The synthesis of oligoribonucleotides VI. The synthesis of a hexadecamer by a block condensation approach
The synthesis of the 5′-monomethoxytrityl-2′-tert-butyldimethylsilyl-3′-levulinylribonucleosides 4 of the four major bases involved in the phosphite procedure for the synthesis of oligoribonucleotides is described along with the 2′,3′-isomeric derivatives 6 . This report describes a total protection...
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Veröffentlicht in: | Canadian journal of chemistry 1980-07, Vol.58 (14), p.1389-1397 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The synthesis of the 5′-monomethoxytrityl-2′-tert-butyldimethylsilyl-3′-levulinylribonucleosides
4
of the four major bases involved in the phosphite procedure for the synthesis of oligoribonucleotides is described along with the 2′,3′-isomeric derivatives
6
. This report describes a total protection system for nucleotide units which allows for the block condensation procedure to be used for the synthesis of long chains. The procedure is illustrated by the synthesis of a hexadecauridylic acid. |
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ISSN: | 0008-4042 1480-3291 |
DOI: | 10.1139/v80-219 |