169 related articles for article (PubMed ID: 2717397)
1. Solid-phase synthesis of oligoribonucleotides using 9-fluorenylmethoxycarbonyl (Fmoc) for 5'-hydroxyl protection.
Lehmann C; Xu YZ; Christodoulou C; Tan ZK; Gait MJ
Nucleic Acids Res; 1989 Apr; 17(7):2379-90. PubMed ID: 2717397
[TBL] [Abstract][Full Text] [Related]
2. Solid-phase synthesis of oligoribonucleotides.
Xu YZ; Lehmann C; Slim G; Christodoulou C; Tan ZK; Gait MJ
Nucleic Acids Symp Ser; 1989; (21):39-40. PubMed ID: 2608470
[TBL] [Abstract][Full Text] [Related]
3. The acetal levulinyl ester (ALE) group for the 2'-hydroxyl protection of ribonucleosides and the synthesis of oligoribonucleotides.
Lackey JG; Damha MJ
Nucleic Acids Symp Ser (Oxf); 2008; (52):35-6. PubMed ID: 18776240
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of oligoribonucleotides using the 2-nitrobenzyloxymethyl group for 2'-hydroxyl protection.
Miller TJ; Schwartz ME; Gough GR
Curr Protoc Nucleic Acid Chem; 2001 May; Chapter 3():Unit 3.7. PubMed ID: 18428847
[TBL] [Abstract][Full Text] [Related]
5. Synthesis of RNA oligomer using 9-fluorenylmethoxycarbonyl (Fmoc) group for 5'-hydroxyl protection.
Fukuda T; Hamana T; Marumoto R
Nucleic Acids Symp Ser; 1988; (19):13-6. PubMed ID: 2465536
[TBL] [Abstract][Full Text] [Related]
6. Chemical synthesis of RNA sequences with 2'-O-[(triisopropylsilyl)oxy]methyl-protected ribonucleoside phosphoramidites.
Pitsch S; Weiss PA
Curr Protoc Nucleic Acid Chem; 2002 Feb; Chapter 3():Unit 3.8. PubMed ID: 18428891
[TBL] [Abstract][Full Text] [Related]
7. Preparation of 2'-O-[(Triisopropylsilyl)oxy]methyl-protected ribonucleosides.
Pitsch S; Weiss PA
Curr Protoc Nucleic Acid Chem; 2002 Feb; Chapter 2():Unit 2.9. PubMed ID: 18428890
[TBL] [Abstract][Full Text] [Related]
8. Synthesis of 5'-Thio-3'-O-ribonucleoside Phosphoramidites.
Li NS; Lu J; Piccirilli JA
J Org Chem; 2017 Dec; 82(23):12003-12013. PubMed ID: 29049877
[TBL] [Abstract][Full Text] [Related]
9. A base-labile protecting group (fluorenylmethoxycarbonyl) for the 5'-hydroxy function of nucleosides.
Gait MJ; Lehmann C
Curr Protoc Nucleic Acid Chem; 2001 May; Chapter 2():Unit 2.4. PubMed ID: 18428837
[TBL] [Abstract][Full Text] [Related]
10. The 4-(N-dichloroacetyl-N-methylamino)benzyloxymethyl group for 2'-hydroxyl protection of ribonucleosides in the solid-phase synthesis of oligoribonucleotides.
Cieślak J; Grajkowski A; Kauffman JS; Duff RJ; Beaucage SL
J Org Chem; 2008 Apr; 73(7):2774-83. PubMed ID: 18327953
[TBL] [Abstract][Full Text] [Related]
11. Preparation of 5'-silyl-2'-orthoester ribonucleosides for use in oligoribonucleotide synthesis.
Scaringe SA; Kitchen D; Kaiser RJ; Marshall WS
Curr Protoc Nucleic Acid Chem; 2004 May; Chapter 2():Unit 2.10. PubMed ID: 18428924
[TBL] [Abstract][Full Text] [Related]
12. Synthesis of isotopically labeled D-[1'-13C]ribonucleoside phosphoramidites.
Saito Y; Nyilas A; Agrofoglio LA
Carbohydr Res; 2001 Mar; 331(1):83-90. PubMed ID: 11284508
[TBL] [Abstract][Full Text] [Related]
13. Acetal levulinyl ester (ALE) groups for 2'-hydroxyl protection of ribonucleosides in the synthesis of oligoribonucleotides on glass and microarrays.
Lackey JG; Mitra D; Somoza MM; Cerrina F; Damha MJ
J Am Chem Soc; 2009 Jun; 131(24):8496-502. PubMed ID: 19485360
[TBL] [Abstract][Full Text] [Related]
14. Chemical synthesis of oligoribonucleotides with 2'-O-(2-cyanoethoxymethyl)-protected phosphoramidites.
Ohgi T; Kitagawa H; Yano J
Curr Protoc Nucleic Acid Chem; 2008 Sep; Chapter 2():Unit 2.15. PubMed ID: 18819083
[TBL] [Abstract][Full Text] [Related]
15. Fmoc/solid-phase synthesis of Tyr(P)-containing peptides through t-butyl phosphate protection.
Perich JW; Reynolds EC
Int J Pept Protein Res; 1991 Jun; 37(6):572-5. PubMed ID: 1717394
[TBL] [Abstract][Full Text] [Related]
16. 5'-Levulinyl and 2'-tetrahydrofuranyl protection for the synthesis of oligoribonucleotides by the phosphoramidite approach.
Iwai S; Ohtsuka E
Nucleic Acids Res; 1988 Oct; 16(20):9443-56. PubMed ID: 3186438
[TBL] [Abstract][Full Text] [Related]
17. Solid phase synthesis of mRNA by the phosphoramidite approach using 2'-O-1-(2-chloroethoxy)ethyl protection and its stability in E. coli system.
Sakatsume O; Yamaguchi T; Takaku H
Nucleic Acids Symp Ser; 1991; (24):33-6. PubMed ID: 1841372
[TBL] [Abstract][Full Text] [Related]
18. Synthesis and applications of oligoribonucleotides with selected 2'-O-methylation using the 2'-O-[1-(2-fluorophenyl)-4-methoxypiperidin-4-yl] protecting group.
Beijer B; Sulston I; Sproat BS; Rider P; Lamond AI; Neuner P
Nucleic Acids Res; 1990 Sep; 18(17):5143-51. PubMed ID: 2402441
[TBL] [Abstract][Full Text] [Related]
19. Selective 2'-benzoylation at the cis 2',3'-diols of protected ribonucleosides. New solid phase synthesis of RNA and DNA-RNA mixtures.
Kempe T; Chow F; Sundquist WI; Nardi TJ; Paulson B; Peterson SM
Nucleic Acids Res; 1982 Nov; 10(21):6695-714. PubMed ID: 6184676
[TBL] [Abstract][Full Text] [Related]
20. A whole base-labile strategy for RNA synthesis with 2'-O-acetalester protections.
Lavergne T; Martin A; Debart F; Vasseur JJ
Nucleic Acids Symp Ser (Oxf); 2008; (52):51-2. PubMed ID: 18776248
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
