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000778406 0247_ $$a10.1007/978-3-319-49784-6$$2doi
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000778406 24500 $$aNi- and Fe-based cross-coupling reactions /$$cArkaitz Correa, editor ; with contributions from Lutz Ackermann [and more].
000778406 264_1 $$aCham, Switzerland :$$bSpringer,$$c[2017]
000778406 300__ $$a1 online resource.
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000778406 4901_ $$aTopics in current chemistry collections
000778406 5050_ $$aEditorial; Ni-Catalyzed C -- C Couplings Using Alkyl Electrophiles; Abstract; Introduction; Reaction of Alkyl Electrophiles; C(sp3) -- C(sp3) Coupling Reaction; C(sp3) -- C(sp2) Coupling Reaction; C(sp3) -- C(sp) Coupling Reaction; Mechanisms; Ni/Electron Deficient pi -Ligand System; Ni/1,3-Butadiene Catalytic System; Ni/nitrogen Based Ligand System; Asymmetric Coupling Reaction of Alkyl Electrophiles; Applications; Conclusion and Outlook; References; Photoredox Catalysis in Nickel-Catalyzed Cross-Coupling; Abstract; Introduction; Cross-Coupling with Organotrifluoroborates
000778406 5058_ $$aCross-Coupling with SilicatesDecarboxylative Cross-Coupling; Miscellaneous; Conclusions and Outlook; Acknowledgments; References; Nickel-Catalyzed Reductive Couplings; Abstract; Introduction; Reductive Coupling of Two Electrophiles; Cross-Coupling of Two C(sp3) -- Electrophiles; Ni-Catalyzed Coupling Between Unactivated C(sp3) -- and C(sp3) -- Electrophiles; Coupling with Activated Alkyl Electrophiles; Cyclization of Dielectrophiles; Reductive Arylation and Vinylation of Alkyl Halides; Ni-Catalyzed Reductive Arylation of Alkyl Halides; Vinylation of Unactivated Alkyl Halides
000778406 5058_ $$aCoupling of Activated Alkyl ElectrophilesKetone Synthesis; Carboxylation of Alkyl Halides with CO2; Enantioselective C(sp3) -- C(sp2) Bond Formation; Addition of Allyl and Benzyl Groups to Carbonyl Compounds; Reductive Coupling of Aryl Halides with Other C(sp2) -- Electrophiles; Formation of Biaryl Compounds; Coupling of Aryl Electrophiles with Carbonyl Compounds; Coupling of Aryl Electrophiles with Michael Acceptors; Conclusions; Acknowledgments; References; Ni- and Fe-catalyzed Carboxylation of Unsaturated Hydrocarbons with CO2; Abstract; Introduction; Carboxylation of Alkynes
000778406 5058_ $$aStoichiometric ProcessesCatalytic Carboxylation of Alkynes; Reductive Carboxylation of Alkynes; Catalytic Hydrocarboxylation of Alkynes; Carboxylation of Alkenes; Stoichiometric Processes Involving Alkenes; Catalytic Carboxylation of Olefins with CO2; Catalytic Reductive Carboxylation of Alkenes with CO2; Carboxylation of Ethylene with CO2 En Route to Acrylate Derivatives; Carboxylation of Multiple Unsaturated Systems; Allenes; Stoichiometric Reactions Using Allenes; Catalytic Processes Involving Allenes as Substrates; Dienes and Related Unsaturated Systems; Stoichiometric Studies
000778406 5058_ $$aCatalytic Carboxylation of 1,3-dienesConclusions and Future Perspective; Acknowledgments; References; Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C -- O Bond Activation; Abstract; Introduction; Cross-Coupling Reactions of Aryl Esters and Carbamates; Kumada-Tamao-Corriu Type Reactions; Negishi Type Reactions; Suzuki-Miyaura Type Reactions; Cross-Coupling with C -- H Bonds; Carbon -- Heteroatom Bond-Forming Reactions; Miscellaneous; Cross-Coupling Reactions of Aryl Ethers; Kumada-Tamao-Corriu Type Reactions; Negishi Type Reactions; Suzuki-Miyaura Type Reactions
000778406 506__ $$aAccess limited to authorized users.
000778406 520__ $$aThe series Topics in Current Chemistry Collections presents critical reviews from the journal Topics in Current Chemistry organized in topical volumes. The scope of coverage is all areas of chemical science including the interfaces with related disciplines such as biology, medicine and materials science. The goal of each thematic volume is to give the non-specialist reader, whether in academia or industry, a comprehensive insight into an area where new research is emerging which is of interest to a larger scientific audience. Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field.
000778406 650_0 $$aNickel catalysts.
000778406 650_0 $$aIron catalysts.
000778406 7001_ $$aCorrea, Arkaitz,$$eeditor.
000778406 77608 $$iPrint version:$$z3319497839$$z9783319497839$$w(OCoLC)961408768
000778406 830_0 $$aTopics in current chemistry collections.
000778406 852__ $$bebk
000778406 85640 $$3SpringerLink$$uhttps://univsouthin.idm.oclc.org/login?url=http://link.springer.com/10.1007/978-3-319-49784-6$$zOnline Access$$91397441.1
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