Synthesis of Truncated Carbocyclic Nucleosides Using 5′‐Deoxy‐5′‐Heteroarylsulfonylnucleosides-Reference-Cited by-同舟云学术

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Synthesis of Truncated Carbocyclic Nucleosides Using 5′‐Deoxy‐5′‐Heteroarylsulfonylnucleosides

Published:2022-03 Issue:3 Volume:2 Page:
ISSN:2691-1299
Container-title:Current Protocols
language:en
Short-container-title:Current Protocols

Author:

Oka Natsuhisa¹²³^ORCID,Kanda Mayuka¹,Furuzawa Minami¹,Arai Wakaba¹,Ando Kaori¹

Affiliation:

1. Department of Chemistry and Biomolecular Science, Faculty of Engineering Gifu University Gifu Japan

2. Center for Highly Advanced Integration of Nano and Life Sciences (G‐CHAIN) Gifu University Gifu Japan

3. Institute for Glyco‐core Research (iGCORE) Gifu University Gifu Japan

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cpz1.398

Reference28 articles.

1. 1-Methyl-1H-tetrazol-5-yl (MT) sulfones in the Julia-Kocienski olefination: Comparison with the PT and the TBT sulfones

2. Stereoselective Synthesis of Trisubstituted (Z)-Alkenes from Ketones via the Julia–Kocienski Olefination Using 1-Methyl- and 1-tert-Butyl-1H-tetrazol-5-yl Alkyl Sulfones

3. The Julia-Kocienski Olefination

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