Although adducts resulting from the reaction of mitomycin C (MC) and DNA have been characterized as guanine derivatives covalently linked to MC at the guanine N2-and/or 06-positions, lack of material and of protons on the guanine nucleus had led to difficulties in product characterization. Authentic
Necessary protection of the O6-position of guanine during the solid phase synthesis of oligonucleotides by the phosphoramidite approach
β Scribed by Richard T. Pon; Masad J. Damha; Kelvin K. Ogilvie
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 227 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
It has been observed that the use of U6-protected deoxyguanosine phosphoramidites leads to a significant improvement in the automated synthesis of oligonucleotides on an insoluble support.
The introduction of deoxyribonucleoside-3'-phosphoKamidite derivatives by
Caruthers and Beaucagel has lead to the routine synthesis of short oligonucleo-
π SIMILAR VOLUMES
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Oligoribonucleotides, six to fifteen units long, were synthesized on a controlled pore glass support using ribonucleoside 3'-0-phosphoramidite reagents. Average coupling yieids of up to 98% were obtained with dirsopropylamrnophosphoramidite derivatives. In light of the increasing interest in the ro
The syntheses of N,N-diisopropylmethylphosphoramidites (3a,b) of 9-I [Zdimethoxytrityl-hydroxy-l-(hydroxymethyl)ethoxy]-methyl)N6-benzoyladenine, 2a, and l-{ [Zdimethoxytritylhydroxy-1-(hydroxymethyl)ethoxy]-methyl)thymine, 2b, are described. Oligoacyclonucleotides, 2 -8 units long, were synthesized