Wolfrom et al., 1965 - Google Patents
The Anomeric 9-(2-Amino-2-deoxy-D-glucopyranosyl) adenines1, 2Wolfrom et al., 1965
- Document ID
- 15905246582971876760
- Author
- Wolfrom M
- Garg H
- Horton D
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
Condensation of 3, 4, 6-tri-0-acetyl-2-deoxy-2-(2, 4-dinitroanilino)-an-glucopyranosyl bromide (I) with 6-acetamido-9-chloromercuripurine gives thecrystalline blocked nucleoside derivative 6-acetamido-9-[3, 4, 6-tri-0-acetyl-2-deoxy-2-(2, 4-dinitroanilino)-/3-o …
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 NC1=NC=NC2=C1N=CN2 0 abstract description 22
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- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
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- C07H13/12—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by acids having the group -X-C(=X)-X-, or halides thereof, in which each X means nitrogen, oxygen, sulfur, selenium or tellurium, e.g. carbonic acid, carbamic acid
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H3/00—Compounds containing only hydrogen atoms and saccharide radicals having only carbon, hydrogen, and oxygen atoms
- C07H3/02—Monosaccharides
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- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H9/00—Compounds containing a hetero ring sharing at least two hetero atoms with a saccharide radical
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- C07—ORGANIC CHEMISTRY
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- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
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- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
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- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
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