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Volumn 24, Issue 5-7, 2005, Pages 1111-1114

4,5-Bis(ethoxycarbonyl)-[1,3]dioxolan-2-yl as a new orthoester-type protecting group for the 2′-hydroxyl function in the chemical synthesis of RNA

Author keywords

2 Ethoxy 1,3 Dioxolane 4,5 Dicarboxylic Acid Diethyl Ester; Acid Stability; RNA Protecting Group

Indexed keywords

1,3 DIOXOLANE DERIVATIVE; 4,5 BIS(ETHOXYCARBONYL)[1,3]DIOXOLAN 2 YL DERIVATIVE; ACID; ESTER; HYDROXYL GROUP; OLIGONUCLEOTIDE; ORGANIC SOLVENT; RNA; UNCLASSIFIED DRUG;

EID: 26644449853     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1081/NCN-200061895     Document Type: Conference Paper
Times cited : (6)

References (6)
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    • Reese, C.B. The chemical synthesis of oligo- and poly-nucleotides: a personal commentary. Tetrahedron 2002, 58, 8893.
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  • 2
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    • Cyclic orthoester functions as new protecting groups in nucleosides
    • Sekine, M.; Hata, T. Cyclic orthoester functions as new protecting groups in nucleosides. J. Am. Chem. Soc. 1983, 105, 2044-20049.
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  • 3
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    • The synthesis of oligoribonucleotides-VIII: The preparation of ribonucleoside 2′,5′-bisketals
    • Green, L.P.D.; Ravindranathan, R.; Reese, C.B.; Saffihill, R. The synthesis of oligoribonucleotides-VIII: the preparation of ribonucleoside 2′,5′-bisketals. Tetrahedron 1970, 26, 1031-1041.
    • (1970) Tetrahedron , vol.26 , pp. 1031-1041
    • Green, L.P.D.1    Ravindranathan, R.2    Reese, C.B.3    Saffihill, R.4
  • 4
    • 0021983261 scopus 로고
    • Chemical synthesis of a pentaribonucleoside tetraphosphate constituting the 3′-acceptor stem sequence of E. coli tRNAIIe using 2′-O-(3-methoxy-1,5-dicarbomethoxypentan-3-yl)-ribonucleoside building blocks. Application of a new achiral and acid-labile 2′-hydroxyl protecting group in tRNA synthesis
    • Sandstrom, S.; Kwiatkowski, A.; Chattopadyaya, J. Chemical synthesis of a pentaribonucleoside tetraphosphate constituting the 3′-acceptor stem sequence of E. coli tRNAIIe using 2′-O-(3-methoxy-1,5- dicarbomethoxypentan-3-yl)-ribonucleoside building blocks. Application of a new achiral and acid-labile 2′-hydroxyl protecting group in tRNA synthesis. J. Acta Chem. Scand., B 1985, 39, 273-280.
    • (1985) J. Acta Chem. Scand., B , vol.39 , pp. 273-280
    • Sandstrom, S.1    Kwiatkowski, A.2    Chattopadyaya, J.3
  • 5
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    • RNA oligonucleotide synthesis via 5′-silyl-2′-orthoester chemistry
    • Scaringe, S.A. RNA oligonucleotide synthesis via 5′-silyl-2′- orthoester chemistry. Methods 2001, 23, 206-217.
    • (2001) Methods , vol.23 , pp. 206-217
    • Scaringe, S.A.1
  • 6
    • 0029999165 scopus 로고    scopus 로고
    • Synthesis of [4,5-bis(hydroxymethyl)-1,3-dioxolan-2-yl]nucleosides as potential inhibitors of HIV
    • Branalt, J.; Kvarnstrom, I.; Classon, B.; Samuelsson, B. Synthesis of [4,5-bis(hydroxymethyl)-1,3-dioxolan-2-yl]nucleosides as potential inhibitors of HIV. J. Org. Chem. 1996, 61, 3599-3603.
    • (1996) J. Org. Chem. , vol.61 , pp. 3599-3603
    • Branalt, J.1    Kvarnstrom, I.2    Classon, B.3    Samuelsson, B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.