BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Brandão P, Pineiro M, Pinho e Melo TMVD. Flow Chemistry: Towards A More Sustainable Heterocyclic Synthesis: Flow Chemistry: Towards A More Sustainable Heterocyclic Synthesis. Eur J Org Chem 2019;2019:7188-217. [DOI: 10.1002/ejoc.201901335] [Cited by in Crossref: 24] [Cited by in F6Publishing: 23] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Brandão P, Pineiro M, M.v.d. Pinho e Melo T. Flow Chemistry: Sequential Flow Processes for the Synthesis of Heterocycles. In: Pinho e Melo TM, Pineiro M, editors. Heterocycles. Wiley; 2022. pp. 371-99. [DOI: 10.1002/9783527832002.ch11] [Reference Citation Analysis]
2 Donnelly K, Baumann M. Flow synthesis of oxadiazoles coupled with sequential in-line extraction and chromatography. Beilstein J Org Chem 2022;18:232-9. [DOI: 10.3762/bjoc.18.27] [Reference Citation Analysis]
3 Gambacorta G, Baxendale IR. Continuous-Flow Hofmann Rearrangement Using Trichloroisocyanuric Acid for the Preparation of 2-Benzoxazolinone. Org Process Res Dev . [DOI: 10.1021/acs.oprd.1c00440] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Wan L, Jiang M, Cheng D, Liu M, Chen F. Continuous flow technology-a tool for safer oxidation chemistry. React Chem Eng . [DOI: 10.1039/d1re00520k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
5 Belen’kii LI, Gazieva GA, Evdokimenkova YB, Soboleva NO. The literature of heterocyclic chemistry, Part XIX, 2019. Advances in Heterocyclic Chemistry 2022. [DOI: 10.1016/bs.aihch.2021.09.002] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Alves AJS, Silvestre JAD, Pinho e Melo TMVD. Synthesis of novel chiral spiro-β-lactams from nitrile oxides and 6-(Z)-(benzoylmethylene)penicillanate: batch, microwave-induced and continuous flow methodologies. RSC Adv 2022;12:30879-30891. [DOI: 10.1039/d2ra04848e] [Reference Citation Analysis]
7 Lopatka P, Gavenda M, Markovič M, Koóš P, Gracza T. Flow Pd(II)-Catalysed Carbonylative Cyclisation in the Total Synthesis of Jaspine B. Catalysts 2021;11:1513. [DOI: 10.3390/catal11121513] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Goel S, Khulbe M, Aggarwal A, Kathuria A. Recent advances in continuous flow synthesis of heterocycles. Mol Divers 2021. [PMID: 34661798 DOI: 10.1007/s11030-021-10338-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
9 Biedermann D, Hurtová M, Benada O, Valentová K, Biedermannová L, Křen V. Continuous Diastereomeric Kinetic Resolution—Silybins A and B. Catalysts 2021;11:1106. [DOI: 10.3390/catal11091106] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
10 Aghapoor K, Mohsenzadeh F, Darabi HR, Sayahi H. Crystalline salicylic acid as an efficient catalyst for ultrafast Paal–Knorr pyrrole synthesis under microwave induction. J Chem Sci 2021;133. [DOI: 10.1007/s12039-021-01891-9] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Chen L, lin Z, Zhang X, Tan L, Zhang M, Li Y. Catalyst-free visible-light induced synthesis of nitrogen- and oxygen-containing heterocycles from 1,3-diketones. Environ Chem Lett 2021;19:1831-7. [DOI: 10.1007/s10311-020-01150-2] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
12 Plumet J. 1,3-Dipolar Cycloaddition Reactions of Nitrile Oxides under "Non-Conventional" Conditions: Green Solvents, Irradiation, and Continuous Flow. Chempluschem 2020;85:2252-71. [PMID: 33044044 DOI: 10.1002/cplu.202000448] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
13 Moorefield CN, Newkome GR. Eight-membered and larger rings. Progress in Heterocyclic Chemistry 2021. [DOI: 10.1016/b978-0-323-89812-6.00017-1] [Reference Citation Analysis]
14 Dias KDA, Pereira Junior MVP, Andrade LH. Benzoic acid resin (BAR): a heterogeneous redox organocatalyst for continuous flow synthesis of benzoquinones from β-O-4 lignin models. Green Chem 2021;23:2308-16. [DOI: 10.1039/d0gc04231e] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Díaz-ortiz Á, de la Hoz A. Green Aspects of Flow Chemistry for Drug Discovery. Topics in Medicinal Chemistry 2021. [DOI: 10.1007/7355_2021_111] [Reference Citation Analysis]
16 Margi NH, Yadav GD. Design of a novel dual function membrane microreactor for liquid–liquid–liquid phase transfer catalysed reaction: selective synthesis of 1-naphthyl glycidyl ether. React Chem Eng 2021;6:858-67. [DOI: 10.1039/d1re00030f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Tsiasioti A, Tzanavaras PD. Determination of glutathione and glutathione disulfide using zone fluidics and fluorimetric detection. Talanta 2021;222:121559. [DOI: 10.1016/j.talanta.2020.121559] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
18 Lefebvre C, Hoffmann N. Photochemical rearrangements in organic synthesis and the concept of the photon as a traceless reagent. Nontraditional Activation Methods in Green and Sustainable Applications 2021. [DOI: 10.1016/b978-0-12-819009-8.00008-6] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
19 García-Lacuna J, Domínguez G, Pérez-Castells J. Flow Chemistry for Cycloaddition Reactions. ChemSusChem 2020;13:5138-63. [PMID: 32662578 DOI: 10.1002/cssc.202001372] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
20 Nascimento VR, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams. Org Biomol Chem 2020;18:5458-65. [PMID: 32639487 DOI: 10.1039/d0ob01104e] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
21 Gérardy R, Debecker DP, Estager J, Luis P, Monbaliu JM. Continuous Flow Upgrading of Selected C2-C6 Platform Chemicals Derived from Biomass. Chem Rev 2020;120:7219-347. [PMID: 32667196 DOI: 10.1021/acs.chemrev.9b00846] [Cited by in Crossref: 110] [Cited by in F6Publishing: 117] [Article Influence: 55.0] [Reference Citation Analysis]
22 Higashio K, Katsuragi S, Kundu D, Adebar N, Plass C, Kühn F, Gröger H, Akai S. Continuous‐Flow Dynamic Kinetic Resolution of Racemic Alcohols by Lipase–Oxovanadium Cocatalysis. Eur J Org Chem 2020;2020:1961-7. [DOI: 10.1002/ejoc.202000186] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]