Development of a Flexible and Robust Synthesis of Tetrahydrofuro[3,4-b]furan Nucleoside Analogues-Reference-Cited by-同舟云学术

Development of a Flexible and Robust Synthesis of Tetrahydrofuro[3,4-b]furan Nucleoside Analogues

Published:2021-03-23 Issue:7 Volume:86 Page:5142-5151
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Candito David A.¹^ORCID,Ye Yingchun²,Quiroz Ryan V.²^ORCID,Reutershan Michael H.²,Witter David²,Gadamsetty Surendra B.³,Li Hongming⁴,Saurí Josep⁵,Schneider Sebastian E.⁶^ORCID,Lam Yu-hong⁷^ORCID,Palte Rachel L.⁶

Affiliation:

1. Process Research and Development, Merck & Co., Inc., Boston, Massachusetts 02115, United States

2. Discovery Chemistry, Merck & Co., Inc., Boston, Massachusetts 02115, United States

3. Process Research and Development, Merck & Co., Inc., Rahway, New Jersey 07065, United States

4. External Capabilities, Merck & Co., Inc., Boston, Massachusetts 02115, United States

5. Analytical Enabling Technologies, Merck & Co., Inc., Boston, Massachusetts 02115, United States

6. Computational and Structural Chemistry, Merck & Co., Inc., Boston, Massachusetts 02115, United States

7. Computational and Structural Chemistry, Merck & Co., Inc., Rahway, New Jersey 07065, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c02969

Reference33 articles.

1. Nucleoside protein arginine methyltransferase 5 (PRMT5) inhibitors

2. Protein Arginine Methyltransferase 5 (PRMT5) as an Anticancer Target and Its Inhibitor Discovery

3. Recent Approaches in the Synthesis of Conformationally Restricted Nucleoside Analogues

4. Chemical Synthesis of Nucleoside Analogues

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