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For:	Meng J, Yu S, Wan S, Ren S, Jiang T. Synthesis, Saccharide-Binding and Anti-cancer Cell Proliferation Properties of Arylboronic Acid Derivatives of Indoquinolines: Bioactivity of Arylboronic Acid Derivatives of Indoquinolines. Chemical Biology & Drug Design 2011;78:816-25. [DOI: 10.1111/j.1747-0285.2011.01196.x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]

For:

Meng J, Yu S, Wan S, Ren S, Jiang T. Synthesis, Saccharide-Binding and Anti-cancer Cell Proliferation Properties of Arylboronic Acid Derivatives of Indoquinolines: Bioactivity of Arylboronic Acid Derivatives of Indoquinolines. Chemical Biology & Drug Design 2011;78:816-25. [DOI: 10.1111/j.1747-0285.2011.01196.x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.4] [Reference Citation Analysis]

Number	Citing Articles
1	Monforte AM, De Luca L, Buemi MR, Agharbaoui FE, Pannecouque C, Ferro S. Structural optimization of N1-aryl-benzimidazoles for the discovery of new non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains. Bioorganic & Medicinal Chemistry 2018;26:661-74. [DOI: 10.1016/j.bmc.2017.12.033] [Cited by in Crossref: 14] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
2	Ponra S, Majumdar KC. Brønsted acid-promoted synthesis of common heterocycles and related bio-active and functional molecules. RSC Adv 2016;6:37784-922. [DOI: 10.1039/c5ra27069c] [Cited by in Crossref: 32] [Cited by in F6Publishing: 33] [Article Influence: 4.6] [Reference Citation Analysis]
3	Peters JA. Interactions between boric acid derivatives and saccharides in aqueous media: Structures and stabilities of resulting esters. Coordination Chemistry Reviews 2014;268:1-22. [DOI: 10.1016/j.ccr.2014.01.016] [Cited by in Crossref: 144] [Cited by in F6Publishing: 117] [Article Influence: 16.0] [Reference Citation Analysis]
4	Yin R, Zhang M, Hao C, Wang W, Qiu P, Wan S, Zhang L, Jiang T. Different cytotoxicities and cellular localizations of novel quindoline derivatives with or without boronic acid modifications in cancer cells. Chem Commun (Camb) 2013;49:8516-8. [PMID: 23942773 DOI: 10.1039/c3cc45203d] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 1.9] [Reference Citation Analysis]
5	Wang X, Yin M, Wang W, Tu S. A Stereoselective Povarov Reaction Leading to exo-Tetrahydroindolo[3,2-c]quinoline Derivatives Catalyzed by Iodine. Eur J Org Chem 2012;2012:4811-8. [DOI: 10.1002/ejoc.201200551] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 2.4] [Reference Citation Analysis]