Synthesis and Reactivity of Spirocarbocycles as Scaffolds for Nucleoside Analogues-Reference-Cited by-同舟云学术

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Synthesis and Reactivity of Spirocarbocycles as Scaffolds for Nucleoside Analogues

Published:2020-11-16 Issue:23 Volume:85 Page:14989-15005
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Verhoeven Jonas¹²^ORCID,Deraet Xavier³^ORCID,Pande Vineet²,Sun Weimei²,Alonso Mercedes³^ORCID,De Proft Frank³,Meerpoel Lieven²,Thuring Jan Willem²^ORCID,Verniest Guido¹²

Affiliation:

1. Research Group of Organic Chemistry (ORGC), Department of Chemistry and Department of Bio-Engineering Sciences, Faculty of Science and Bio-Engineering Sciences, Vrije Universiteit Brussel (VUB) Pleinlaan 2, 1050 Brussels, Belgium

2. Janssen Pharmaceutica NV Turnhoutseweg 30, 2340 Beerse, Belgium

3. Research Group of General Chemistry (ALGC), Vrije Universiteit Brussel (VUB), 1050 Brussels, Belgium

Funder

Vrije Universiteit Brussel

Fonds Wetenschappelijk Onderzoek

Agentschap voor Innovatie door Wetenschap en Technologie

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c01825

Reference58 articles.

1. Carbocyclic nucleosides

2. bAgrofoglio, L. A.; Challand, S. R. Acyclic, Carbocyclic and L-Nucleosides—the Chemistry of Carbocyclic Nucleosides; Kluwer Academic Publishers: Dordrecht, 1998; pp 174–284.

3. Advances in the enantioselective synthesis of carbocyclic nucleosides

4. bLeclerc, E. Chemical Synthesis of Nucleoside Analogues; Wiley, 2013; pp 535–604.

5. cMieczkowski, A.; Agrofoglio, L. A. Synthesis and Biological Activity of Selected Carbocyclic Nucleosides; Wiley-VCH, 2008; pp 393–424.

Cited by 2 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. Ketoreductase-Mediated Stereodivergent Synthesis of 1,1-Disubstituted Cyclobutan-3-ols;Organic Process Research & Development;2024-05-21

2. Chemical Approaches to Carbocyclic Nucleosides;The Chemical Record;2022-02-04

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