Advantages of the Ns group in the reactions of N1-SO2R inosines with benzylamine and with 15NH3-Reference-Cited by-同舟云学术

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Advantages of the Ns group in the reactions of N1-SO2R inosines with benzylamine and with 15NH3

Published:2005-08 Issue:31 Volume:46 Page:5127-5130
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Terrazas Montserrat,Ariza Xavier,Vilarrasa Jaume

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Bou, V. Ph.D. Thesis; Universitat de Barcelona, 1992

2. A Short Route to[3-15N]-3′-Azido-3′-deoxythymidine(N3-Labeled AZT) via 3-Nitro-AZT

3. Ariza, X. Ph.D. Thesis; Universitat de Barcelona, 1995.

4. A New Route to 15N-Labeled, N-Alkyl, and N-Amino Nucleosides via N-Nitration of Uridines and Inosines

5. N-Nitration, 15N-Labeling, and N-to-N Linking of Hydroxyl-Silylated Pyrimidine Nucleosides

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Applications of Purine Ring Opening in the Synthesis of Imidazole, Pyrimidine, and New Purine Derivatives;European Journal of Organic Chemistry;2021-08-26

2. Pd-catalysed amidation of 2,6-dihalopurine nucleosides. Replacement of iodine at 0°C;Tetrahedron Letters;2012-03

3. 15N Double-Labeled Guanosine from Inosine through Ring-Opening−Ring-Closing and One-Pot Pd-Catalyzed C−O and C−N Cross-Coupling Reactions;The Journal of Organic Chemistry;2010-06-15

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