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For: Du HC, Bangs MC, Simmons N, Matzuk MM. Multistep Synthesis of 1,2,4-Oxadiazoles via DNA-Conjugated Aryl Nitrile Substrates. Bioconjug Chem 2019;30:1304-8. [PMID: 30964278 DOI: 10.1021/acs.bioconjchem.9b00188] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 5.7] [Reference Citation Analysis]
Number Citing Articles
1 Sauter B, Schneider L, Stress C, Gillingham D. An assessment of the mutational load caused by various reactions used in DNA encoded libraries. Bioorg Med Chem 2021;52:116508. [PMID: 34800876 DOI: 10.1016/j.bmc.2021.116508] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
2 Facchinetti V, Gomes CR, de Souza MV. Application of nitriles on the synthesis of 1,3-oxazoles, 2-oxazolines, and oxadiazoles: An update from 2014 to 2021. Tetrahedron 2021;102:132544. [DOI: 10.1016/j.tet.2021.132544] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
3 Zhang J, Li X, Wei H, Li Y, Zhang G, Li Y. Sequential DNA-Encoded Building Block Fusion for the Construction of Polysubstituted Pyrazoline Core Libraries. Org Lett 2021;23:8429-33. [PMID: 34652930 DOI: 10.1021/acs.orglett.1c03145] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 10.0] [Reference Citation Analysis]
4 Fair RJ, Walsh RT, Hupp CD. The expanding reaction toolkit for DNA-encoded libraries. Bioorg Med Chem Lett 2021;51:128339. [PMID: 34478840 DOI: 10.1016/j.bmcl.2021.128339] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 16.0] [Reference Citation Analysis]
5 Chamakuri S, Lu S, Ucisik MN, Bohren KM, Chen YC, Du HC, Faver JC, Jimmidi R, Li F, Li JY, Nyshadham P, Palmer SS, Pollet J, Qin X, Ronca SE, Sankaran B, Sharma KL, Tan Z, Versteeg L, Yu Z, Matzuk MM, Palzkill T, Young DW. DNA-encoded chemistry technology yields expedient access to SARS-CoV-2 Mpro inhibitors. Proc Natl Acad Sci U S A 2021;118:e2111172118. [PMID: 34426525 DOI: 10.1073/pnas.2111172118] [Cited by in Crossref: 11] [Cited by in F6Publishing: 14] [Article Influence: 11.0] [Reference Citation Analysis]
6 Ma F, Li J, Zhang S, Gu Y, Tan T, Chen W, Wang S, Ma P, Xu H, Yang G, Lerner RA. DNA-Encoded Libraries: Hydrazide as a Pluripotent Precursor for On-DNA Synthesis of Various Azole Derivatives. Chemistry 2021;27:8214-20. [PMID: 33811386 DOI: 10.1002/chem.202100850] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Kölmel DK, Zhu H, Flanagan ME, Sakata SK, Harris AR, Wan J, Morgan BA. Employing Photocatalysis for the Design and Preparation of DNA‐Encoded Libraries: A Case Study. Chem Rec 2021;21:616-30. [DOI: 10.1002/tcr.202000148] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
8 Shi Y, Wu Y, Yu J, Zhang W, Zhuang C. DNA-encoded libraries (DELs): a review of on-DNA chemistries and their output. RSC Adv 2021;11:2359-76. [DOI: 10.1039/d0ra09889b] [Cited by in Crossref: 32] [Cited by in F6Publishing: 35] [Article Influence: 32.0] [Reference Citation Analysis]
9 Kölmel DK, Ratnayake AS, Flanagan ME. Photoredox cross-electrophile coupling in DNA-encoded chemistry. Biochemical and Biophysical Research Communications 2020;533:201-8. [DOI: 10.1016/j.bbrc.2020.04.028] [Cited by in Crossref: 27] [Cited by in F6Publishing: 24] [Article Influence: 13.5] [Reference Citation Analysis]
10 Wen H, Ge R, Qu Y, Sun J, Shi X, Cui W, Yan H, Zhang Q, An Y, Su W, Yang H, Kuai L, Satz AL, Peng X. Synthesis of 1,2-Amino Alcohols by Photoredox-Mediated Decarboxylative Coupling of α-Amino Acids and DNA-Conjugated Carbonyls. Org Lett 2020;22:9484-9. [DOI: 10.1021/acs.orglett.0c03461] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 10.0] [Reference Citation Analysis]
11 Baykov S, Semenov A, Tarasenko M, Boyarskiy VP. Application of amidoximes for the heterocycles synthesis. Tetrahedron Letters 2020;61:152403. [DOI: 10.1016/j.tetlet.2020.152403] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
12 Li K, Liu X, Liu S, An Y, Shen Y, Sun Q, Shi X, Su W, Cui W, Duan Z, Kuai L, Yang H, Satz AL, Chen K, Jiang H, Zheng M, Peng X, Lu X. Solution-Phase DNA-Compatible Pictet-Spengler Reaction Aided by Machine Learning Building Block Filtering. iScience 2020;23:101142. [PMID: 32446221 DOI: 10.1016/j.isci.2020.101142] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
13 Götte K, Chines S, Brunschweiger A. Reaction development for DNA-encoded library technology: From evolution to revolution? Tetrahedron Letters 2020;61:151889. [DOI: 10.1016/j.tetlet.2020.151889] [Cited by in Crossref: 38] [Cited by in F6Publishing: 25] [Article Influence: 19.0] [Reference Citation Analysis]
14 Madsen D, Azevedo C, Micco I, Petersen LK, Hansen NJV. An overview of DNA-encoded libraries: A versatile tool for drug discovery. Prog Med Chem 2020;59:181-249. [PMID: 32362328 DOI: 10.1016/bs.pmch.2020.03.001] [Cited by in Crossref: 33] [Cited by in F6Publishing: 18] [Article Influence: 16.5] [Reference Citation Analysis]
15 Kölmel DK, Ratnayake AS, Flanagan ME, Tsai MH, Duan C, Song C. Photocatalytic [2 + 2] Cycloaddition in DNA-Encoded Chemistry. Org Lett 2020;22:2908-13. [PMID: 32239950 DOI: 10.1021/acs.orglett.0c00574] [Cited by in Crossref: 35] [Cited by in F6Publishing: 36] [Article Influence: 17.5] [Reference Citation Analysis]
16 Chen YC, Faver JC, Ku AF, Miklossy G, Riehle K, Bohren KM, Ucisik MN, Matzuk MM, Yu Z, Simmons N. C-N Coupling of DNA-Conjugated (Hetero)aryl Bromides and Chlorides for DNA-Encoded Chemical Library Synthesis. Bioconjug Chem 2020;31:770-80. [PMID: 32019312 DOI: 10.1021/acs.bioconjchem.9b00863] [Cited by in Crossref: 28] [Cited by in F6Publishing: 28] [Article Influence: 14.0] [Reference Citation Analysis]
17 Du HC, Matzuk MM, Chen YC. Synthesis of 5-substituted tetrazoles via DNA-conjugated nitrile. Org Biomol Chem 2020;18:9221-6. [PMID: 33174894 DOI: 10.1039/d0ob02021d] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]