BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Baeten M, Maes BU. Carbon–Nitrogen Bond Formation Through Cross-Dehydrogenative Coupling Reactions. Elsevier; 2017. pp. 401-81. [DOI: 10.1016/bs.adomc.2017.04.003] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 2.2] [Reference Citation Analysis]
Number Citing Articles
1 Xu X, Amuti A, Wusiman A. Catalyst and Additive‐Free Direct Amidation/Halogenation of Tertiary Arylamines with N ‐haloimide/amides. Adv Synth Catal 2020;362:5002-8. [DOI: 10.1002/adsc.202000796] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
2 Nappi M, He C, Whitehurst WG, Chappell BGN, Gaunt MJ. Selective Reductive Elimination at Alkyl Palladium(IV) by Dissociative Ligand Ionization: Catalytic C(sp3 )-H Amination to Azetidines. Angew Chem Int Ed Engl 2018;57:3178-82. [PMID: 29380496 DOI: 10.1002/anie.201800519] [Cited by in Crossref: 32] [Cited by in F6Publishing: 24] [Article Influence: 8.0] [Reference Citation Analysis]
3 Yashwantrao G, Saha S. Sustainable strategies of C–N bond formation via Ullmann coupling employing earth abundant copper catalyst. Tetrahedron 2021;97:132406. [DOI: 10.1016/j.tet.2021.132406] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Böhmer M, Kampert F, Tan TTY, Guisado-barrios G, Peris E, Hahn FE. Ir III /Au I and Rh III /Au I Heterobimetallic Complexes as Catalysts for the Coupling of Nitrobenzene and Benzylic Alcohol. Organometallics 2018;37:4092-9. [DOI: 10.1021/acs.organomet.8b00642] [Cited by in Crossref: 27] [Cited by in F6Publishing: 8] [Article Influence: 6.8] [Reference Citation Analysis]
5 Demidov OP, Pobedinskaya DY, Avakyan EK, Amangasieva GA, Borovlev IV. S N H Arylamination of Nitroquinolines: Access to Nitro and Nitroso Derivatives of Arylaminoquinolines. Chem Heterocycl Comp 2018;54:875-86. [DOI: 10.1007/s10593-018-2368-x] [Cited by in Crossref: 3] [Article Influence: 0.8] [Reference Citation Analysis]
6 Xu XJ, Amuti A, Hu WJ, Adelibieke Q, Wusiman A. TEMPO-Promoted Mono- and Bisimidation of Tertiary Anilines: Synthesis of Symmetric and Unsymmetric N-Mannich Bases. J Org Chem 2022. [PMID: 35749377 DOI: 10.1021/acs.joc.2c00700] [Reference Citation Analysis]
7 Xia J, Huang Z, Zhou X, Yang X, Wang F, Li X. Rh(III)-Catalyzed Acceptorless Dehydrogenative Coupling of (Hetero)arenes with 2-Carboxyl Allylic Alcohols. Org Lett 2018;20:740-3. [DOI: 10.1021/acs.orglett.7b03881] [Cited by in Crossref: 35] [Cited by in F6Publishing: 27] [Article Influence: 8.8] [Reference Citation Analysis]
8 Sambiagio C, Sterckx H, Maes BUW. Electrosynthesis: A New Frontier in Aerobic Oxidation? ACS Cent Sci 2017;3:686-8. [PMID: 28776008 DOI: 10.1021/acscentsci.7b00275] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 3.6] [Reference Citation Analysis]
9 Henrion M, Smolders S, De Vos DE. Cu II /H-USY as a regenerable bifunctional catalyst for the additive-free C–H amination of azoles. Catal Sci Technol 2020;10:940-3. [DOI: 10.1039/c9cy02153a] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 Nappi M, He C, Whitehurst WG, Chappell BGN, Gaunt MJ. Selective Reductive Elimination at Alkyl Palladium(IV) by Dissociative Ligand Ionization: Catalytic C(sp 3 )−H Amination to Azetidines. Angew Chem 2018;130:3232-6. [DOI: 10.1002/ange.201800519] [Cited by in Crossref: 7] [Article Influence: 1.8] [Reference Citation Analysis]
11 Blondiaux E, Bomon J, Smoleń M, Kaval N, Lemière F, Sergeyev S, Diels L, Sels B, Maes BUW. Bio-based Aromatic Amines from Lignin-Derived Monomers. ACS Sustainable Chem Eng 2019;7:6906-16. [DOI: 10.1021/acssuschemeng.8b06467] [Cited by in Crossref: 25] [Cited by in F6Publishing: 8] [Article Influence: 8.3] [Reference Citation Analysis]