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A new strategy for the protection of deoxyguanosine during oligonucleotide synthesis

✍ Scribed by B.L. Gaffney; R.A. Jones


Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
237 KB
Volume
23
Category
Article
ISSN
0040-4039

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✦ Synopsis


The protection of the 6-0~0 group of deoxyguanosine with the Z-trimsthylsilylethyl (L), phenylthioethyl (A), 4-nitrophenylthioethyl (5). 4-nitrophenethyl (J), and cyanoethyl (6) groups is described. is cleaved udder mild conditions.

Each protectin

group is introduced in good yield and Compatibility with the various approaches to oligonucleotide synthesis is discussed.


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