BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Ganiek MA, Ivanova MV, Martin B, Knochel P. Mild Homologation of Esters through Continuous Flow Chloroacetate Claisen Reactions. Angew Chem Int Ed Engl 2018;57:17249-53. [PMID: 30290045 DOI: 10.1002/anie.201810158] [Cited by in Crossref: 19] [Cited by in F6Publishing: 8] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Harenberg JH, Weidmann N, Wiegand AJ, Hoefer CA, Annapureddy RR, Knochel P. (2-Ethylhexyl)sodium: A Hexane-Soluble Reagent for Br/Na-Exchanges and Directed Metalations in Continuous Flow. Angew Chem Int Ed Engl 2021;60:14296-301. [PMID: 33826212 DOI: 10.1002/anie.202103031] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 6.0] [Reference Citation Analysis]
2 Singh B, Ahmed J, Biswas A, Paira R, Mandal SK. Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides. J Org Chem 2021;86:7242-55. [PMID: 33949861 DOI: 10.1021/acs.joc.1c00573] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. Chem Rec 2021;21:2837-54. [PMID: 33533538 DOI: 10.1002/tcr.202000176] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Kwong A, Firth JD, Farmer TJ, O’brien P. Rapid “high” temperature batch and flow lithiation-trapping of N-Boc pyrrolidine. Tetrahedron 2021;81:131899. [DOI: 10.1016/j.tet.2020.131899] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
5 Harenberg JH, Weidmann N, Karaghiosoff K, Knochel P. Continuous Flow Sodiation of Substituted Acrylonitriles, Alkenyl Sulfides and Acrylates. Angew Chem Int Ed Engl 2021;60:731-5. [PMID: 33026681 DOI: 10.1002/anie.202012085] [Cited by in Crossref: 12] [Article Influence: 12.0] [Reference Citation Analysis]
6 Alfano AI, Brindisi M, Lange H. Flow synthesis approaches to privileged scaffolds – recent routes reviewed for green and sustainable aspects. Green Chem 2021;23:2233-92. [DOI: 10.1039/d0gc03883k] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
7 Harenberg JH, Weidmann N, Karaghiosoff K, Knochel P. Natriierung von Substituierten Acrylonitrilen, Alkenylsulfiden und Acrylaten im Kontinuierlichen Durchfluss. Angew Chem 2021;133:742-6. [DOI: 10.1002/ange.202012085] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
8 Touqeer S, Senatore R, Malik M, Urban E, Pace V. Modular and Chemoselective Strategy for Accessing (Distinct) α,α‐Dihaloketones from Weinreb Amides and Dihalomethyllithiums. Adv Synth Catal 2020;362:5056-61. [DOI: 10.1002/adsc.202001106] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
9 Harenberg JH, Weidmann N, Knochel P. Continuous-Flow Reactions Mediated by Main Group Organometallics. Synlett 2020;31:1880-7. [DOI: 10.1055/s-0040-1706536] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 3.5] [Reference Citation Analysis]
10 Power M, Alcock E, Mcglacken GP. Organolithium Bases in Flow Chemistry: A Review. Org Process Res Dev 2020;24:1814-38. [DOI: 10.1021/acs.oprd.0c00090] [Cited by in Crossref: 21] [Cited by in F6Publishing: 9] [Article Influence: 10.5] [Reference Citation Analysis]
11 Musci P, Colella M, Sivo A, Romanazzi G, Luisi R, Degennaro L. Flow Microreactor Technology for Taming Highly Reactive Chloroiodomethyllithium Carbenoid: Direct and Chemoselective Synthesis of α-Chloroaldehydes. Org Lett 2020;22:3623-7. [PMID: 32276538 DOI: 10.1021/acs.orglett.0c01085] [Cited by in Crossref: 22] [Cited by in F6Publishing: 9] [Article Influence: 11.0] [Reference Citation Analysis]
12 Yu Z, Xu Q, Liu L, Wu Z, Huang J, Lin J, Su W. Dinitration of o-toluic acid in continuous-flow: process optimization and kinetic study. J Flow Chem 2020;10:429-36. [DOI: 10.1007/s41981-020-00078-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
13 Colella M, Nagaki A, Luisi R. Flow Technology for the Genesis and Use of (Highly) Reactive Organometallic Reagents. Chemistry 2020;26:19-32. [PMID: 31498924 DOI: 10.1002/chem.201903353] [Cited by in Crossref: 43] [Cited by in F6Publishing: 17] [Article Influence: 14.3] [Reference Citation Analysis]
14 Kandasamy M, Ganesan B, Hung M, Lin W. Fast and Efficient Continuous Flow Method for the Synthesis of Ynones and Pyrazoles: Fast and Efficient Continuous Flow Method for the Synthesis of Ynones and Pyrazoles. Eur J Org Chem 2019;2019:3183-9. [DOI: 10.1002/ejoc.201900468] [Cited by in Crossref: 10] [Article Influence: 3.3] [Reference Citation Analysis]
15 Rather SA, Kumar A, Ahmed QN. Iodine–DMSO-promoted divergent reactivities of arylacetylenes. Chem Commun 2019;55:4511-4. [DOI: 10.1039/c9cc00346k] [Cited by in Crossref: 19] [Cited by in F6Publishing: 1] [Article Influence: 6.3] [Reference Citation Analysis]