Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Diana Gitis"'
Publikováno v:
Organic Process Research & Development. 7:109-114
Heterogeneous Pd-catalyzed coupling reaction of substituted halobenzenes to biphenyls is performed effectively in different organic solvents using an alcohol as the reducing agent in the presence o...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f414f18dd5169a28a4716c3bb5bfb71
https://doi.org/10.1021/op015519+
https://doi.org/10.1021/op015519+
Autor:
Mubeen Baidossi, Diana Gitis, Gadi Rothenberg, Datta E. Ponde, Yoel Sasson, Sudip Mukhopadhyay
Publikováno v:
Scopus-Elsevier
A novel and simple protocol for the reductive cross-coupling of halobenzenes (PhX; X = Cl, Br, I) with pyridine is presented, using catalytic (0.5 mol%) palladium on carbon. Catalyst regeneration is effected using molecular hydrogen generated in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25b6af29d87623c5141638f6a5b38000
https://doi.org/10.1039/b004116p
https://doi.org/10.1039/b004116p
Publikováno v:
Scopus-Elsevier
Coupling reactions of substituted chlorobenzenes to biphenyls catalyzed by palladium on carbon are performed in water using sodium hydroxide and sodium formate in the presence of a surface active agent. Thus, chlorobenzene, p-chloro-o-xylene, p-chlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b141fff1524e378dcbd1e3d2c28551c
https://doi.org/10.1039/a905625d
https://doi.org/10.1039/a905625d
Publikováno v:
ChemInform. 31
Coupling reactions of substituted chlorobenzenes to biphenyls catalyzed by palladium on carbon are performed in water using sodium hydroxide and sodium formate in the presence of a surface active agent. Thus, chlorobenzene, p-chloro-o-xylene, p-chlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d8142c6a4621e4d748c9aa8e8f372c5
https://doi.org/10.1002/chin.200008046
https://doi.org/10.1002/chin.200008046
Autor:
Mubeen Baidossi, Gadi Rothenberg, Sudip Mukhopadhyay, Diana Gitis, Yoel Sasson, Datta E. Ponde
Publikováno v:
ChemInform. 31
A novel and simple protocol for the reductive cross-coupling of halobenzenes (PhX; X = Cl, Br, I) with pyridine is presented, using catalytic (0.5 mol%) palladium on carbon. Catalyst regeneration is effected using molecular hydrogen generated in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33cdd6d378a0a339ac1c84b477e60569
https://doi.org/10.1002/chin.200049138
https://doi.org/10.1002/chin.200049138
Publikováno v:
Scopus-Elsevier
[reaction: see text] Kinetics and process parameters of coupling and hydro-dehalogenation reactions of chloroaryls are studied in the presence of zinc, water, and catalytic Pd/C. Good yields are obtained for the coupling of chlorobenzene, 4-chlorotol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cbc914c0033d90ae2da543b36e733d9
https://pubmed.ncbi.nlm.nih.gov/10814284
https://pubmed.ncbi.nlm.nih.gov/10814284
Publikováno v:
The Journal of organic chemistry. 65(10)
The in situ combination of oxidative coupling of benzene to biphenyl and reductive coupling of chlorobenzene (also to biphenyl) using palladium catalysts (Pd(2+)/Pd(0)) is described. In each cycle, the reductive process regenerates the catalyst for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22835998ab49c03c79543999851ae717
https://pubmed.ncbi.nlm.nih.gov/10814203
https://pubmed.ncbi.nlm.nih.gov/10814203