Synthesis of 4′/5′-Spirocyclopropanated Uridine and d-Xylouridine Derivatives and Their Activity against the Human Respiratory Syncytial Virus-Reference-Cited by-同舟云学术

Synthesis of 4′/5′-Spirocyclopropanated Uridine and d-Xylouridine Derivatives and Their Activity against the Human Respiratory Syncytial Virus

Published:2019-08-21 Issue:17 Volume:21 Page:6966-6971
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Köllmann Christoph,Wiechert Svenja M.¹,Jones Peter G.,Pietschmann Thomas¹,Werz Daniel B.^ORCID

Affiliation:

1. Institute for Experimental Virology, TWINCORE, Centre for Experimental and Clinical Infection Research; a Joint Venture Between the Medical School Hannover (MHH) and the Helmholtz Centre for Infection Research (HZI), Hannover, Feodor-Lynen-Str. 7, 30625 Hannover, Germany

Funder

Studienstiftung des Deutschen Volkes

Helmholtz-Alberta Initiative

Fonds der Chemischen Industrie

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b02555

Reference43 articles.

1. Acyclic nucleoside phosphonates: a key class of antiviral drugs