Room-Temperature Isolation of Palladium(II) Organocarbonyl Intermediates in the Synthesis of Eight-Membered Lactams after Alkyne/CO Sequential Insertions
Author:
Affiliation:
1. Grupo de Quı́mica Organometálica, Departamento de Quı́mica Inorgánica, Facultad de Quı́mica, Universidad de Murcia, E-30071 Murcia, Spain
2. SAI, Universidad de Murcia, E-30071 Murcia, Spain
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om301241n
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3. Reactivity of cyclopalladated compounds. Part 17. Influence of the donor atom in metallacyclic rings on the insertion of tert-butyl isocyanide and carbon monoxide into their palladium-carbon bonds. X-ray molecular structure of cyclo-[Pd(.eta.-(CN)-.mu.-C(C6H4CH2SMe):NBu-tert)Br]2
4. Mechanistic studies of the palladium-catalyzed reaction of methanol with bromobenzene and carbon monoxide to produce methyl benzoate. 1. Stoichiometric study
5. Reactions of cyclopalladated compounds. Part 24. Reactivity of the Pd–C bond of cyclopalladated compounds towards isocyanides and carbon monoxide. Role of the donor group
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