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Bai J, Li S, Zhu R, Li Y, Li W. B(2)(OH)(4)-Mediated Reductive Transamidation of N-Acyl Benzotriazoles with Nitro Compounds En Route to Aqueous Amide Synthesis. J Org Chem 2023;88:3714-23. [PMID: 36888556 DOI: 10.1021/acs.joc.2c02995] [Reference Citation Analysis]
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| 2 |
Panjacharam P, Ulabala V, Jayakumar J, Rajasekhara Reddy S. Emerging trends in the sustainable synthesis of N-N bond bearing organic scaffolds. Org Biomol Chem 2023. [PMID: 36883312 DOI: 10.1039/d3ob00300k] [Reference Citation Analysis]
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| 3 |
Liu X, Zhang X, Zhang G, Sun S, Li D. A Deeper Understanding of H2 Evolution Entirely from Water via Diborane Hydrolysis. ACS Materials Lett 2023. [DOI: 10.1021/acsmaterialslett.2c01046] [Reference Citation Analysis]
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| 4 |
Zhao G, Wang H, Luo J, He X, Xiong F, Li Y, Zhang G, Li Y. Multicomponent DNA-Compatible Synthesis of an Annelated Benzodiazepine Scaffold for Focused Chemical Libraries. Org Lett 2023;25:665-70. [PMID: 36693020 DOI: 10.1021/acs.orglett.2c04293] [Reference Citation Analysis]
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| 5 |
Gao Y, Sun Y, Zhao G, Zhang G, Li Y, Li Y. On-DNA Synthesis of Functionalized 4H-Pyran Scaffolds for Focused DNA-Encoded Chemical Libraries. Org Lett 2022. [PMID: 36053053 DOI: 10.1021/acs.orglett.2c02714] [Reference Citation Analysis]
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| 6 |
Gao Y, Sun Y, Fang X, Zhao G, Li X, Zhang G, Li Y, Li Y. Development of on-DNA vinyl sulfone synthesis for DNA-encoded chemical libraries. Org Chem Front . [DOI: 10.1039/d2qo00881e] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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Bhattacharjee S, Laru S, Hajra A. Hypervalent iodine(iii)-mediated oxidative dearomatization of 2H-indazoles towards indazolyl indazolones. Org Biomol Chem 2022. [DOI: 10.1039/d2ob01776h] [Reference Citation Analysis]
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| 8 |
Qi J, Liu S, Seydimemet M, Wang X, Lu X. A General Set of DNA-Compatible Reactions for Preparing DNA-Tagged Multisubstituted Pyrroles. Bioconjug Chem 2021;32:2290-4. [PMID: 34699185 DOI: 10.1021/acs.bioconjchem.1c00427] [Reference Citation Analysis]
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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: 8.0] [Reference Citation Analysis]
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| 10 |
Wu R, Du T, Sun W, Shaginian A, Gao S, Li J, Wan J, Liu G. Functionalization of DNA-Tagged Alkenes Enabled by Visible-Light-Induced C–H Activation of N -Aryl Tertiary Amines. Org Lett 2021;23:3486-90. [DOI: 10.1021/acs.orglett.1c00924] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
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| 11 |
Park JH, Wang HM, Shin MH, Lim H. Synthesis of a DNA‐Encoded Library of Pyrrolo[2,3 ‐d ]pyrimidines. Bull Korean Chem Soc 2021;42:691-8. [DOI: 10.1002/bkcs.12243] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
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| 12 |
Wu R, Gao S, Du T, Cai K, Cheng X, Fan J, Feng J, Shaginian A, Li J, Wan J, Liu G. Exploring Aldol Reactions on DNA and Applications to Produce Diverse Structures: An Example of Expanding Chemical Space of DNA-Encoded Compounds by Diversity-Oriented Synthesis. Chem Asian J 2020;15:4033-7. [PMID: 33119184 DOI: 10.1002/asia.202001105] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
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