Enantioselective Synthesis of Homo-N-Nucleosides Containing a 1,4-Dioxane Sugar Analog
Author:
Publisher
MDPI AG
Subject
Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science
Link
http://www.mdpi.com/1420-3049/13/12/2962/pdf
Reference25 articles.
1. Sugar-Modified Nucleosides in Past 10 Years, A Review
2. New developments in the enantioselective synthesis of cyclopentyl carbocyclic nucleosides;Crimmins;Tetrahedron,1998
3. AIDS-driven nucleoside chemistry.
4. Synthesis of homo-N-nucleosides, a series of C1' branched-chain nucleosides
5. Homo-N-nucleosides: Incorporation into oligonucleotides and antiviral activity
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1. Synthesis of Functionalized 1,4-Dioxanes with an Additional (Hetero)Aliphatic Ring;Synthesis;2018-07-20
2. Nucleosides 9: Design and synthesis of new 8-nitro and 8-amino xanthine nucleosides of expected biological activity;Nucleosides, Nucleotides and Nucleic Acids;2017-12-02
3. Effective Synthesis of Nucleosides Utilizing O-Acetyl-Glycosyl Chlorides as Glycosyl Donors in the Absence of Catalyst: Mechanism Revision and Application to Silyl-Hilbert-Johnson Reaction;Molecules;2017-01-05
4. Synthesis of Novel Homo-N-Nucleoside Analogs Composed of a Homo-1,4-Dioxane Sugar Analog and Substituted 1,3,5-Triazine Base Equivalents;Molecules;2008-12-10
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