Nucleic acid analog with amide linkage and method of making that

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

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536 231, 536 253, 536 2531, 536 2532, 435 6, 935 76, 935 77, 935 78, C07H 1900, C12Q 168, C12N 1500

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056376839

ABSTRACT:
The present invention relates to a nucleic acid analog having the formula: ##STR1## where R is a compound selected from a group consisting of hydrogen, a hydroxyl group, a hydrophilic group or a hydrophobic group,

REFERENCES:
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Chur, et al., "Synthesis of a Carboxamide Linked T*T Dimer and its Incorporation in Oligonucleotides," Nucleic Acids Research, 21(22):5179-83 (1993).
Lebreton, et al., "Synthesis of Thymidine Dimer Derivatives Containing an Amide Linkage and Their Incorporation Into Oligodeoxyribonucleotides," Tetrahedron Letters, 34(40):6383-86 (1993).
De Mesmaeker, et al., "Novel Backbone Replacements for Oligonucleotides," in Carbohydrate Modifications in Antisense Research, 24-39, Yogesh Sanghui and P. Dan Cook, Eds. (1994).
De Mesmaeker, et al., "Amides as a New Type of Backbone Modification in Oligonucleotides," Angew. Chem. Int. Ed. Engl., 33(2):226-29 (1994).
Verheggen et al. "Synthesis and Antiherpes Virus Activity of 1,5-Anhydrohexitol Nucleosides" J. Med. Chem., vol. 36, pp. 2033-2040 1993.
Jois et al. "Synthesis and Antiviral Evaluation of Some Novel [1,2,4]Triazolo[4,3-b][1,2,4]triazole Nucleoside Analogs" J. Heterocyclic Chem., vol. 30, pp. 1289-1292 1993.
Neidlein et al. "Syntheses and Investigations of [Oxazolo[2,3-a]isoindol-9b(2H)-yl]phosphonates and phosphinates: a New Class of Heterocycles" Helv. Chim. Acta, vol. 76, pp. 2407-2417 1993.

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