An Economical Route to Lamivudine Featuring a Novel Strategy for Stereospecific Assembly-Reference-Cited by-同舟云学术

An Economical Route to Lamivudine Featuring a Novel Strategy for Stereospecific Assembly

Published:2020-04-07 Issue:6 Volume:24 Page:1194-1198
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Snead David R.¹^ORCID,McQuade D. Tyler¹^ORCID,Ahmad Saeed¹,Krack Rudy¹,Stringham Rodger W.¹,Burns Justina M.¹,Abdiaj Irini¹,Gopalsamuthiram Vijayagopal¹,Nelson Ryan C.¹,Gupton B. Frank¹

Affiliation:

1. Medicines for All Institute, Virginia Commonwealth University, 737 North Fifth Street, Box 980100, Richmond, Virginia 23298, United States

Funder

Bill and Melinda Gates Foundation

National Institutes of Health

Virginia General Assembly Higher Education Equipment Trust Fund

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.oprd.0c00083

Reference42 articles.

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3. cWorld Health Organization, Data on the size of the HIV/AIDS epidemic, https://www.who.int/data/gho/data/themes/topics/topic-details/GHO/data-on-the-size-of-the-hiv-aids-epidemic (accessed 2020-04-02).

4. dWorld Atlas. Countries with the Highest Rates of HIV/AIDS. https://www.worldatlas.com/articles/countries-with-the-highest-rates-of-hiv-aids.html (accessed 2020-04-02).

5. bGoodyear, M. D.; Dwyer, P. O.; Hill, M. L.; Whitehead, A. J.; Hornby, R.; Hallet, P. Process for the diastereoselective synthesis of nucleoside analogues. US 6051709, 2000.

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