Synthesis of novel polycylic nucleoside analogues, incorporation into oligodeoxynucleotides, and interaction with complementary sequences

DOI: 10.1021/ja00190a044

Source and publish data:

Journal of the American Chemical Society p. 3041 - 3046 (1989)

Update date:2022-09-26

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Authors:

Bischofberger

Matteucci

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Article abstract of DOI:10.1021/ja00190a044

4-O-[(Triisopropylphenyl)sulfonyl]pyrimidine nucleosides were reacted with aromatic diamines leading to fused, polycylic ring systems: o-phenylenediamine yielded the pyrimido[1,6-a]benzimidazole, 2,3-diaminonaphthalene gave the naphth[2',3':4,5]imidazo[1,

Full text of DOI:10.1021/ja00190a044

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Article Doi

Synthesis of novel polycylic nucleoside analogues, incorporation into oligodeoxynucleotides, and interaction with complementary sequences

DOI: 10.1021/ja00190a044

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00190a044

Full text of DOI:10.1021/ja00190a044

Products guided by the article

R&D Labs maybe for 119693-96-8

Relevant to this article

Rh(II)-catalysed reactions of 2H-azirines with ethyl 2-acyl-2- diazoacetates. Synthesis of novel photochromic oxazines

Small molecule inhibitors of Myc/Max dimerization and Myc-induced cell transformation

Silver oxide as a novel catalyst for carbon-carbon bond-forming reactions in aqueous media

Iron-catalyzed ligand-free carbon-selenium (or tellurium) coupling of arylboronie acids with diselenides and ditellurides

Studies toward the synthesis of inhibitors of mycobacterium tuberculosis cell-wall biosynthesis: The assembly of triazole-linked 1,6-a-D-oligomannosides via click CuAAC

Coordination chemistry approach to the long-standing challenge of stereocontrolled chemical glycosylation