Efficient Pyrimidine N‐1‐Alkylation via Activation of Electron Rich Olefins with Oxoammonium Salts: Synthesis of Methoxy TEMPO Substituted Pyrimidine Nucleoside Analogs-Reference-Cited by-同舟云学术

Efficient Pyrimidine N‐1‐Alkylation via Activation of Electron Rich Olefins with Oxoammonium Salts: Synthesis of Methoxy TEMPO Substituted Pyrimidine Nucleoside Analogs

Published:2004-01-01 Issue:11 Volume:23 Page:1723-1738
ISSN:1525-7770
Container-title:Nucleosides, Nucleotides & Nucleic Acids
language:en
Short-container-title:Nucleosides, Nucleotides & Nucleic Acids

Author:

Church Kevin M.¹,Holloway Liesel M.¹,Matley Ryan C.¹,Brower Robert J.¹

Affiliation:

1. a Department of Chemistry , University of Dayton , 300 College Park, Dayton, Ohio, 45469, USA

Publisher

Informa UK Limited

Subject

Genetics,Molecular Medicine,Biochemistry,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1081/NCN-200034038

Reference29 articles.

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3. Synthesis of nucleosides. 9. General synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides

4. Nucleosides and nucleotides. LXII. Synthesis and optical properties of 2,3-dideoxy-D-erythro-hex-2-enopyranosyl nucleosides.

5. Furanoid Glycal as a Starting Material for Nucleoside Derivatives

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