Синтез мономеров полиамидных миметиков нуклеиновых кислот и исследование их свойств, страница 19
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– 1st ed. – P. 847-880.76.Porcheddu A., Giacomelli G., Piredda I., Carta M., Nieddu G. A Practical and EfficientApproach to PNA Monomers Compatible with Fmoc-Mediated Solid-Phase Synthesis Protocols.// Eur. J. Org. Chem. – 2008. – P. 5786–5797.77.Christensen L., Fitzpatrick R., Gildea B., Petersen K. H., Hansen H. F., Koch T., EgholmM., Buchardt O., Nielsen P. E., Coull J., Berg, R.
H. Solid-phase synthesis of peptide nucleicacids. // J. Pept. Sci. – 1995. – V. 1(3). – P. 175-183.78.Joshi R., Jha D., Su W., Engelmann J. Facile synthesis of peptide nucleic acids andpeptide nucleic acid-peptide conjugates on an automated peptide synthesizer. // J. Pept.
Sci. –2011. – V. 17. – P. 8-13.79.Dragulescu-Andrasi A., Rapireddy S., Frezza B. M., Gayathri C., Gil R. R., Ly D. H. Asimple γ-backbone modification preorganizes peptide nucleic acid into a helical structure. // J.Am. Chem. – 2006. – V. 128. – P. 10258-10267.80.Zhou P., Dragulescu-Andrasi A., Bhattacharya B., O’Keefe H., Vatta P., Hyldig-NielsenJ. J., Ly D. H. Synthesis of cell-permeable peptide nucleic acids and characterization of theirhybridization and uptake properties. // Bioorg. Med. Chem.
Lett. – 2006. – V. 16. – P. 49314935.9481.Haaima G., Lohse A., Buchardt O., Nielsen P. E. Peptide Nucleic Acids (PNAs)Containing Thymine Monomers Derived from Chiral Amino Acids: Hybridization and SolubilityProperties of D-Lysine PNA. // Angew. Chem. Int. Ed. – 1996. – V. 35(17). – P. 1939-1942.82.Zarra R., Montesarchio D., Coppola C., Bifulco G., Di Micco S., Izzo I., De Riccardis F.Design, Synthesis, and Hybridisation of Water-Soluble, Peptoid Nucleic Acid Oligomers Taggedwith Thymine. // Eur.
J. Org. Chem. – 2009. – P. 6113-6120.83.De Cola C., Manicardi A., Corradini R., Izzo I., De Riccardis F. Carboxyalkyl peptoidPNAs: synthesis and hybridization properties. // Tetrahedron. – 2012. – V. 68. – P. 499-506.84.Efimov V. A., Choob M. V., Buryakova A. A., Chakhmakhcheva O. G. Synthesis AndBinding Study Of Phosphonate Analogues Of Pnas And Their Hybrids With Pnas. // Nucleosides& Nucleotides. – 1998. – V. 17(9-11). – P. 1671-1679.85.Efimov V. A., Chakhmakhcheva O. G., Wickstrom E.
Synthesis and Application ofNegatively Charged PNA Analogues. // Nucleosides, Nucleotides & Nucleic Acids. – 2005. – V.24. – P. 1853-1874.86.Shiraishi T., Hamzavi R., Nielsen P. E. Subnanomolar antisense activity of phosphonate-peptide nucleic acid (PNA) conjugates delivered by cationic lipids to HeLa cells. // NucleicAcids Research. – 2008. – V. 36(13). – P. 4424-4432.87.Avitabile C., Moggio L., Malgieri G., Capasso D., Di Gaetano S., Saviano M., Pedone C.,Romanelli A. γ-sulphate PNA (PNA S): Highly Selective DNA Binding Molecule ShowingPromising Antigene Activity.
// PLoS ONE. – 2012. – V. 7(5). – e35774. – P. 1-10.88.Tilani N., De Costa S., Heemstra J. M. Evaluating the Effect of Ionic Strength on DuplexStability for PNA Having Negatively or Positively Charged Side Chains. // PLoS ONE. – 2013. –V. 8(3). – e58670. – P. 1-8.89.Nielsen P. E. Modulating Gene Function with Peptide Nucleic Acids (PNA). In Antisensedrug technology: principles, strategies, and applications. // ed. S. T. Crooke, CRC Press. – 2008.– 2nd ed. – P. 507-518.90.Sazani P., Gemignani F., Kang S.-H., Maier M.
A., Manoharan M., Persmark M., BortnerD., Kole R. Systemically delivered antisense oligomers upregulate gene expression in mousetissues. // Nature Biotech. – 2002. – V. 20. – P. 1228-1233.91.Hamzavi R., Dolle F., Tavitian B., Dahl O., Nielsen P. E. Modulation of thePharmacokinetic Properties of PNA: Preparation of Galactosyl, Mannosyl, Fucosyl, NAcetylgalactosaminyl, and N-Acetylglucosaminyl Derivatives of Aminoethylglycine PeptideNucleic Acid Monomers and Their Incorporation into PNA Oligomers.
// Bioconjugate Chem. –2003. – V. 14. – P. 941-954.9592.Upadhyay A., Ponzio N. M., Pandey V. N. Immunological Response to Peptide NucleicAcid and its Peptide Conjugate Targeted to Transactivation Response (TAR) Region of HIV-1RNA Genome. // Oigonucleotides. – 2008. – V. 18. – P. 329-335.93.Sheng L., Miao C., JinDu L, HaoBo Z., JinQing W, ShengRong Y. Application ofpeptide nucleic acids containing azobenzene self-assembled electrochemical biosensors indetecting DNA sequences. // Sci. China Ser. B-Chem. – 2009.
– V. 52(7). – P. 1009-1013.94.Galbiati S., Foglieni B., Travi M., Curcio C., Restagno G., Sbaiz L., Smid M., Pasi F.,Ferrari A., Ferrari M., Cremonesi L. Peptide-nucleic acid-mediated enriched polymerase chainreaction as a key point for non-invasive prenatal diagnosis of β-thalassemia.
// Haematologica. –2008. – V. 93(4). – P. 610-614.95.Choi J.-J., Cho M., Oh M., Kim H., Kil M.-S., Park H. PNA-mediated Real-Time PCRClamping for Detection of EGFR Mutations. // Bull. Korean Chem. Soc. – 2010. – V. 31(12). –P. 3525-3529.96.Lusvarghi S., Murphy C. T., Roy S., Tanious F. A., Sacui I., Wilson W. D., Ly D. H.,Armitage B. A. Loop and Backbone Modifications of Peptide Nucleic Acid Improve GQuadruplex Binding Selectivity. // J.
Am. Chem. Soc. – 2009. – 131. – P. 18415-18424.97.Boyarskaya N. P., Prokhorov D. I., Kirillova Yu. G., Zvonkova E. N., Shvets V. I.Synthesis of protected pseudopeptides from dicarboxylic amino acids by Mitsunobucondensation. // Tetrahedron Letters. –2005. – V. 46. – P. 7359-7362.98.Thomson S. A., Josey J. A., Cadilla R., Gaul M. D., Hassman C. F., Luzzio M. J., Pipe A.J., Reed K. L., Ricca D. J., Wiethe R.
W., Noble S. A. Fmoc Mediated Synthesis of PeptideNucleic Acids. // Tetrahedron. – 1995. – V. 51(22). – P. 6179-6194.99.Will D. W., Breipohl G., Langner D., Knolle J., Uhlmann E. The Synthesis of PolyamideNucleic Acids using a Novel Monomethoxytrityl Protecting-Group Strategy. // Tetrahedron. –1995.
– V. 51(44). – P. 12069-12082.100.Timár Z., Kovács L., Kovács G., Schmél Z. Fmoc/Acyl protecting groups in the synthesisof polyamide (peptide) nucleic acid monomers. // J. Chem. Soc. Perkin Trans. – 2000. – V. 1. –P. 19-26.101.Perrin D. D., Armarego W. L. F. Purification of organic chemicals. In purification oflaboratory chemicals. // Pergamon Press. – 1988. – 3rd ed. – P. 65-310.102.Liu X., Zheng, Q.-H., Hutchins G.
D., Fei X., Erickson L. C., Miller K. D., Mock B. H.,Glick-Wilson B. E., Winkle W. L., Stone K. L., Carlson K. A. A Convenient Procedure for theSynthesis of O6-Benzylguanine Derivatives by Phase Transfer Catalysis. // Synth. Comm. –2003. – V. 33(6). – P. 941-952.96103.Dolan M.
E., Moschel R. C., Pegg A. E. Depletion of mammalian O6-alkylguanine-DNAalkyltransferase activity by O6-benzylguanine provides a means to evaluate the role of thisprotein in protection against carcinogenic and therapeutic alkylating agents. // Proc. Natl. Acad.Sci.
USA. – 1990. – V. 87. – P. 5368-5372.104.Barth C., Seitz O., Kunz H. Synthese von 6-O-Benzylguanin und seinen Anker-Konjugaten. // Z. Naturforsch. – 2004. – V. 59b. – P. 802-806.105.Деженков А. В., Прохоров И. А., Лютик А. И., Швец В. И., Кириллова Ю. Г.Рациональныйспособполученияпсевдопептидныхфрагментов–ключевыхинтермедиатов синтеза полиамидных миметиков нуклеиновых кислот (ПАНКМ). //Вестник МИТХТ. – 2013. – Т. 8 № 6. – C. 108-110.106.Chandrasekhar S., Reddy Ch.
R., Rao R. J. Facile and selective cleavage of allyl ethers,amines and esters using polymethylhydrosiloxane–ZnCl2/Pd(PPh3)4. // Tetrahedron. – 2001. – V.57. – P. 3435-3438.107.Friedrich-Bochnitschek S., Waldmann H., Kunz H. Allyl esters as carboxy protectinggroups in the synthesis of O-glycopeptides. // J. Org.
Chem. – 1989. – V. 54(4). – P. 751-756.108.Dueholm K. L., Petersen K. H., Jensen D. K., Egholm M., Nielsen P. E., Buchardt O.Peptide nucleic acid (PNA) with a chiral backbone based on alanine. // Bioorg. & Med. Chem.Letters. –1994. – V. 4(8). – P. 1077-1080.109.Sahu B., Sacui I., Rapireddy S., Zanotti K. J., Bahal R., Armitage B. A., Ly D. H.Synthesis and Characterization of Conformationally Preorganized, (R)-Diethylene GlycolContaining γ-Peptide Nucleic Acids with Superior Hybridization Properties and WaterSolubility. // J.
Org. Chem. – 2011. – V. 76. – P. 5614–5627.110.Huang H., Joe G. H., Choi S. R., Kim S. N., Kim Y. T., Pak C. S., Hong J. H., Lee W.Synthesis of Enantiopure γ-Glutamic Acid Functionalized Peptide Nucleic Acid Monomers. //Bull. Korean Chem. Soc. – 2010. – V. 31(7). – P. 2054-2056.111.Huang H., Joe G.
H., Choi S. R., Kim S. N., Kim Y. T., Pak H. S., Kim S. K., Hong J. H.,Han H.-K., Kang J. S., Lee W. Preparation and Determination of Optical Purity of γ-LysineModified Peptide Nucleic Acid Analogues. // Arch. Pharm. Res. – 2012. – V. 35(3). – P. 517522.112.Kuznetsov M.
