Sign In

Login

Password

Forgot Password ? Sign Up

Phosphoramidit-Synthese (German Wikipedia)

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

refsWebsite
Global rank German rank
29doi.org
2nd place
3rd place
5zdb-katalog.de
123rd place
6th place
5nih.gov
4th place
7th place
1appliedbiosystems.com
low place
low place
1biosearchtech.com
low place
low place
1chemgenes.com
low place
low place
1glenresearch.com
low place
low place
1thermofisher.com
low place
low place
1atdbio.com
low place
low place

appliedbiosystems.com

products.appliedbiosystems.com

atdbio.com

biosearchtech.com

chemgenes.com

doi.org

  • 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.

glenresearch.com

nih.gov

ncbi.nlm.nih.gov

  • 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.

thermofisher.com

zdb-katalog.de

  • 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.