Chemo-, regio- and stereoselective Mitsunobu reaction of unprotected pyrimidine bases with hydroxypyrrolidines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Formal Desymmetrization by a “Mitsunobu Trick” − Enantiomerically Purecis-3,4-DihydroxypyrrolineN-Oxides for the Enantiodivergent Synthesis of Trihydroxyindolizidines
2. Synthesis of Enantiopure 3-Substituted Pyrroline N-Oxides by Highly Regioselective Oxidation of the Parent Hydroxylamines: A Mechanistic Rationale
3. Nucleoside Analogues as Chemotherapeutic Agents: A Review
4. Modulation of leukocyte genetic expression by novel purine nucleoside analogs. A new approach to antitumor and antiviral agents
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3. An Efficient Route to Acyclic C-Nucleosides and Fused-Ring Analogues of Uridine from exo-Glycals;The Journal of Organic Chemistry;2009-09-30
4. Mitsunobu and Related Reactions: Advances and Applications;Chemical Reviews;2009-04-21
5. C2-Symmetric Pyrrolidines Derived from Tartaric Acids: Versatile Chiral Building Blocks for Total Synthesis, Catalyst Design, Supramolecular and Medicinal Chemistry;Current Organic Synthesis;2009-02-01
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