, J.; Cummins, W. J.; Brown, T. An analogue of adenine that forms an A:T base pair of comparable stability to G:C. Chem. Commun., 2004, 2208-2209.
    • (2004) Chem. Commun. , pp. 2208-2209
    • Booth, J.1    Cummins, W.J.2    Brown, T.3
  • 127
    • 0036861733 scopus 로고    scopus 로고
    • Oligonucleotides incorporating 7-(aminoalkynyl)-7-deaza-2'-deoxyguanosines: Duplex stability and phosphodiester hydrolysis by exonucleases
    • Rosemeyer, H.; Ramzaeva, N.; Becker, E.-M.; Feiling, E.; Seela, F. Oligonucleotides incorporating 7-(aminoalkynyl)-7-deaza-2'-deoxyguanosines: duplex stability and phosphodiester hydrolysis by exonucleases. Bioconjugate Chem., 2002, 13(6), 1274-1285.
    • (2002) Bioconjugate Chem , vol.13 , Issue.6 , pp. 1274-1285
    • Rosemeyer, H.1    Ramzaeva, N.2    Becker, E.-M.3    Feiling, E.4    Seela, F.5
  • 129
    • 40249111689 scopus 로고    scopus 로고
    • A new class of cleavable fluorescent nucleotides: Synthesis and optimization as reversible terminators for DNA sequencing by synthesis
    • Turcatti, G.; Romieu, A.; Fedurco, M.; Tairi, A.-P. A new class of cleavable fluorescent nucleotides: synthesis and optimization as reversible terminators for DNA sequencing by synthesis. Nucleic Acids Res., 2008, 36(4), e25.
    • (2008) Nucleic Acids Res , vol.36 , Issue.4
    • Turcatti, G.1    Romieu, A.2    Fedurco, M.3    Tairi, A.-P.4
  • 131
    • 77951239240 scopus 로고    scopus 로고
    • An integrated system for DNA sequencing by synthesis using novel nucleotide analogues
    • Guo, J.; Yu, L.; Turro, N. J.; Ju, J. An integrated system for DNA sequencing by synthesis using novel nucleotide analogues. Acc. Chem. Res., 2010, 43(4), 551-563.
    • (2010) Acc. Chem. Res. , vol.43 , Issue.4 , pp. 551-563
    • Guo, J.1    Yu, L.2    Turro, N.J.3    Ju, J.4
  • 132
    • 33644662470 scopus 로고    scopus 로고
    • Design and synthesis of a chemically cleavable fluorescent nucleotide, 3'-O-Allyl-dGTP-allyl-Bodipy-FL-510, as a reversible terminator for DNA sequencing by synthesis
    • Bi, L.; Kim, D. H.; Ju, J. Design and synthesis of a chemically cleavable fluorescent nucleotide, 3'-O-Allyl-dGTP-allyl-Bodipy-FL-510, as a reversible terminator for DNA sequencing by synthesis. J. Am. Chem. Soc., 2006, 128(8), 2542-2543.
    • (2006) J. Am. Chem. Soc. , vol.128 , Issue.8 , pp. 2542-2543
    • Bi, L.1    Kim, D.H.2    Ju, J.3
  • 133
    • 33645753463 scopus 로고    scopus 로고
    • Design and synthesis of a photocleavable fluorescent nucleotide 3'-O-allyl-dGTP-PCBodipy-FL-510 as a reversible terminator for DNA sequencing by synthesis
    • Meng, Q.; Kim, D. H.; Bai, X.; Bi, L.; Turro, N. J.; Ju, J. Design and synthesis of a photocleavable fluorescent nucleotide 3'-O-allyl-dGTP-PCBodipy-FL-510 as a reversible terminator for DNA sequencing by synthesis. J. Org. Chem., 2006, 71(8), 3248-3252.
    • (2006) J. Org. Chem. , vol.71 , Issue.8 , pp. 3248-3252
    • Meng, Q.1    Kim, D.H.2    Bai, X.3    Bi, L.4    Turro, N.J.5    Ju, J.6
  • 135
    • 84943999252 scopus 로고
    • Kinetics and reaction mechanisms: Selected examples from the experience of forty years
    • Huisgen, R. Kinetics and reaction mechanisms: selected examples from the experience of forty years. Pure Appl. Chem., 1989, 61(4), 613-628.
    • (1989) Pure Appl. Chem. , vol.61 , Issue.4 , pp. 613-628
    • Huisgen, R.1
  • 136
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • Rostovtsev, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew. Chem. Int. Ed., 2002, 41(14), 2596-2599.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , Issue.14 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 137
    • 70349144073 scopus 로고    scopus 로고
    • Cu(I)-catalyzed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in nucleoside, nucleotide, and oligonucleotide chemistry
    • Amblard, F.; Cho, J. H.; Schinazi, R. F. Cu(I)-catalyzed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in nucleoside, nucleotide, and oligonucleotide chemistry. Chem. Rev., 2009, 109(9), 4207-4220.
    • (2009) Chem. Rev. , vol.109 , Issue.9 , pp. 4207-4220
    • Amblard, F.1    Cho, J.H.2    Schinazi, R.F.3
  • 138
    • 0030768415 scopus 로고    scopus 로고
    • 7-Deazaguanine DNA: Oligonucleotides with hydrophobic or cationic side chains
    • Ramzaeva, N.; Mittelbach, C.; Seela, F. 7-Deazaguanine DNA: Oligonucleotides with hydrophobic or cationic side chains. Helv. Chim. Acta, 1997, 80(6), 1809-1822.
    • (1997) Helv. Chim. Acta. , vol.80 , Issue.6 , pp. 1809-1822
    • Ramzaeva, N.1    Mittelbach, C.2    Seela, F.3
  • 139
    • 38949201273 scopus 로고    scopus 로고
    • Modification of DNA with octadiynyl side chains: Synthesis, base pairing, and formation of fluorescent coumarin dye conjugates of four nucleobases by the alkyne-azide "click" reaction
    • Seela, F.; Sirivolu, V. R.; Chittepu, P. Modification of DNA with octadiynyl side chains: synthesis, base pairing, and formation of fluorescent coumarin dye conjugates of four nucleobases by the alkyne-azide "click" reaction. Bioconjugate Chem., 2008, 19(1), 211-224.
    • (2008) Bioconjugate Chem , vol.19 , Issue.1 , pp. 211-224
    • Seela, F.1    Sirivolu, V.R.2    Chittepu, P.3
  • 140
    • 75349096354 scopus 로고    scopus 로고
    • "Double click" reaction on 7-deazaguanine DNA: Synthesis and excimer fluorescence of nucleosides and oligonucleotides with branched side chains decorated with proximal pyrenes
    • Seela, F.; Ingale, S. A. "Double click" reaction on 7-deazaguanine DNA: synthesis and excimer fluorescence of nucleosides and oligonucleotides with branched side chains decorated with proximal pyrenes. J. Org. Chem., 2010, 75(2), 284-295.
    • (2010) J. Org. Chem. , vol.75 , Issue.2 , pp. 284-295
    • Seela, F.1    Ingale, S.A.2
  • 142
    • 0032720771 scopus 로고    scopus 로고
    • Oligonucleotides containing 7-deazaadenines: The influence of the 7-substituent chain length and charge on the duplex stability
    • Seela, F.; Zulauf, M. Oligonucleotides containing 7-deazaadenines: the influence of the 7-substituent chain length and charge on the duplex stability. Helv. Chim. Acta, 1999, 82(11), 1878-1898.
    • (1999) Helv. Chim. Acta. , vol.82 , Issue.11 , pp. 1878-1898
    • Seela, F.1    Zulauf, M.2
  • 143
    • 0034041226 scopus 로고    scopus 로고
    • 7-Substituted 7-deaza-2'-deoxyadenosines and 8-aza-7-deaza-2'-deoxyadenosines: Fluorescence of DNA-base analogues induced by the 7-alkynyl side chain
    • Seela, F.; Zulauf, M.; Sauer, M.; Deimel, M. 7-Substituted 7-deaza-2'-deoxyadenosines and 8-aza-7-deaza-2'-deoxyadenosines: fluorescence of DNA-base analogues induced by the 7-alkynyl side chain. Helv. Chim. Acta, 2000, 83(5), 910-927.
    • (2000) Helv. Chim. Acta. , vol.83 , Issue.5 , pp. 910-927
    • Seela, F.1    Zulauf, M.2    Sauer, M.3    Deimel, M.4
  • 145
    • 78649401529 scopus 로고    scopus 로고
    • Azide-alkyne click reaction performed on oligonucleotides with the universal nucleoside 7-octadiynyl-7-deaza-2'-deoxyinosine
    • Ming, X.; Leonard, P.; Heindl, D.; Seela, F. Azide-alkyne click reaction performed on oligonucleotides with the universal nucleoside 7-octadiynyl-7-deaza-2'-deoxyinosine. Nucleic Acids Symp. Ser., 2008, 52, 471-472.
    • (2008) Nucleic Acids Symp. Ser. , vol.52 , pp. 471-472
    • Ming, X.1    Leonard, P.2    Heindl, D.3    Seela, F.4
  • 146
    • 55449112419 scopus 로고    scopus 로고
    • Oligonucleotides containing 7-deaza-2'-deoxyinosine as universal nucleoside: Synthesis of 7-halogenated and 7-alkynylated derivatives, ambiguous base pairing, and dye functionalization by the alkyne-azide 'click' reaction
    • Seela, F.; Ming, X. Oligonucleotides containing 7-deaza-2'-deoxyinosine as universal nucleoside: synthesis of 7-halogenated and 7-alkynylated derivatives, ambiguous base pairing, and dye functionalization by the alkyne-azide 'click' reaction. Helv. Chim. Acta, 2008, 91(7), 1181-1200.
    • (2008) Helv. Chim. Acta. , vol.91 , Issue.7 , pp. 1181-1200
    • Seela, F.1    Ming, X.2
  • 147
    • 13844255131 scopus 로고    scopus 로고
    • Oligonucleotides containing 7-propynyl-7-deazaguanine: Synthesis and base pair stability
    • Seela, F.; Shaikh, K. I. Oligonucleotides containing 7-propynyl-7-deazaguanine: synthesis and base pair stability. Tetrahedron, 2005, 61(10), 2675-2681.
    • (2005) Tetrahedron , vol.61 , Issue.10 , pp. 2675-2681
    • Seela, F.1    Shaikh, K.I.2
  • 148
    • 29144491708 scopus 로고    scopus 로고
    • Stabilization of tandem dG-dA base pairs in DNA-hairpins: Replacement of the canonical bases by 7-deaza-7-propynylpurines
    • Seela, F.; Budow, S.; Shaikh, K. I.; Jawalekar, A. M. Stabilization of tandem dG-dA base pairs in DNA-hairpins: replacement of the canonical bases by 7-deaza-7-propynylpurines. Org. Biomol. Chem., 2005, 3(23), 4221-4226.
    • (2005) Org. Biomol. Chem. , vol.3 , Issue.23 , pp. 4221-4226
    • Seela, F.1    Budow, S.2    Shaikh, K.I.3    Jawalekar, A.M.4
  • 150
    • 36649009517 scopus 로고    scopus 로고
    • Ferrocenylethynyl derivatives of nucleoside triphosphates: Synthesis, incorporation, electrochemistry, and bioanalytical applications
    • Brázdilová, P.; Vrábel, M.; Pohl, R.; Pivoňková, H.; Havran, L.; Hocek, M.; Fojta, M. Ferrocenylethynyl derivatives of nucleoside triphosphates: synthesis, incorporation, electrochemistry, and bioanalytical applications. Chem. Eur. J., 2007, 13(34), 9527-9533.
    • (2007) Chem. Eur. J. , vol.13 , Issue.34 , pp. 9527-9533
    • Brázdilová, P.1    Vrábel, M.2    Pohl, R.3    Pivoňková, H.4    Havran, L.5    Hocek, M.6    Fojta, M.7
  • 152
    • 77149150613 scopus 로고    scopus 로고
    • Synthesis of nucleoside and nucleotide conjugates of bile acids, and polymerase construction of bile acid-functionalized DNA
    • Ikonen, S.; Macíčková-Cahová, H.; Pohl, R.; Šanda, M.; Hocek, M. Synthesis of nucleoside and nucleotide conjugates of bile acids, and polymerase construction of bile acid-functionalized DNA. Org. Biomol. Chem., 2010, 8(5), 1194-1201.
    • (2010) Org. Biomol. Chem. , vol.8 , Issue.5 , pp. 1194-1201
    • Ikonen, S.1    Macíčková-Cahová, H.2    Pohl, R.3    Šanda, M.4    Hocek, M.5
  • 153
    • 34547208319 scopus 로고    scopus 로고
    • An efficient method for the construction of functionalized DNA bearing amino acid groups through cross-coupling reactions of nucleoside triphosphates followed by primer extension or PCR
    • Čapek, P.; Cahová, H.; Pohl, R.; Hocek, M.; Gloeckner, C.; Marx, A. An efficient method for the construction of functionalized DNA bearing amino acid groups through cross-coupling reactions of nucleoside triphosphates followed by primer extension or PCR. Chem. Eur. J., 2007, 13(21), 6196-6203.
    • (2007) Chem. Eur. J. , vol.13 , Issue.21 , pp. 6196-6203
    • Čapek, P.1    Cahová, H.2    Pohl, R.3    Hocek, M.4    Gloeckner, C.5    Marx, A.6
  • 154
    • 49249108561 scopus 로고    scopus 로고
    • Synthesis and photophysical properties of 7-deaza-2'-deoxyadenosines bearing bipyridine ligands and their Ru(II)-complexes in position 7
    • Vrábel, M.; Pohl, R.; Votruba, I.; Sajadi, M.; Kovalenko, S. A.; Ernsting, N. P.; Hocek, M. Synthesis and photophysical properties of 7-deaza-2'-deoxyadenosines bearing bipyridine ligands and their Ru(II)-complexes in position 7. Org. Biomol. Chem., 2008, 6(16), 2852-2860.
    • (2008) Org. Biomol. Chem. , vol.6 , Issue.16 , pp. 2852-2860
    • Vrábel, M.1    Pohl, R.2    Votruba, I.3    Sajadi, M.4    Kovalenko, S.A.5    Ernsting, N.P.6    Hocek, M.7
  • 155
    • 41949124411 scopus 로고    scopus 로고
    • Aminophenyl- and nitrophenyl-labeled nucleoside triphosphates: Synthesis, enzymatic incorporation, and electrochemical detection
    • Cahová, H.; Havran, L.; Brázdilová, P.; Pivoňková, H.; Pohl, R.; Fojta, M.; Hocek, M. Aminophenyl- and nitrophenyl-labeled nucleoside triphosphates: synthesis, enzymatic incorporation, and electrochemical detection. Angew. Chem. Int. Ed., 2008, 47(11), 2059-2062.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 2059-2062
    • Cahová, H.1    Havran, L.2    Brázdilová, P.3    Pivoňková, H.4    Pohl, R.5    Fojta, M.6    Hocek, M.7
  • 156
    • 76249129616 scopus 로고    scopus 로고
    • Direct polymerase synthesis of reactive aldehyde-functionalized DNA and its conjugation and staining with hydrazines
    • Raindlová, V.; Pohl, R.; Šanda, M.; Hocek, M. Direct polymerase synthesis of reactive aldehyde-functionalized DNA and its conjugation and staining with hydrazines. Angew. Chem. Int. Ed., 2010, 49(6), 1064-1066.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , Issue.6 , pp. 1064-1066
    • Raindlová, V.1    Pohl, R.2    Šanda, M.3    Hocek, M.4
  • 159
    • 51049094897 scopus 로고    scopus 로고
    • Cu-catalyzed azide-alkyne cycloaddition
    • Meldal, M.; Tornøe, C. W. Cu-catalyzed azide-alkyne cycloaddition. Chem. Rev., 2008, 108(8), 2952-3015.
    • (2008) Chem. Rev. , vol.108 , Issue.8 , pp. 2952-3015
    • Meldal, M.1    Tornøe, C.W.2
  • 160
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click chemistry: diverse chemical function from a few good reactions. Angew. Chem. Int. Ed., 2001, 40(11), 2004-2021.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , Issue.11 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 161
    • 34547272503 scopus 로고    scopus 로고
    • The growing applications of click chemistry
    • Moses, J. E.; Moorhouse, A. D. The growing applications of click chemistry. Chem. Soc. Rev., 2007, 36(8), 1249-1262.
    • (2007) Chem. Soc. Rev , vol.36 , Issue.8 , pp. 1249-1262
    • Moses, J.E.1    Moorhouse, A.D.2
  • 162
    • 34250023096 scopus 로고    scopus 로고
    • Nucleosides and oligonucleotides with diynyl side chains: Base pairing and functionalization of 2'-deoxyuridine derivatives by the copper(I)-catalyzed alkyne azide 'click' cycloaddition
    • Seela, F.; Sirivolu, V. R. Nucleosides and oligonucleotides with diynyl side chains: base pairing and functionalization of 2'-deoxyuridine derivatives by the copper(I)-catalyzed alkyne azide 'click' cycloaddition. Helv. Chim. Acta, 2007, 90(3), 535-552.
    • (2007) Helv. Chim. Acta. , vol.90 , Issue.3 , pp. 535-552
    • Seela, F.1    Sirivolu, V.R.2
  • 163
    • 33745018158 scopus 로고    scopus 로고
    • DNA containing side chains with terminal triple bonds: Base pair stability and functionalization of alkynylated pyrimidines and 7-deazapurines
    • Seela, F.; Sirivolu, V. R. DNA containing side chains with terminal triple bonds: base pair stability and functionalization of alkynylated pyrimidines and 7-deazapurines. Chem. Biodivers., 2006, 3, 509-514.
    • (2006) Chem. Biodivers. , vol.3 , pp. 509-514
    • Seela, F.1    Sirivolu, V.R.2
  • 164
    • 0348109450 scopus 로고    scopus 로고
    • The growing impact of click chemistry on drug discovery
    • Kolb, H. C.; Sharpless, K. B. The growing impact of click chemistry on drug discovery. Drug Discov. Today, 2003, 8(24), 1128-1137.
    • (2003) Drug Discov. Today , vol.8 , Issue.24 , pp. 1128-1137
    • Kolb, H.C.1    Sharpless, K.B.2
  • 165
    • 54249161798 scopus 로고    scopus 로고
    • Postsynthetic DNA modification through the copper-catalyzed azide-alkyne cycloaddition reaction
    • Gramlich, P. M. E.; Wirges, C. T.; Manetto, A.; Carell, T. Postsynthetic DNA modification through the copper-catalyzed azide-alkyne cycloaddition reaction. Angew. Chem. Int. Ed., 2008, 47(44), 8350-8358.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , Issue.44 , pp. 8350-8358
    • Gramlich, P.M.E.1    Wirges, C.T.2    Manetto, A.3    Carell, T.4
  • 166
    • 37549059930 scopus 로고    scopus 로고
    • A versatile method for the preparation of conjugates of peptides with DNA/PNA/analog by employing chemo-selective click reaction in water
    • Gogoi, K.; Mane, M. V.; Kunte, S. S.; Kumar, V. A. A versatile method for the preparation of conjugates of peptides with DNA/PNA/analog by employing chemo-selective click reaction in water. Nucleic Acids Res., 2007, 35(21), e139.
    • (2007) Nucleic Acids Res , vol.35 , Issue.21
    • Gogoi, K.1    Mane, M.V.2    Kunte, S.S.3    Kumar, V.A.4
  • 167
    • 51449095749 scopus 로고    scopus 로고
    • Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: Synthesis via the azide-alkyne 'click' reaction
    • Chittepu, P.; Sirivolu, V. R.; Seela, F. Nucleosides and oligonucleotides containing 1,2,3-triazole residues with nucleobase tethers: synthesis via the azide-alkyne 'click' reaction. Biorg. Med. Chem., 2008, 16(18), 8427-8439.
    • (2008) Biorg. Med. Chem. , vol.16 , Issue.18 , pp. 8427-8439
    • Chittepu, P.1    Sirivolu, V.R.2    Seela, F.3
  • 169
    • 64549094682 scopus 로고    scopus 로고
    • Synthesis of mannose and galactose oligonucleotide conjugates by bi-click chemistry
    • Pourceau, G.; Meyer, A.; Vasseur, J.-J.; Morvan, F. Synthesis of mannose and galactose oligonucleotide conjugates by bi-click chemistry. J. Org. Chem., 2009, 74(3), 1218-1222.
    • (2009) J. Org. Chem. , vol.74 , Issue.3 , pp. 1218-1222
    • Pourceau, G.1    Meyer, A.2    Vasseur, J.-J.3    Morvan, F.4
  • 170
    • 33744925392 scopus 로고    scopus 로고
    • Microwave assisted "click" chemistry for the synthesis of multiple labeled-carbohydrate oligonucleotides on solid support
    • Bouillon, C.; Meyer, A.; Vidal, S.; Jochum, A.; Chevolot, Y.; Cloarec, J.-P.; Praly, J.-P.; Vasseur, J.-J.; Morvan, F. Microwave assisted "click" chemistry for the synthesis of multiple labeled-carbohydrate oligonucleotides on solid support. J. Org. Chem., 2006, 71(12), 4700-4702.
    • (2006) J. Org. Chem. , vol.71 , Issue.12 , pp. 4700-4702
    • Bouillon, C.1    Meyer, A.2    Vidal, S.3    Jochum, A.4    Chevolot, Y.5    Cloarec, J.-P.6    Praly, J.-P.7    Vasseur, J.-J.8    Morvan, F.9
  • 171
    • 67649231388 scopus 로고    scopus 로고
    • Solid-phase synthesis of oligonucleotide conjugates useful for delivery and targeting of potential nucleic acid therapeutics
    • Lönnberg, H. Solid-phase synthesis of oligonucleotide conjugates useful for delivery and targeting of potential nucleic acid therapeutics. Bioconjugate Chem., 2009, 20(6), 1065-1094.
    • (2009) Bioconjugate Chem , vol.20 , Issue.6 , pp. 1065-1094
    • Lönnberg, H.1
  • 173
    • 1842631432 scopus 로고    scopus 로고
    • Photocleavable fluorescent nucleotides for DNA sequencing on a chip constructed by sitespecific coupling chemistry
    • Seo, T. S.; Bai, X.; Ruparel, H.; Li, Z.; Turro, N. J.; Ju, J. Photocleavable fluorescent nucleotides for DNA sequencing on a chip constructed by sitespecific coupling chemistry. Proc. Natl. Acad. Sci. USA, 2004, 101(15), 5488-5493.
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , Issue.15 , pp. 5488-5493
    • Seo, T.S.1    Bai, X.2    Ruparel, H.3    Li, Z.4    Turro, N.J.5    Ju, J.6
  • 175
    • 1442357313 scopus 로고    scopus 로고
    • "Clicking" functionality onto electrode surfaces
    • Collman, J. P.; Devaraj, N. K.; Chidsey, C. E. D. "Clicking" functionality onto electrode surfaces. Langmuir, 2004, 20(4), 1051-1053.
    • (2004) Langmuir , vol.20 , Issue.4 , pp. 1051-1053
    • Collman, J.P.1    Devaraj, N.K.2    Chidsey, C.E.D.3
  • 176
    • 78049361650 scopus 로고    scopus 로고
    • Spatially controlled DNA nanopatterns by "click" chemistry using oligonucleotides with different anchoring sites
    • Qing, G.; Xiong, H.; Seela, F.; Sun, T. Spatially controlled DNA nanopatterns by "click" chemistry using oligonucleotides with different anchoring sites. J. Am. Chem. Soc., 2010, 132(43), 15228-15232.
    • (2010) J. Am. Chem. Soc. , vol.132 , Issue.43 , pp. 15228-15232
    • Qing, G.1    Xiong, H.2    Seela, F.3    Sun, T.4
  • 177
    • 38749149967 scopus 로고    scopus 로고
    • Synthesis of modified DNA by PCR with alkyne-bearing purines followed by a click reaction
    • Gramlich, P. M. E.; Wirges, C. T.; Gierlich, J.; Carell, T. Synthesis of modified DNA by PCR with alkyne-bearing purines followed by a click reaction. Org. Lett., 2007, 10(2), 249-251.
    • (2007) Org. Lett. , vol.10 , Issue.2 , pp. 249-251
    • Gramlich, P.M.E.1    Wirges, C.T.2    Gierlich, J.3    Carell, T.4
  • 181
    • 77956621001 scopus 로고    scopus 로고
    • Azide-alkyne "click" conjugation of 8-aza-7-deazaadenine-DNA: Synthesis, duplex stability, and fluorogenic dye labeling
    • Seela, F.; Pujari, S. S. Azide-alkyne "click" conjugation of 8-aza-7-deazaadenine-DNA: synthesis, duplex stability, and fluorogenic dye labeling. Bioconjugate Chem., 2010, 21(9), 1629-1641.
    • (2010) Bioconjugate Chem , vol.21 , Issue.9 , pp. 1629-1641
    • Seela, F.1    Pujari, S.S.2
  • 182
    • 67649319499 scopus 로고    scopus 로고
    • 8-Aza-7-deazaguanine nucleosides and oligonucleotides with octadiynyl side chains: Synthesis, functionalization by the azide-alkyne 'click' reaction and nucleobase specific fluorescence quenching of coumarin dye conjugates
    • Seela, F.; Xiong, H.; Leonard, P.; Budow, S. 8-Aza-7-deazaguanine nucleosides and oligonucleotides with octadiynyl side chains: synthesis, functionalization by the azide-alkyne 'click' reaction and nucleobase specific fluorescence quenching of coumarin dye conjugates. Org. Biomol. Chem., 2009, 7(7), 1374-1387.
    • (2009) Org. Biomol. Chem. , vol.7 , Issue.7 , pp. 1374-1387
    • Seela, F.1    Xiong, H.2    Leonard, P.3    Budow, S.4
  • 183
    • 0346379668 scopus 로고
    • A simple synthesis of 4-amino-2,2,6,6-tetramethyl-1-piperidinyloxy radical
    • Bushmakina, N. G.; Misharin, A. Y. A simple synthesis of 4-amino-2,2,6,6-tetramethyl-1-piperidinyloxy radical. Synthesis, 1986, 966.
    • (1986) Synthesis , pp. 966
    • Bushmakina, N.G.1    Misharin, A.Y.2
  • 184
    • 78651230745 scopus 로고    scopus 로고
    • Site-directed spin-labeling of DNA by the azide-alkyne 'click' reaction: Nanometer distance measurements on 7-deaza-2'-deoxyadenosine and 2'-deoxyuridine nitroxide conjugates spatially separated or linked to a 'dA-dT' base pair
    • Ding, P.; Wunnicke, D.; Steinhoff, H.-J.; Seela, F. Site-directed spin-labeling of DNA by the azide-alkyne 'click' reaction: nanometer distance measurements on 7-deaza-2'-deoxyadenosine and 2'-deoxyuridine nitroxide conjugates spatially separated or linked to a 'dA-dT' base pair. Chem. Eur. J., 2010, 16(48), 14385-14396.
    • (2010) Chem. Eur. J. , vol.16 , Issue.48 , pp. 14385-14396
    • Ding, P.1    Wunnicke, D.2    Steinhoff, H.-J.3    Seela, F.4
  • 185
    • 77949779995 scopus 로고    scopus 로고
    • Click chemistry with DNA
    • El-Sagheer, A. H.; Brown, T. Click chemistry with DNA. Chem. Soc. Rev., 2010, 39(4), 1388-1405.
    • (2010) Chem. Soc. Rev. , vol.39 , Issue.4 , pp. 1388-1405
    • El-Sagheer, A.H.1    Brown, T.2
  • 186
    • 34249794857 scopus 로고    scopus 로고
    • Template-directed oligonucleotide strand ligation, covalent intramolecular DNA circularization and catenation using click chemistry
    • Kumar, R.; El-Sagheer, A.; Tumpane, J.; Lincoln, P.; Wilhelmsson, L. M.; Brown, T. Template-directed oligonucleotide strand ligation, covalent intramolecular DNA circularization and catenation using click chemistry. J. Am. Chem. Soc., 2007, 129(21), 6859-6864.
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.21 , pp. 6859-6864
    • Kumar, R.1    El-Sagheer, A.2    Tumpane, J.3    Lincoln, P.4    Wilhelmsson, L.M.5    Brown, T.6
  • 187
    • 37549013666 scopus 로고    scopus 로고
    • New strategies for cyclization and bicyclization of oligonucleotides by click chemistry assisted by microwaves
    • Lietard, J.; Meyer, A.; Vasseur, J.-J.; Morvan, F. New strategies for cyclization and bicyclization of oligonucleotides by click chemistry assisted by microwaves. J. Org. Chem., 2008, 73(1), 191-200.
    • (2008) J. Org. Chem. , vol.73 , Issue.1 , pp. 191-200
    • Lietard, J.1    Meyer, A.2    Vasseur, J.-J.3    Morvan, F.4
  • 188
    • 77955000685 scopus 로고    scopus 로고
    • A template-mediated click-click reaction: PNA-DNA, PNA-PNA (or peptide) ligation, and single nucleotide discrimination
    • Peng, X.; Li, H.; Seidman, M. A template-mediated click-click reaction: PNA-DNA, PNA-PNA (or peptide) ligation, and single nucleotide discrimination. Eur. J. Org. Chem., 2010, 4194-4197.
    • (2010) Eur. J. Org. Chem. , pp. 4194-4197
    • Peng, X.1    Li, H.2    Seidman, M.3
  • 189
    • 60849106672 scopus 로고    scopus 로고
    • Generation of DNA interstrand cross-links by post-synthetic reductive amination
    • Angelov, T.; Guainazzi, A.; Schärer, O. D. Generation of DNA interstrand cross-links by post-synthetic reductive amination. Org. Lett., 2009, 11(3), 661-664.
    • (2009) Org. Lett. , vol.11 , Issue.3 , pp. 661-664
    • Angelov, T.1    Guainazzi, A.2    Schärer, O.D.3
  • 190
    • 78650318528 scopus 로고    scopus 로고
    • Cross-linked DNA generated by "bis-click" reactions with bis-functional azides: Site independent ligation of oligonucleotides via nucleobase alkynyl chains
    • Pujari, S. S.; Xiong, H.; Seela, F. Cross-linked DNA generated by "bis-click" reactions with bis-functional azides: site independent ligation of oligonucleotides via nucleobase alkynyl chains. J. Org. Chem., 2010, 75(24), 8693-8696.
    • (2010) J. Org. Chem. , vol.75 , Issue.24 , pp. 8693-8696
    • Pujari, S.S.1    Xiong, H.2    Seela, F.3
  • 191
    • 0028322189 scopus 로고
    • Summary: The modified nucleosides of RNA
    • Limbach, P. A.; Crain, P. F.; McCloskey, J. A. Summary: the modified nucleosides of RNA. Nucleic Acids Res., 1994, 22(12), 2183-2196.
    • (1994) Nucleic Acids Res , vol.22 , Issue.12 , pp. 2183-2196
    • Limbach, P.A.1    Crain, P.F.2    McCloskey, J.A.3
  • 192
    • 0030755275 scopus 로고    scopus 로고
    • Regioselectivity of the Mannich reaction on pyrrolo[2,3-d] pyrimidine nucleosides related to 7-deaza-2'-deoxyadenosine or 7-deaza-2'-deoxyguanosine
    • Seela, F.; Chen, Y.; Zulauf, M. Regioselectivity of the Mannich reaction on pyrrolo[2,3-d] pyrimidine nucleosides related to 7-deaza-2'-deoxyadenosine or 7-deaza-2'-deoxyguanosine. Synthesis, 1997, 1067-1072.
    • (1997) Synthesis , pp. 1067-1072
    • Seela, F.1    Chen, Y.2    Zulauf, M.3
  • 193
    • 0022423163 scopus 로고
    • Solid-phase synthesis of the self-complementary hexamer d(c7GpCpc7GpCpc7GpC) via the O-3'-phosphoramidite of 7-deaza-2'-deoxyguanosine
    • Seela, F.; Driller, H. Solid-phase synthesis of the self-complementary hexamer d(c7GpCpc7GpCpc7GpC) via the O-3'-phosphoramidite of 7-deaza-2'-deoxyguanosine. Nucleic Acids Res., 1985, 13(3), 911-926.
    • (1985) Nucleic Acids Res , vol.13 , Issue.3 , pp. 911-926
    • Seela, F.1    Driller, H.2
  • 198
    • 37049070069 scopus 로고
    • Total synthesis of 2'-deoxy-2'-arafluoro-tubercidin, -toyocamycin, -sangivamycin and certain related nucleosides
    • Bhattacharya, B. K.; Rao, T. S.; Revankar, G. R. Total synthesis of 2'-deoxy-2'-arafluoro-tubercidin, -toyocamycin, -sangivamycin and certain related nucleosides. J. Chem. Soc., Perkin Trans. 1, 1995, 1543-1550.
    • (1995) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1543-1550
    • Bhattacharya, B.K.1    Rao, T.S.2    Revankar, G.R.3
  • 199
    • 0028874503 scopus 로고
    • Synthesis and anti-DNA viral activities in vitro of certain 2,4-disubstituted-7-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidine nucleosides
    • Bhattacharya, B. K.; Ojwang, J. O.; Rando, R. F.; Huffman, J. H.; Revankar, G. R. Synthesis and anti-DNA viral activities in vitro of certain 2,4-disubstituted-7-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidine nucleosides. J. Med. Chem., 1995, 38(20), 3957-3966.
    • (1995) J. Med. Chem. , vol.38 , Issue.20 , pp. 3957-3966
    • Bhattacharya, B.K.1    Ojwang, J.O.2    Rando, R.F.3    Huffman, J.H.4    Revankar, G.R.5
  • 200
    • 0028887016 scopus 로고
    • Inhibition of episomal hepatitis B virus DNA in vitro by 2,4-diamino-7-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-pyrrolo[2,3-d]pyrimidine
    • Ojwang, J. O.; Bhattacharya, B. K.; Marshall, H. B.; Korba, B. E.; Revankar, G. R.; Rando, R. F. Inhibition of episomal hepatitis B virus DNA in vitro by 2,4-diamino-7-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-pyrrolo[2,3-d]pyrimidine. Antimicrob. Agents Chemother., 1995, 39(11), 2570-2573.
    • (1995) Antimicrob. Agents Chemother. , vol.39 , Issue.11 , pp. 2570-2573
    • Ojwang, J.O.1    Bhattacharya, B.K.2    Marshall, H.B.3    Korba, B.E.4    Revankar, G.R.5    Rando, R.F.6
  • 201
    • 0002642858 scopus 로고
    • Antiviral nucleosides. A stereospecific, total synthesis of 2'-fluoro-2'-deoxy-β-D-arabinofuranosyl nucleosides
    • Howell, H. G.; Brodfuehrer, P. R.; Brundidge, S. P.; Benigni, D. A.; Sapino, Jr., C. Antiviral nucleosides. A stereospecific, total synthesis of 2'-fluoro-2'-deoxy-β-D-arabinofuranosyl nucleosides. J. Org. Chem., 1988, 53(1), 85-88.
    • (1988) J. Org. Chem. , vol.53 , Issue.1 , pp. 85-88
    • Howell, H.G.1    Brodfuehrer, P.R.2    Brundidge, S.P.3    Benigni, D.A.4    Sapino, C.5
  • 202
    • 6344238718 scopus 로고    scopus 로고
    • Halogenated 7-deazapurine nucleosides: Stereoselective synthesis and conformation of 2'-deoxy-2'-fluoro-β-D-arabinonucleosides
    • Peng, X.; Seela, F. Halogenated 7-deazapurine nucleosides: stereoselective synthesis and conformation of 2'-deoxy-2'-fluoro-β-D-arabinonucleosides. Org. Biomol. Chem., 2004, 2(19), 2838-2846.
    • (2004) Org. Biomol. Chem. , vol.2 , Issue.19 , pp. 2838-2846
    • Peng, X.1    Seela, F.2
  • 203
    • 0028863914 scopus 로고
    • Synthesis and antiproliferative and antiviral activity of 2'-deoxy-2'-fluoroarabinofuranosyl analogs of the nucleoside antibiotics toyocamycin and sangivamycin
    • Krawczyk, S. H.; Nassiri, M. R.; Kucera, L. S.; Kern, E. R.; Ptak, R. G.; Wotring, L. L.; Drach, J. C.; Townsend, L. B. Synthesis and antiproliferative and antiviral activity of 2'-deoxy-2'-fluoroarabinofuranosyl analogs of the nucleoside antibiotics toyocamycin and sangivamycin. J. Med. Chem., 1995, 38(20), 4106-4114.
    • (1995) J. Med. Chem. , vol.38 , Issue.20 , pp. 4106-4114
    • Krawczyk, S.H.1    Nassiri, M.R.2    Kucera, L.S.3    Kern, E.R.4    Ptak, R.G.5    Wotring, L.L.6    Drach, J.C.7    Townsend, L.B.8
  • 204
    • 0040609327 scopus 로고    scopus 로고
    • Adenosine deaminase prefers a distinct sugar ring conformation for binding and catalysis: Kinetic and structural studies
    • Ford, Jr., H.; Dai, F.; Mu, L.; Siddiqui, M. A.; Nicklaus, M. C.; Anderson, L.; Marquez, V. E.; Barchi, Jr., J. J. Adenosine deaminase prefers a distinct sugar ring conformation for binding and catalysis: kinetic and structural studies. Biochemistry, 2000, 39(10), 2581-2592.
    • (2000) Biochemistry , vol.39 , Issue.10 , pp. 2581-2592
    • Ford, H.1    Dai, F.2    Mu, L.3    Siddiqui, M.A.4    Nicklaus, M.C.5    Anderson, L.6    Marquez, V.E.7    Barchi, J.J.8
  • 209
    • 0024338599 scopus 로고
    • 2', 3'-Dideoxy-3'-fluorotubercidin and related dideoxyribonucleosides: Synthesis via a 2'-deoxy-3'-oxoribofuranoside intermediate and conformation studies
    • Rosemeyer, H.; Seela, F. 2', 3'-Dideoxy-3'-fluorotubercidin and related dideoxyribonucleosides: synthesis via a 2'-deoxy-3'-oxoribofuranoside intermediate and conformation studies. Helv. Chim. Acta, 1989, 72(5), 1084-1094.
    • (1989) Helv. Chim. Acta. , vol.72 , Issue.5 , pp. 1084-1094
    • Rosemeyer, H.1    Seela, F.2
  • 210
    • 0025868547 scopus 로고
    • 3'-Substituted and 2',3'-unsaturated 7-deazaguanine 2',3'-dideoxynucleosides: Syntheses and inhibition of HIV-1 reverse transcriptase
    • Seela, F.; Muth, H.-P. 3'-Substituted and 2',3'-unsaturated 7-deazaguanine 2',3'-dideoxynucleosides: syntheses and inhibition of HIV-1 reverse transcriptase. Helv. Chim. Acta, 1991, 74(5), 1081-1090.
    • (1991) Helv. Chim. Acta. , vol.74 , Issue.5 , pp. 1081-1090
    • Seela, F.1    Muth, H.-P.2
  • 211
    • 84986694082 scopus 로고
    • Synthesis of 4-substituted 2-aminopyrrolo-[2,3-d]pyrimidine 2',3'-dideoxyribonucleosides
    • Seela, F.; Muth, H.-P. Synthesis of 4-substituted 2-aminopyrrolo-[2,3-d]pyrimidine 2',3'-dideoxyribonucleosides. Liebigs Ann. Chem., 1990, 227-232.
    • (1990) Liebigs Ann. Chem. , pp. 227-232
    • Seela, F.1    Muth, H.-P.2
  • 212
    • 0019760168 scopus 로고
    • A new route to nucleoside 5'-triphosphates
    • Ludwig, J. A new route to nucleoside 5'-triphosphates. Acta Biochim. Biophys. Acad. Sci. Hung., 1981, 16(3-4), 131-133.
    • (1981) Acta Biochim. Biophys. Acad. Sci. Hung. , vol.16 , Issue.3-4 , pp. 131-133
    • Ludwig, J.1
  • 213
    • 0014619339 scopus 로고
    • Enzymatic synthesis of deoxyribonucleic acid. XXXIV. Termination of chain growth by a 2',3'-dideoxyribonucleotide
    • Atkinson, M. R.; Deutscher, M. P.; Kornberg, A.; Russell, A. F.; Moffatt, J. G. Enzymatic synthesis of deoxyribonucleic acid. XXXIV. Termination of chain growth by a 2',3'-dideoxyribonucleotide. Biochemistry, 1969, 8(12), 4897-4904.
    • (1969) Biochemistry , vol.8 , Issue.12 , pp. 4897-4904
    • Atkinson, M.R.1    Deutscher, M.P.2    Kornberg, A.3    Russell, A.F.4    Moffatt, J.G.5
  • 214
    • 0019857853 scopus 로고
    • Role of DNA polymerase γ in adenovirus DNA replication. Mechanism of inhibition by 2',3'-dideoxynucleoside 5'-triphosphates
    • van der Vliet, P. C.; Kwant, M. M. Role of DNA polymerase γ in adenovirus DNA replication. Mechanism of inhibition by 2',3'-dideoxynucleoside 5'-triphosphates. Biochemistry, 1981, 20(9), 2628-2632.
    • (1981) Biochemistry , vol.20 , Issue.9 , pp. 2628-2632
    • van der Vliet, P.C.1    Kwant, M.M.2
  • 215
    • 0021179075 scopus 로고
    • Effects of 2',3'-dideoxynucleosides on mammalian cells and viruses
    • Waqar, M. A.; Evans, M. J.; Manly, K. F.; Hughes, R. G.; Huberman, J. A. Effects of 2',3'-dideoxynucleosides on mammalian cells and viruses. J. Cell. Physiol., 1984, 121(2), 402-408.
    • (1984) J. Cell. Physiol. , vol.121 , Issue.2 , pp. 402-408
    • Waqar, M.A.1    Evans, M.J.2    Manly, K.F.3    Hughes, R.G.4    Huberman, J.A.5
  • 216
    • 0015240470 scopus 로고
    • Direction of polymerization by the avian myeloblastosis virus deoxyribonucleic acid polymerase
    • Smoler, D.; Molineux, I.; Baltimore, D. Direction of polymerization by the avian myeloblastosis virus deoxyribonucleic acid polymerase. J. Biol. Chem., 1971, 246(24), 7697-7700.
    • (1971) J. Biol. Chem. , vol.246 , Issue.24 , pp. 7697-7700
    • Smoler, D.1    Molineux, I.2    Baltimore, D.3
  • 217
    • 0001587762 scopus 로고
    • Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2',3'-dideoxynucleosides
    • Mitsuya, H.; Broder, S. Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2',3'-dideoxynucleosides. Proc. Natl. Acad. Sci. USA, 1986, 83(6), 1911-1915.
    • (1986) Proc. Natl. Acad. Sci. USA , vol.83 , Issue.6 , pp. 1911-1915
    • Mitsuya, H.1    Broder, S.2
  • 218
    • 0022552064 scopus 로고
    • Chemotherapeutic approaches to the treatment of the acquired immune deficiency syndrome (AIDS)
    • De Clercq, E. Chemotherapeutic approaches to the treatment of the acquired immune deficiency syndrome (AIDS). J. Med. Chem., 1986, 29(9), 1561-1569.
    • (1986) J. Med. Chem. , vol.29 , Issue.9 , pp. 1561-1569
    • de Clercq, E.1
  • 220
    • 0017681196 scopus 로고
    • DNA sequencing with chainterminating inhibitors
    • Sanger, F.; Nicklen, S.; Coulson, A. R. DNA sequencing with chainterminating inhibitors. Proc. Natl. Acad. Sci. USA, 1977, 74(12), 5463-5467.
    • (1977) Proc. Natl. Acad. Sci. USA , vol.74 , Issue.12 , pp. 5463-5467
    • Sanger, F.1    Nicklen, S.2    Coulson, A.R.3
  • 224
    • 0026426081 scopus 로고
    • Three DNA sequencing methods using capillary gel electrophoresis and laser-induced fluorescence
    • Swerdlow, H.; Zhang, J. Z.; Chen, D. Y.; Harke, H. R.; Grey, R.; Wu, S.; Dovichi, N. J.; Fuller, C. Three DNA sequencing methods using capillary gel electrophoresis and laser-induced fluorescence. Anal. Chem., 1991, 63(24), 2835-2841.
    • (1991) Anal. Chem. , vol.63 , Issue.24 , pp. 2835-2841
    • Swerdlow, H.1    Zhang, J.Z.2    Chen, D.Y.3    Harke, H.R.4    Grey, R.5    Wu, S.6    Dovichi, N.J.7    Fuller, C.8
  • 225
    • 0035886661 scopus 로고    scopus 로고
    • Capillary gel electrophoresis with sinusoidal voltammetric detection:A strategy to allow four-"color" DNA sequencing
    • Brazill, S. A.; Kim, P. H.; Kuhr, W. G. Capillary gel electrophoresis with sinusoidal voltammetric detection:a strategy to allow four-"color" DNA sequencing. Anal. Chem., 2001, 73(20), 4882-4890.
    • (2001) Anal. Chem. , vol.73 , Issue.20 , pp. 4882-4890
    • Brazill, S.A.1    Kim, P.H.2    Kuhr, W.G.3
  • 226
    • 33845185176 scopus 로고
    • Palladium-catalyzed synthesis of alkynylamino nucleosides. A universal linker for nucleic acids
    • Hobbs, Jr., F. W. Palladium-catalyzed synthesis of alkynylamino nucleosides. A universal linker for nucleic acids. J. Org. Chem., 1989, 54(14), 3420-3422.
    • (1989) J. Org. Chem. , vol.54 , Issue.14 , pp. 3420-3422
    • Hobbs, F.W.1
  • 228
    • 0035511619 scopus 로고    scopus 로고
    • DNA sequencing using biotinylated dideoxynucleotides and mass spectrometry
    • Edwards, J. R.; Itagaki, Y.; Ju, J. DNA sequencing using biotinylated dideoxynucleotides and mass spectrometry. Nucleic Acids Res., 2001, 29(21), e104.
    • (2001) Nucleic Acids Res , vol.29 , Issue.21
    • Edwards, J.R.1    Itagaki, Y.2    Ju, J.3
  • 229
    • 84985208649 scopus 로고
    • Synthese von 7-Desaza-2',3'-didesoxyguanosin durch Desoxygenierung seines 2'-Desoxy-β-D-ribofuranosids
    • Seela, F.; Muth, H.-P. Synthese von 7-Desaza-2',3'-didesoxyguanosin durch Desoxygenierung seines 2'-Desoxy-β-D-ribofuranosids. Liebigs Ann. Chem., 1988, 215-219.
    • (1988) Liebigs Ann. Chem. , pp. 215-219
    • Seela, F.1    Muth, H.-P.2
  • 230
    • 0025279792 scopus 로고
    • Synthesis of 2',3'-didehydro-2',3'-dideoxyformycin A, 2',3'-dideoxyformycin A and 2',3'-dideoxytubercidin
    • Serafinowski, P. Synthesis of 2',3'-didehydro-2',3'-dideoxyformycin A, 2',3'-dideoxyformycin A and 2',3'-dideoxytubercidin. Synthesis, 1990, 411-415.
    • (1990) Synthesis , pp. 411-415
    • Serafinowski, P.1
  • 231
    • 84856465983 scopus 로고
    • Synthesis of pyrrolo[2,3-b]pyridine nucleosides by solid-liquid phase-transfer glycosylation and deoxygenation of 4-chloropyrrolo[2,3-d]pyrimidine 2'-deoxyribofuranosides
    • Seela, F.; Gumbiowski, R.; Muth, H.-P.; Bourgeois, W. Synthesis of pyrrolo[2,3-b]pyridine nucleosides by solid-liquid phase-transfer glycosylation and deoxygenation of 4-chloropyrrolo[2,3-d]pyrimidine 2'-deoxyribofuranosides. Nucleosides Nucleotides, 1989, 8(5), 1087-1088.
    • (1989) Nucleosides Nucleotides , vol.8 , Issue.5 , pp. 1087-1088
    • Seela, F.1    Gumbiowski, R.2    Muth, H.-P.3    Bourgeois, W.4
  • 232
    • 0023650529 scopus 로고
    • Synthesis of some S-3'-deoxyadenosyl-L-homocysteine analogues
    • Serafinowski, P. Synthesis of some S-3'-deoxyadenosyl-L-homocysteine analogues. Nucleic Acids Res., 1987, 15(3), 1121-1137.
    • (1987) Nucleic Acids Res , vol.15 , Issue.3 , pp. 1121-1137
    • Serafinowski, P.1
  • 233
    • 0023780763 scopus 로고
    • Synthesis of the dideoxynucleosides ddC and CNT from glutamic acid, ribonolactone, and pyrimidine bases
    • Okabe, M.; Sun, R.-C.; Tam, S. Y.-K.; Todaro, L. J.; Coffen, D. L. Synthesis of the dideoxynucleosides ddC and CNT from glutamic acid, ribonolactone, and pyrimidine bases. J. Org. Chem., 1988, 53(20), 4780-4786.
    • (1988) J. Org. Chem. , vol.53 , Issue.20 , pp. 4780-4786
    • Okabe, M.1    Sun, R.-C.2    Tam, S.Y.-K.3    Todaro, L.J.4    Coffen, D.L.5
  • 234
    • 0024997489 scopus 로고
    • Synthesis of 3-deaza-2'-deoxyadenosine and 3-deaza-2',3'-dideoxyadenosine: Glycosylation of the 4-chloroimidazo[4,5-c]pyridinyl anion
    • Seela, F.; Rosemeyer, H.; Fischer, S. Synthesis of 3-deaza-2'-deoxyadenosine and 3-deaza-2',3'-dideoxyadenosine: glycosylation of the 4-chloroimidazo[4,5-c]pyridinyl anion. Helv. Chim. Acta, 1990, 73(6), 1602-1611.
    • (1990) Helv. Chim. Acta. , vol.73 , Issue.6 , pp. 1602-1611
    • Seela, F.1    Rosemeyer, H.2    Fischer, S.3
  • 235
    • 0025829398 scopus 로고
    • Syntheses of pyrrolo[2,3-d]pyrimidine 2',3'-dideoxyribonucleosides related to 2',3'-dideoxyadenosine and 2',3'-dideoxyguanosine and inhibitory activity of 5'-triphosphates on HIV-1 reverse transcriptase
    • Seela, F.; Muth, H.-P.; Röling, A. Syntheses of pyrrolo[2,3-d]pyrimidine 2',3'-dideoxyribonucleosides related to 2',3'-dideoxyadenosine and 2',3'-dideoxyguanosine and inhibitory activity of 5'-triphosphates on HIV-1 reverse transcriptase. Helv. Chim. Acta, 1991, 74(3), 554-564.
    • (1991) Helv. Chim. Acta. , vol.74 , Issue.3 , pp. 554-564
    • Seela, F.1    Muth, H.-P.2    Röling, A.3
  • 236
    • 33847752738 scopus 로고
    • Facile synthesis of pyrrolo[2,3-d]pyrimidine and pyrrolo[3,2-c]pyridine 2',3'-dideoxyribonucleosides via nucleobase anion glycosylation with 2,3-dideoxy-D-glyceropentofuranosyl chloride
    • Seela, F.; Bourgeois, W.; Muth, H.-P.; Rosemeyer, H. Facile synthesis of pyrrolo[2,3-d]pyrimidine and pyrrolo[3,2-c]pyridine 2',3'-dideoxyribonucleosides via nucleobase anion glycosylation with 2,3-dideoxy-D-glyceropentofuranosyl chloride. Heterocycles, 1989 29(11), 2193-2197.
    • (1989) Heterocycles , vol.29 , Issue.11 , pp. 2193-2197
    • Seela, F.1    Bourgeois, W.2    Muth, H.-P.3    Rosemeyer, H.4
  • 237
    • 84982373258 scopus 로고
    • Tertiary phosphane/tetrachloromethane, a versatile reagent for chlorination, dehydration, and P-N linkage
    • Appel, R. Tertiary phosphane/tetrachloromethane, a versatile reagent for chlorination, dehydration, and P-N linkage. Angew. Chem. Int. Ed., 1975, 14(12), 801-811.
    • (1975) Angew. Chem. Int. Ed. , vol.14 , Issue.12 , pp. 801-811
    • Appel, R.1
  • 238
    • 0001072616 scopus 로고
    • Stereoselective preparations of ribofuranosyl chlorides and ribofuranosyl acetates. Solvent effects and stereoselectivity in the reaction of ribofuranosyl acetates with trimethylallylsilane
    • Wilcox, C. S.; Otoski, R. M. Stereoselective preparations of ribofuranosyl chlorides and ribofuranosyl acetates. Solvent effects and stereoselectivity in the reaction of ribofuranosyl acetates with trimethylallylsilane. Tetrahedron Lett., 1986, 27(9), 1011-1014.
    • (1986) Tetrahedron Lett , vol.27 , Issue.9 , pp. 1011-1014
    • Wilcox, C.S.1    Otoski, R.M.2
  • 240
    • 0023124801 scopus 로고
    • Both 2',3'-dideoxythymidine and its 2',3'-unsaturated derivative (2',3'-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro
    • Baba, M.; Pauwels, R.; Herdewijn, P.; De Clercq, E.; Desmyter, J.; Vandeputte, M. Both 2',3'-dideoxythymidine and its 2',3'-unsaturated derivative (2',3'-dideoxythymidinene) are potent and selective inhibitors of human immunodeficiency virus replication in vitro. Biochem. Biophys. Res. Commun., 1987, 142(1), 128-134.
    • (1987) Biochem. Biophys. Res. Commun. , vol.142 , Issue.1 , pp. 128-134
    • Baba, M.1    Pauwels, R.2    Herdewijn, P.3    de Clercq, E.4    Desmyter, J.5    Vandeputte, M.6
  • 242
    • 0027231474 scopus 로고
    • Stimulation of rat liver glycogen synthesis by the adenosine kinase inhibitor 5-iodotubercidin
    • Flückiger-Isler, R. E.; Walter, P. Stimulation of rat liver glycogen synthesis by the adenosine kinase inhibitor 5-iodotubercidin. Biochem. J., 1993, 292, 85-91.
    • (1993) Biochem. J. , vol.292 , pp. 85-91
    • Flückiger-Isler, R.E.1    Walter, P.2
  • 243
    • 0028220187 scopus 로고
    • Identification of the glycogenic compound 5-iodotubercidin as a general protein kinase inhibitor
    • Massillon, D.; Stalmans, W.; van de Werve, G.; Bollen, M. Identification of the glycogenic compound 5-iodotubercidin as a general protein kinase inhibitor. Biochem. J., 1994, 299, 123-128.
    • (1994) Biochem. J. , vol.299 , pp. 123-128
    • Massillon, D.1    Stalmans, W.2    van de Werve, G.3    Bollen, M.4
  • 244
    • 0000455364 scopus 로고
    • Synthesis of L-ribofuranose and Ladenosine
    • Acton, E. M.; Ryan, K. J.; Goodman, L. Synthesis of L-ribofuranose and Ladenosine. J. Am. Chem. Soc., 1964, 86(23), 5352-5354.
    • (1964) J. Am. Chem. Soc. , vol.86 , Issue.23 , pp. 5352-5354
    • Acton, E.M.1    Ryan, K.J.2    Goodman, L.3
  • 245
    • 0014189266 scopus 로고
    • Studies on synthetic nucleotides. IV. Preparation of L-β-ribonucleosides and L-β-ribonucleotides
    • Asai, M.; Hieda, H.; Shimizu, B. Studies on synthetic nucleotides. IV. Preparation of L-β-ribonucleosides and L-β-ribonucleotides. Chem. Pharm. Bull., 1967, 15(12), 1863-1870.
    • (1967) Chem. Pharm. Bull. , vol.15 , Issue.12 , pp. 1863-1870
    • Asai, M.1    Hieda, H.2    Shimizu, B.3
  • 246
    • 0000016897 scopus 로고
    • Preparation of some O-L-ribonucleosides
    • Holý A.; Šorm, F. Preparation of some O-L-ribonucleosides. Collect. Czech. Chem. Commun., 1969, 34, 3383-3401.
    • (1969) Collect. Czech. Chem. Commun. , vol.34 , pp. 3383-3401
    • Holý, A.1    Šorm, F.2
  • 247
    • 0032403491 scopus 로고    scopus 로고
    • Recent advances in Lnucleosides: Chemistry and biology
    • Wang, P.; Hong, J. H.; Cooperwood, J. S.; Chu, C. K. Recent advances in Lnucleosides: chemistry and biology. Antiviral Res., 1998, 40, 19-44.
    • (1998) Antiviral Res , vol.40 , pp. 19-44
    • Wang, P.1    Hong, J.H.2    Cooperwood, J.S.3    Chu, C.K.4
  • 248
    • 0035822541 scopus 로고    scopus 로고
    • L-Nucleosides as chemotherapeutic agents
    • Gumina, G.; Song, G.-Y.; Chu, C. K. L-Nucleosides as chemotherapeutic agents. FEMS Microbiol. Lett., 2001, 202(1), 9-15.
    • (2001) FEMS Microbiol. Lett. , vol.202 , Issue.1 , pp. 9-15
    • Gumina, G.1    Song, G.-Y.2    Chu, C.K.3
  • 252
    • 0034026483 scopus 로고    scopus 로고
    • Enantioselectivity of the antiviral effects of nucleoside analogues
    • Zemlicka, J. Enantioselectivity of the antiviral effects of nucleoside analogues. Pharmacol. Ther., 2000, 85(3), 251-266.
    • (2000) Pharmacol. Ther. , vol.85 , Issue.3 , pp. 251-266
    • Zemlicka, J.1
  • 254
    • 0030846114 scopus 로고    scopus 로고
    • Convenient preparation of 2-deoxy-3,5-di-O-p-toluoyl-β-D-erythro-pentofuranosyl chloride
    • Rolland, V.; Kotera, M.; Lhomme, J. Convenient preparation of 2-deoxy-3,5-di-O-p-toluoyl-β-D-erythro-pentofuranosyl chloride. Synth. Commun., 1997, 27(20), 3505-3511.
    • (1997) Synth. Commun. , vol.27 , Issue.20 , pp. 3505-3511
    • Rolland, V.1    Kotera, M.2    Lhomme, J.3
  • 255
    • 33748329052 scopus 로고    scopus 로고
    • Pyrrolo[2,3-d]pyrimidine β-L-nucleosides containing 7-deazaadenine, 2-amino-7-deazaadenine, 7-deazaguanine, 7-deazaisoguanine, and 7-deazaxanthine
    • Seela, F.; Peng, X. Pyrrolo[2,3-d]pyrimidine β-L-nucleosides containing 7-deazaadenine, 2-amino-7-deazaadenine, 7-deazaguanine, 7-deazaisoguanine, and 7-deazaxanthine. Collect. Czech. Chem. Commun., 2006, 71, 956-977.
    • (2006) Collect. Czech. Chem. Commun. , vol.71 , pp. 956-977
    • Seela, F.1    Peng, X.2
  • 256
    • 31144466345 scopus 로고    scopus 로고
    • 7-Functionalized 7-deazapurine ribonucleosides related to 2-aminoadenosine, guanosine, and xanthosine: Glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose
    • F.; Peng, X. 7-Functionalized 7-deazapurine ribonucleosides related to 2-aminoadenosine, guanosine, and xanthosine: glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose. J. Org. Chem., 2006, 71(1), 81-90.
    • (2006) J. Org. Chem. , vol.71 , Issue.1 , pp. 81-90
  • 257
    • 0025143181 scopus 로고
    • Direct C-glycosylation of guanine analogs: The synthesis and antiviral activity of certain 7- and 9-deazaguanine C-nucleosides
    • Girgis, N. S.; Michael, M. A.; Smee, D. F.; Alaghamandan, H. A.; Robins, R. K.; Cottam, H. B. Direct C-glycosylation of guanine analogs: the synthesis and antiviral activity of certain 7- and 9-deazaguanine C-nucleosides. J. Med. Chem., 1990, 33(10), 2750-2755.
    • (1990) J. Med. Chem. , vol.33 , Issue.10 , pp. 2750-2755
    • Girgis, N.S.1    Michael, M.A.2    Smee, D.F.3    Alaghamandan, H.A.4    Robins, R.K.5    Cottam, H.B.6
  • 258
    • 0035906483 scopus 로고    scopus 로고
    • The C8-(2'-deoxy-β-D-ribofuranoside) of 7-deazaguanine: Synthesis and base pairing of oligonucleotides with unusually linked nucleobases
    • Seela, F.; Debelak, H. The C8-(2'-deoxy-β-D-ribofuranoside) of 7-deazaguanine: synthesis and base pairing of oligonucleotides with unusually linked nucleobases. J. Org. Chem., 2001, 66(10), 3303-3312.
    • (2001) J. Org. Chem. , vol.66 , Issue.10 , pp. 3303-3312
    • Seela, F.1    Debelak, H.2
  • 259
    • 0001518039 scopus 로고
    • Transient protection: Efficient oneflask syntheses of protected deoxynucleosides
    • Ti, G. S.; Gaffney, B. L.; Jones, R. A. Transient protection: efficient oneflask syntheses of protected deoxynucleosides. J. Am. Chem. Soc., 1982, 104(5), 1316-1319.
    • (1982) J. Am. Chem. Soc. , vol.104 , Issue.5 , pp. 1316-1319
    • Ti, G.S.1    Gaffney, B.L.2    Jones, R.A.3
  • 260
    • 0000684310 scopus 로고
    • Synthesis of dodecadeoxyribonucleotides containing a pyrrolo[2,3-d]pyrimidine nucleoside and their base-pairing ability
    • Inoue, H.; Imura, A.; Ohtsuka, E. Synthesis of dodecadeoxyribonucleotides containing a pyrrolo[2,3-d]pyrimidine nucleoside and their base-pairing ability. Nippon Kagaku Kaishi, 1987, 7, 1214-1220.
    • (1987) Nippon Kagaku Kaishi , vol.7 , pp. 1214-1220
    • Inoue, H.1    Imura, A.2    Ohtsuka, E.3
  • 261
    • 0029945838 scopus 로고    scopus 로고
    • G/C-modified oligodeoxynucleotides with selective complementarity: Synthesis and hybridization properties
    • Woo, J.; Meyer, Jr., R. B.; Gamper, H. B. G/C-modified oligodeoxynucleotides with selective complementarity: synthesis and hybridization properties. Nucleic Acids Res., 1996, 24(13), 2470-2475.
    • (1996) Nucleic Acids Res , vol.24 , Issue.13 , pp. 2470-2475
    • Woo, J.1    Meyer, R.B.2    Gamper, H.B.3
  • 262
    • 37049091729 scopus 로고
    • The synthesis of nucleosides derived from 5-ethynyluracil and 5-ethynylcytosine
    • Barr, P. J.; Jones, A. S.; Serafinowski, P.; Walker, R. T. The synthesis of nucleosides derived from 5-ethynyluracil and 5-ethynylcytosine. J. Chem. Soc., Perkin Trans. 1, 1978, 1263-1267.
    • (1978) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1263-1267
    • Barr, P.J.1    Jones, A.S.2    Serafinowski, P.3    Walker, R.T.4
  • 263
    • 27544440920 scopus 로고
    • Nucleic acid related compounds. 39. Efficient conversion of 5-iodo to 5-alkynyl and derived 5-substituted uracil bases and nucleosides
    • Robins, M. J.; Barr, P. J. Nucleic acid related compounds. 39. Efficient conversion of 5-iodo to 5-alkynyl and derived 5-substituted uracil bases and nucleosides. J. Org. Chem., 1983, 48(11), 1854-1862.
    • (1983) J. Org. Chem. , vol.48 , Issue.11 , pp. 1854-1862
    • Robins, M.J.1    Barr, P.J.2
  • 265
    • 42349083343 scopus 로고    scopus 로고
    • Pyrrolo-dC oligonucleotides bearing alkynyl side chains with terminal triple bonds: Synthesis, base pairing and fluorescent dye conjugates prepared by the azide-alkyne click reaction
    • Seela, F.; Sirivolu, V. R. Pyrrolo-dC oligonucleotides bearing alkynyl side chains with terminal triple bonds: synthesis, base pairing and fluorescent dye conjugates prepared by the azide-alkyne click reaction. Org. Biomol. Chem., 2008, 6(9), 1674-1687.
    • (2008) Org. Biomol. Chem. , vol.6 , Issue.9 , pp. 1674-1687
    • Seela, F.1    Sirivolu, V.R.2
  • 266
    • 1242338125 scopus 로고    scopus 로고
    • Pyrrolo-dC and pyrrolo-C: Fluorescent analogs of cytidine and 2'-deoxycytidine for the study of oligonucleotides
    • Berry, D. A.; Jung, K.-Y.; Wise, D. S.; Sercel, A. D.; Pearson, W. H.; Mackie, H.; Randolph, J. B.; Somers, R. L. Pyrrolo-dC and pyrrolo-C: fluorescent analogs of cytidine and 2'-deoxycytidine for the study of oligonucleotides. Tetrahedron Lett., 2004, 45(11), 2457-2461.
    • (2004) Tetrahedron Lett , vol.45 , Issue.11 , pp. 2457-2461
    • Berry, D.A.1    Jung, K.-Y.2    Wise, D.S.3    Sercel, A.D.4    Pearson, W.H.5    Mackie, H.6    Randolph, J.B.7    Somers, R.L.8
  • 267
    • 0038352367 scopus 로고    scopus 로고
    • Synthesis and some biochemical properties of a novel 5,6,7,8-tetrahydropyrimido[4,5-c]pyridazine nucleoside
    • Loakes, D.; Brown, D. M.; Salisbury, S. A.; McDougall, M. G.; Neagu, C.; Nampalli, S.; Kumar, S. Synthesis and some biochemical properties of a novel 5,6,7,8-tetrahydropyrimido[4,5-c]pyridazine nucleoside. Helv. Chim. Acta, 2003, 86(4), 1193-1204.
    • (2003) Helv. Chim. Acta. , vol.86 , Issue.4 , pp. 1193-1204
    • Loakes, D.1    Brown, D.M.2    Salisbury, S.A.3    McDougall, M.G.4    Neagu, C.5    Nampalli, S.6    Kumar, S.7
  • 268
    • 30444456685 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 6-(alkyn-1-yl)furo[2,3-d] pyrimidin-2(3H)-one base and nucleoside derivatives
    • Robins, M. J.; Miranda, K.; Rajwanshi, V. K.; Peterson, M. A.; Andrei, G.; Snoeck, R.; De Clercq, E.; Balzarini, J. Synthesis and biological evaluation of 6-(alkyn-1-yl)furo[2,3-d] pyrimidin-2(3H)-one base and nucleoside derivatives. J. Med. Chem., 2005, 49(1), 391-398.
    • (2005) J. Med. Chem. , vol.49 , Issue.1 , pp. 391-398
    • Robins, M.J.1    Miranda, K.2    Rajwanshi, V.K.3    Peterson, M.A.4    Andrei, G.5    Snoeck, R.6    de Clercq, E.7    Balzarini, J.8
  • 269
    • 0035847684 scopus 로고    scopus 로고
    • Bicyclic nucleoside inhibitors of varicella-zoster virus (VZV): The effect of terminal unsaturation in the side chain
    • Srinivasan, S.; McGuigan, C.; Andrei, G.; Snoeck, R.; De Clercq, E.; Balzarini, J. Bicyclic nucleoside inhibitors of varicella-zoster virus (VZV): the effect of terminal unsaturation in the side chain. Biorg. Med. Chem. Lett., 2001, 11(3), 391-393.
    • (2001) Biorg. Med. Chem. Lett. , vol.11 , Issue.3 , pp. 391-393
    • Srinivasan, S.1    McGuigan, C.2    Andrei, G.3    Snoeck, R.4    de Clercq, E.5    Balzarini, J.6
  • 270
    • 34547855101 scopus 로고    scopus 로고
    • Design and evaluation of a potential mutagen for Hepatitis C virus
    • Koh, Y.-H.; Shim, J. H.; Girardet, J.-L.; Hong, Z. Design and evaluation of a potential mutagen for Hepatitis C virus. Biorg. Med. Chem. Lett., 2007, 17(18), 5261-5264.
    • (2007) Biorg. Med. Chem. Lett. , vol.17 , Issue.18 , pp. 5261-5264
    • Koh, Y.-H.1    Shim, J.H.2    Girardet, J.-L.3    Hong, Z.4
  • 271
    • 69949141591 scopus 로고    scopus 로고
    • Studies on the glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-Obenzoyl-β-D-ribofuranose: The formation of regioisomers during toyocamycin and 7-deazainosine syntheses
    • Leonard, P.; Ingale, S. A.; Ding, P.; Ming, X.; Seela, F. Studies on the glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-Obenzoyl-β-D-ribofuranose: the formation of regioisomers during toyocamycin and 7-deazainosine syntheses. Nucleosides Nucleotides Nucleic Acids, 2009, 28(5), 678-694.
    • (2009) Nucleosides Nucleotides Nucleic Acids , vol.28 , Issue.5 , pp. 678-694
    • Leonard, P.1    Ingale, S.A.2    Ding, P.3    Ming, X.4    Seela, F.5
  • 272
    • 57649089169 scopus 로고    scopus 로고
    • Ends free and self-quenched molecular beacon with pyrene labeled pyrrolocytidine in the middle of the stem
    • Saito, Y.; Shinohara, Y.; Bag, S. S.; Takeuchi, Y.; Matsumoto, K.; Saito, I. Ends free and self-quenched molecular beacon with pyrene labeled pyrrolocytidine in the middle of the stem. Tetrahedron, 2009, 65(4), 934-939.
    • (2009) Tetrahedron , vol.65 , Issue.4 , pp. 934-939
    • Saito, Y.1    Shinohara, Y.2    Bag, S.S.3    Takeuchi, Y.4    Matsumoto, K.5    Saito, I.6
  • 273
    • 34247253265 scopus 로고    scopus 로고
    • Selective fluorometric detection of guanosine-containing sequences by 6-phenylpyrrolocytidine in DNA
    • Hudson, R. H. E.; Ghorbani-Choghamarani, A. Selective fluorometric detection of guanosine-containing sequences by 6-phenylpyrrolocytidine in DNA. Synlett, 2007, 870-873.
    • (2007) Synlett , pp. 870-873
    • Hudson, R.H.E.1    Ghorbani-Choghamarani, A.2
  • 274
    • 36949031273 scopus 로고    scopus 로고
    • The 6-methoxymethyl derivative of pyrrolo-dC for selective fluorometric detection of guanosine-containing sequences
    • Hudson, R. H. E.; Choghamarani, A. G. The 6-methoxymethyl derivative of pyrrolo-dC for selective fluorometric detection of guanosine-containing sequences. Nucleosides Nucleotides Nucleic Acids, 2007, 26(6), 533-537.
    • (2007) Nucleosides Nucleotides Nucleic Acids , vol.26 , Issue.6 , pp. 533-537
    • Hudson, R.H.E.1    Choghamarani, A.G.2
  • 275
    • 8644219601 scopus 로고    scopus 로고
    • 3-catalyzed preparation of substituted furanopyrimidine nucleosides
    • Aucagne, V.; Amblard, F.; Agrofoglio, L. A. Highly efficient AgNO3-catalyzed preparation of substituted furanopyrimidine nucleosides. Synlett, 2004, 2406-2408.
    • (2004) Synlett , pp. 2406-2408
    • Aucagne, V.1    Amblard, F.2    Agrofoglio, L.A.3
  • 276
    • 20444469710 scopus 로고    scopus 로고
    • Recognition of CG inversions in DNA triple helices by methylated 3Hpyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues
    • Ranasinghe, R. T.; Rusling, D. A.; Powers, V. E. C.; Fox, K. R.; Brown, T. Recognition of CG inversions in DNA triple helices by methylated 3Hpyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues. Chem. Commun., 2005, 2555-2557.
    • (2005) Chem. Commun. , pp. 2555-2557
    • Ranasinghe, R.T.1    Rusling, D.A.2    Powers, V.E.C.3    Fox, K.R.4    Brown, T.5
  • 277
    • 0035804928 scopus 로고    scopus 로고
    • Fluorescence characterization of the transcription bubble in elongation complexes of T7 RNA polymerase
    • Liu, C.; Martin, C. T. Fluorescence characterization of the transcription bubble in elongation complexes of T7 RNA polymerase. J. Mol. Biol., 2001, 308(3), 465-475.
    • (2001) J. Mol. Biol. , vol.308 , Issue.3 , pp. 465-475
    • Liu, C.1    Martin, C.T.2
  • 278
    • 0032569181 scopus 로고    scopus 로고
    • A cytosine analogue capable of clamp-like binding to a guanine in helical nucleic acids
    • Lin, K.-Y.; Matteucci, M. D. A cytosine analogue capable of clamp-like binding to a guanine in helical nucleic acids. J. Am. Chem. Soc., 1998, 120(33), 8531-8532.
    • (1998) J. Am. Chem. Soc. , vol.120 , Issue.33 , pp. 8531-8532
    • Lin, K.-Y.1    Matteucci, M.D.2
  • 280
    • 36949008769 scopus 로고    scopus 로고
    • CG Base pair recognition within DNA triple helices using N-methyl-3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues
    • Gerrard, S. R.; Srinivasan, N.; Fox, K. R.; Brown, T. CG Base pair recognition within DNA triple helices using N-methyl-3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues. Nucleosides Nucleotides Nucleic Acids, 2007, 26(10), 1363-1367.
    • (2007) Nucleosides Nucleotides Nucleic Acids , vol.26 , Issue.10 , pp. 1363-1367
    • Gerrard, S.R.1    Srinivasan, N.2    Fox, K.R.3    Brown, T.4
  • 281
    • 78049345254 scopus 로고    scopus 로고
    • CG base pair recognition within DNA triple helices by modified N-methylpyrrolo-dC nucleosides
    • Gerrard, S. R.; Edrees, M. M.; Bouamaied, I.; Fox, K. R.; Brown, T. CG base pair recognition within DNA triple helices by modified N-methylpyrrolo-dC nucleosides. Org. Biomol. Chem., 2010, 8(22), 5087-5096.
    • (2010) Org. Biomol. Chem. , vol.8 , Issue.22 , pp. 5087-5096
    • Gerrard, S.R.1    Edrees, M.M.2    Bouamaied, I.3    Fox, K.R.4    Brown, T.5
  • 282
    • 0028908575 scopus 로고
    • Tricyclic 2'-deoxycytidine analogs: Syntheses and incorporation into oligodeoxynucleotides which have enhanced binding to complementary RNA
    • Lin, K.-Y.; Jones, R. J.; Matteucci, M. Tricyclic 2'-deoxycytidine analogs: syntheses and incorporation into oligodeoxynucleotides which have enhanced binding to complementary RNA. J. Am. Chem. Soc., 1995, 117(13), 3873-3874.
    • (1995) J. Am. Chem. Soc. , vol.117 , Issue.13 , pp. 3873-3874
    • Lin, K.-Y.1    Jones, R.J.2    Matteucci, M.3
  • 283
    • 0037078836 scopus 로고    scopus 로고
    • Synthesis of amino- and guanidino-G-clamp PNA monomers
    • Ausín, C.; Ortega, J.-A.; Robles, J.; Grandas, A.; Pedroso, E. Synthesis of amino- and guanidino-G-clamp PNA monomers. Org. Lett., 2002, 4(23), 4073-4075.
    • (2002) Org. Lett. , vol.4 , Issue.23 , pp. 4073-4075
    • Ausín, C.1    Ortega, J.-A.2    Robles, J.3    Grandas, A.4    Pedroso, E.5
  • 285
    • 0038268062 scopus 로고    scopus 로고
    • Steric inhibition of human immunodeficiency virus type-1 Tat-dependent trans-activation in vitro and in cells by oligonucleotides containing 2β-O-methyl G-clamp ribonucleoside analogues
    • Holmes, S. C.; Arzumanov, A. A.; Gait, M. J. Steric inhibition of human immunodeficiency virus type-1 Tat-dependent trans-activation in vitro and in cells by oligonucleotides containing 2β-O-methyl G-clamp ribonucleoside analogues. Nucleic Acids Res., 2003, 31(11), 2759-2768.
    • (2003) Nucleic Acids Res , vol.31 , Issue.11 , pp. 2759-2768
    • Holmes, S.C.1    Arzumanov, A.A.2    Gait, M.J.3
  • 286
    • 1542789868 scopus 로고    scopus 로고
    • 7-Deazaisoguanine quartets: Self-assembled oligonucleotides lacking the Hoogsteen motif
    • Seela, F.; Wei, C. 7-Deazaisoguanine quartets: self-assembled oligonucleotides lacking the Hoogsteen motif. Chem. Commun., 1997, 1869-1870.
    • (1997) Chem. Commun. , pp. 1869-1870
    • Seela, F.1    Wei, C.2
  • 288
    • 0035213433 scopus 로고    scopus 로고
    • Quadruplex and pentaplex self-assemblies of oligonucleotides containing short runs of 8-aza-7-deaza-2'-deoxyisoguanosine or 2'-deoxyisoguanosine
    • Seela, F.; Kröschel, R. Quadruplex and pentaplex self-assemblies of oligonucleotides containing short runs of 8-aza-7-deaza-2'-deoxyisoguanosine or 2'-deoxyisoguanosine. Bioconjugate Chem., 2001, 12(6), 1043-1050.
    • (2001) Bioconjugate Chem , vol.12 , Issue.6 , pp. 1043-1050
    • Seela, F.1    Kröschel, R.2
  • 289
    • 0026494947 scopus 로고
    • A dideazatetrahydrofolate analog lacking a chiral center at C-6, N-[4-[2-(2-amino-3,4-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-L-glutamic acid, is an inhibitor of thymidylate synthase
    • Taylor, E. C.; Kuhnt, D.; Shih, C.; Rinzel, S. M.; Grindey, G. B.; Barredo, J.; Jannatipour, M.; Moran, R. G. A dideazatetrahydrofolate analog lacking a chiral center at C-6, N-[4-[2-(2-amino-3,4-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-L-glutamic acid, is an inhibitor of thymidylate synthase. J. Med. Chem., 1992, 35(23), 4450-4454.
    • (1992) J. Med. Chem. , vol.35 , Issue.23 , pp. 4450-4454
    • Taylor, E.C.1    Kuhnt, D.2    Shih, C.3    Rinzel, S.M.4    Grindey, G.B.5    Barredo, J.6    Jannatipour, M.7    Moran, R.G.8
  • 290
    • 67650468760 scopus 로고    scopus 로고
    • Sequence-independent and rapid long-range charge transfer through DNA
    • Kawai, K.; Kodera, H.; Osakada, Y.; Majima, T. Sequence-independent and rapid long-range charge transfer through DNA. Nat. Chem., 2009, 1(2), 156-159.
    • (2009) Nat. Chem. , vol.1 , Issue.2 , pp. 156-159
    • Kawai, K.1    Kodera, H.2    Osakada, Y.3    Majima, T.4


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