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
Hauptverfasser: Ogilvie, Kelvin K, Nemer, Mona J
Format: Artikel
Sprache:eng
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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.
ISSN:0008-4042
1480-3291
DOI:10.1139/v80-219