Phosphoramidit-Synthese (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Phosphoramidit-Synthese" in German language version.

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  • Beaucage, S.L.; Marvin H. Caruthers: Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis. In: Tetrahedron Letters. 22. Jahrgang, 1981, S. 1859–1862, doi:10.1016/S0040-4039(01)90461-7.
  • Lin, K.-Y., Matteucci, M. D.: A cytosine analog capable of clamp-like binding to a guanine in helical nucleic acids. In: J. Am. Chem. Soc. 120. Jahrgang, Nr. 33, 1998, S. 8531–8532, doi:10.1021/ja981286z.
  • Nielsen, J.; Taagaard, M.; Marugg, J. E.; Van Boom, J. H.; Dahl, O.: Application of 2-cyanoethyl N,N,N′,N′-tetraisopropylphosphorodiamidite for in situ preparation of deoxyribonucleoside phosphoramidites and their use in polymer-supported synthesis of oligodeoxyribonucleotides. In: Nucl. Acids Res. 14. Jahrgang, Nr. 18, 1986, S. 7391–7403, doi:10.1093/nar/14.18.7391.
  • Nielsen, J.; Dahl, O.: Improved synthesis of 2-cyanoethyl N,N,N′,N′-tetraisopropylphosphorodiamidite (iPr2N)2POCH2CH2CN. In: Nucl. Acids Res. 15. Jahrgang, Nr. 8, 1987, S. 3626, doi:10.1093/nar/15.8.3626.
  • Beaucage, S. L.: 2-Cyanoethyl Tetraisopropylphosphorodiamidite. In: e-EROS Encyclopedia of Reagents for Organic Synthesis. 2001, doi:10.1002/047084289X.rn00312.
  • Sinha, N. D.; Biernat, J.; Koester, H.: β-Cyanoethyl N,N-dialkylamino/N-morpholinomonochloro phosphoamidites, new phosphitylating agents facilitating ease of deprotection and work-up of synthesized oligonucleotides. In: Tetrahedron Lett. 24. Jahrgang, Nr. 52, 1983, S. 5843–5846, doi:10.1016/S0040-4039(00)94216-3.
  • Marugg, J. E.; Burik, A.; Tromp, M.; Van der Marel, G. A.; Van Boom, J. H.: A new and versatile approach to the preparation of valuable deoxynucleoside 3′-phosphite intermediates. In: Tetrahedron Lett. 24. Jahrgang, Nr. 20, 1986, S. 2271–22274, doi:10.1016/S0040-4039(00)84506-2.
  • Guzaev, A. P.; Manoharan, M.: 2-Benzamidoethyl group - a novel type of phosphate protecting group for oligonucleotide synthesis. In: J. Amer. Chem. Soc. 123. Jahrgang, Nr. 5, 2001, S. 783–793, doi:10.1021/ja0016396.
  • Sproat, B.; Colonna, F.; Mullah, B.; Tsou, D.; Andrus, A.; Hampel, A.; Vinayak, R.: An efficient method for the isolation and purification of oligoribonucleotides. In: Nucleosides & Nucleotides. 14. Jahrgang, Nr. 1&2, Februar 1995, ISSN 0261-3166, S. 255–273, doi:10.1080/15257779508014668.
  • Stutz, A.; Hobartner, C.; Pitsch, S.: Novel fluoride-labile nucleobase-protecting groups for the synthesis of 3'(2')-O-amino-acylated RNA sequences. In: Helv. Chim. Acta. 83. Jahrgang, Nr. 9, September 2000, ISSN 0018-019X, S. 2477–2503, doi:10.1002/1522-2675(20000906)83:9<2477::AID-HLCA2477>3.0.CO;2-9.
  • Welz, R.; Muller, S.: 5-(Benzylmercapto)-1H-tetrazole as activator for 2′-O-TBDMS phosphoramidite building blocks in RNA synthesis. In: Tetrahedron Letters. 43. Jahrgang, Nr. 5, Januar 2002, ISSN 0040-4039, S. 795–797, doi:10.1016/S0040-4039(01)02274-2.
  • Vargeese, C.; Carter, J.; Yegge, J.; Krivjansky, S.; Settle, A.; Kropp, E.; Peterson, K.; Pieken, W.: Efficient activation of nucleoside phosphoramidites with 4,5-dicyanoimidazole during oligonucleotide synthesis. In: Nucl. Acids Res. 26. Jahrgang, Nr. 4, 1998, ISSN 0305-1048, S. 1046–1050, doi:10.1093/nar/26.4.1046, PMID 9461466, PMC 147346 (freier Volltext).
  • Guzaev, A. P.: Reactivity of 3H-1,2,4-dithiazole-3-thiones and 3H-1,2-dithiole-3-thiones as sulfurizing agents for oligonucleotide synthesis. In: Tetrahedron Letters. 52. Jahrgang, 2011, S. 434–437, doi:10.1016/j.tetlet.2010.11.086.
  • Ravikumar, V. T.; Kumar, R. K.: Stereoselective Synthesis of Alkylphosphonates: A Facile Rearrangement of Cyanoethyl-Protected Nucleoside Phosphoramidites. In: Org. Process Res. Dev. 8. Jahrgang, Nr. 4, 2004, S. 603–608, doi:10.1021/op030035u.
  • Gryaznov, S. M.; Letsinger, R. L.: Synthesis of oligonucleotides via monomers with unprotected bases. In: J. Amer. Chem. Soc. 113. Jahrgang, Nr. 15, 1991, S. 5876–5877, doi:10.1021/ja00015a059.
  • Reddy, M. P.; Hanna, N. B.; Farooqui, F.: Ultrafast Cleavage and Deprotection of Oligonucleotides Synthesis and Use of CAc Derivatives. In: Nucleosides & Nucleotides. 16. Jahrgang, 1997, S. 1589–1598, doi:10.1080/07328319708006236.
  • McMinn, D.: Synthesis of oligonucleotides containing 3′-alkyl amines using N-isobutyryl protected deoxyadenosine phosphoramidite. In: Tetrahedron Lett. 38. Jahrgang, 1997, S. 3123, doi:10.1016/S0040-4039(97)00568-6.
  • Schulhof, J. C.; Molko, D.; Teoule, R.: The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups. In: Nucleic Acids Res. 15. Jahrgang, Nr. 2, 1987, S. 397–416, doi:10.1093/nar/15.2.397, PMID 3822812, PMC 340442 (freier Volltext).
  • Zhu, Q.: Observation and elimination of N-acetylation of oligonucleotides prepared using fast-deprotecting phosphoramidites and ultra-mild deprotection. In: Bioorg. & Med. Chem. Lett. 11. Jahrgang, 2001, S. 1105, doi:10.1016/S0960-894X(01)00161-5.
  • McBride, L. J., R. Kierzek, S. L. Beaucage, M. H. Caruthers: Nucleotide chemistry. 16. Amidine protecting groups for oligonucleotide synthesis. In: J. Amer. Chem. Soc. 108. Jahrgang, 1986, S. 2040, doi:10.1021/ja00268a052.
  • Sinha, N. D.; Biernat, J.; McManus, J.; Koester, H.: Polymer support oligonucleotide synthesis. XVIII: use of β-cyanoethyl-N,N-dialkylamino-/N-morpholino phosphoramidite of deoxynucleosides for the synthesis of DNA fragments simplifying deprotection and isolation of the final product. In: Nucleic Acids Res. 12. Jahrgang, Nr. 11, 1984, S. 4539–4557, doi:10.1093/nar/12.11.4539, PMID 6547529, PMC 318857 (freier Volltext).
  • Guzaev, A. P.; Manoharan, M.: Phosphoramidite Coupling to Oligonucleotides Bearing Unprotected Internucleosidic Phosphate Moieties. In: J. Org. Chem. 66. Jahrgang, Nr. 5, 2001, S. 1798–1804, doi:10.1021/jo001591e, PMID 11262130.
  • Ogilvie, K. K.; Theriault, N.; Sadana, K. L.: Synthesis of oligoribonucleotides. In: J. Amer. Chem. Soc. 99. Jahrgang, Nr. 23, 1977, S. 7741–7743, doi:10.1021/ja00465a073.
  • Usman, N.; Ogilvie, K. K.; Jiang, M. Y.; Cedergren, R. J.: The automated chemical synthesis of long oligoribuncleotides using 2′-O-silylated ribonucleoside 3′-O-phosphoramidites on a controlled-pore glass support: synthesis of a 43-nucleotide sequence similar to the 3′-half molecule of an Escherichia coli formylmethionine tRNA. In: J. Amer. Chem. Soc. 109. Jahrgang, Nr. 25, 1987, S. 7845–7854, doi:10.1021/ja00259a037.
  • Usman, N.; Pon, R. T.; Ogilvie, K. K.: Preparation of ribonucleoside 3′-O-phosphoramidites and their application to the automated solid phase synthesis of oligonucleotides. In: Tetrahedron Lett. 26. Jahrgang, Nr. 38, 1985, S. 4567–4570, doi:10.1016/S0040-4039(00)98753-7.
  • Scaringe, S. A.; Francklyn, C.; Usman, N.: Chemical synthesis of biologically active oligoribonucleotides using β-cyanoethyl protected ribonucleoside phosphoramidites. In: Nucl. Acids Res. 18. Jahrgang, Nr. 18, 1990, S. 5433–5441, doi:10.1093/nar/18.18.5433.
  • Pitsch, S.; Weiss, P. A.; Wu, X.; Ackermann, D.; Honegger, T.: Fast and reliable automated synthesis of RNA and partially 2′-O-protected precursors ("caged RNA") based on two novel, orthogonal 2′-O-protecting groups. In: Helv. Chim. Acta. 82. Jahrgang, Nr. 10, 1999, S. 1753–1761, doi:10.1002/(SICI)1522-2675(19991006)82:10<1753::AID-HLCA1753>3.0.CO;2-Y.
  • Pitsch, S.; Weiss, P. A.; Jenny, L.; Stutz, A.; Wu, X.: Reliable chemical synthesis of oligoribonucleotides (RNA) with 2′-O-[(triisopropylsilyl)oxy]methyl(2′-O-tom)-protected phosphoramidites. In: Helv. Chim. Acta. 84. Jahrgang, Nr. 12, 2001, S. 3773–3795, doi:10.1002/1522-2675(20011219)84:12<3773::AID-HLCA3773>3.0.CO;2-E.
  • S. Fang, S. Fueangfung, Y. Yuan: Purification of synthetic oligonucleotides via catching by polymerization. In: Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.]. Chapter 10Juni 2012, S. Unit10.14, ISSN 1934-9289. doi:10.1002/0471142700.nc1014s49. PMID 22700335.

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  • Vargeese, C.; Carter, J.; Yegge, J.; Krivjansky, S.; Settle, A.; Kropp, E.; Peterson, K.; Pieken, W.: Efficient activation of nucleoside phosphoramidites with 4,5-dicyanoimidazole during oligonucleotide synthesis. In: Nucl. Acids Res. 26. Jahrgang, Nr. 4, 1998, ISSN 0305-1048, S. 1046–1050, doi:10.1093/nar/26.4.1046, PMID 9461466, PMC 147346 (freier Volltext).
  • Schulhof, J. C.; Molko, D.; Teoule, R.: The final deprotection step in oligonucleotide synthesis is reduced to a mild and rapid ammonia treatment by using labile base-protecting groups. In: Nucleic Acids Res. 15. Jahrgang, Nr. 2, 1987, S. 397–416, doi:10.1093/nar/15.2.397, PMID 3822812, PMC 340442 (freier Volltext).
  • Sinha, N. D.; Biernat, J.; McManus, J.; Koester, H.: Polymer support oligonucleotide synthesis. XVIII: use of β-cyanoethyl-N,N-dialkylamino-/N-morpholino phosphoramidite of deoxynucleosides for the synthesis of DNA fragments simplifying deprotection and isolation of the final product. In: Nucleic Acids Res. 12. Jahrgang, Nr. 11, 1984, S. 4539–4557, doi:10.1093/nar/12.11.4539, PMID 6547529, PMC 318857 (freier Volltext).
  • Guzaev, A. P.; Manoharan, M.: Phosphoramidite Coupling to Oligonucleotides Bearing Unprotected Internucleosidic Phosphate Moieties. In: J. Org. Chem. 66. Jahrgang, Nr. 5, 2001, S. 1798–1804, doi:10.1021/jo001591e, PMID 11262130.
  • S. Fang, S. Fueangfung, Y. Yuan: Purification of synthetic oligonucleotides via catching by polymerization. In: Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.]. Chapter 10Juni 2012, S. Unit10.14, ISSN 1934-9289. doi:10.1002/0471142700.nc1014s49. PMID 22700335.

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  • Sproat, B.; Colonna, F.; Mullah, B.; Tsou, D.; Andrus, A.; Hampel, A.; Vinayak, R.: An efficient method for the isolation and purification of oligoribonucleotides. In: Nucleosides & Nucleotides. 14. Jahrgang, Nr. 1&2, Februar 1995, ISSN 0261-3166, S. 255–273, doi:10.1080/15257779508014668.
  • Stutz, A.; Hobartner, C.; Pitsch, S.: Novel fluoride-labile nucleobase-protecting groups for the synthesis of 3'(2')-O-amino-acylated RNA sequences. In: Helv. Chim. Acta. 83. Jahrgang, Nr. 9, September 2000, ISSN 0018-019X, S. 2477–2503, doi:10.1002/1522-2675(20000906)83:9<2477::AID-HLCA2477>3.0.CO;2-9.
  • Welz, R.; Muller, S.: 5-(Benzylmercapto)-1H-tetrazole as activator for 2′-O-TBDMS phosphoramidite building blocks in RNA synthesis. In: Tetrahedron Letters. 43. Jahrgang, Nr. 5, Januar 2002, ISSN 0040-4039, S. 795–797, doi:10.1016/S0040-4039(01)02274-2.
  • Vargeese, C.; Carter, J.; Yegge, J.; Krivjansky, S.; Settle, A.; Kropp, E.; Peterson, K.; Pieken, W.: Efficient activation of nucleoside phosphoramidites with 4,5-dicyanoimidazole during oligonucleotide synthesis. In: Nucl. Acids Res. 26. Jahrgang, Nr. 4, 1998, ISSN 0305-1048, S. 1046–1050, doi:10.1093/nar/26.4.1046, PMID 9461466, PMC 147346 (freier Volltext).
  • S. Fang, S. Fueangfung, Y. Yuan: Purification of synthetic oligonucleotides via catching by polymerization. In: Current protocols in nucleic acid chemistry / edited by Serge L. Beaucage ... [et al.]. Chapter 10Juni 2012, S. Unit10.14, ISSN 1934-9289. doi:10.1002/0471142700.nc1014s49. PMID 22700335.