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For: Lin S, Sharma A. Recent advances in the synthesis and synthetic applications of 1,2,3-triazoles (microreview). Chem Heterocycl Comp 2018;54:314-6. [DOI: 10.1007/s10593-018-2265-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
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1 Demina MM, Medvedeva AS, Vu TD, Larina LI, Mitroshina IV, Shemyakina OA. Catalyst-free three-component synthesis of hydroxyalkyltriazolylmethylidene barbiturates. Mendeleev Communications 2019;29:655-7. [DOI: 10.1016/j.mencom.2019.11.017] [Reference Citation Analysis]
2 Ferlin F, Yetra SR, Warratz S, Vaccaro L, Ackermann L. Reusable Pd@PEG Catalyst for Aerobic Dehydrogenative C-H/C-H Arylations of 1,2,3-Triazoles. Chemistry 2019;25:11427-31. [PMID: 31306515 DOI: 10.1002/chem.201902901] [Cited by in Crossref: 15] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
3 Brandhofer T, Özdemir A, Gini A, Mancheño OG. Double Cu‐Catalyzed Direct Csp 3 −H Azidation/CuAAC Reaction: A Direct Approach towards Demanding Triazole Conjugates. Chem Eur J 2019;25:4077-86. [DOI: 10.1002/chem.201806288] [Cited by in Crossref: 16] [Cited by in F6Publishing: 7] [Article Influence: 5.3] [Reference Citation Analysis]
4 Govdi AI, Danilkina NA, Ponomarev AV, Balova IA. 1-Iodobuta-1,3-diynes in Copper-Catalyzed Azide-Alkyne Cycloaddition: A One-Step Route to 4-Ethynyl-5-iodo-1,2,3-triazoles. J Org Chem 2019;84:1925-40. [PMID: 30632741 DOI: 10.1021/acs.joc.8b02916] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
5 Lu H, Li Z. Synthesis of 1,2,3-Triazolyl-Based Ketoximes Using Calcium Carbide as an Acetylene Source: Synthesis of 1,2,3-Triazolyl-Based Ketoximes Using Calcium Carbide as an Acetylene Source. Eur J Org Chem 2020;2020:845-51. [DOI: 10.1002/ejoc.201901712] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]