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Nickel Catalyzed Reactions of Nucleophiles with Unactivated and Partially Activated Olefins and Acetylenes

✍ Scribed by Ioannis N. Houpis; Jaemoon Lee


Book ID
104209772
Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
920 KB
Volume
56
Category
Article
ISSN
0040-4020

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✦ Synopsis


Introduction 817 2. Addition of C-Ni Species to Unactivated Olefins and Acetylenes 818 2.1. Reaction of olefins and acetylenes with external organometallics 818 2.2. Sequential additions of C-Ni species to olefins and acetylenes 820 2.3. Ni-catalyzed Zn-halogen exchange of alkyl halides and addition to olefins and acetylenes 824 2.4. Addition to olefins and acetylenes of C-Ni species generated from chemical reduction of halides 826 2.5. Addition to olefins and acetylenes of C-Ni species generated from electrochemical reduction of halides 829 3. Addition of HCN to Acetylenes and Olefins 829 3.1. Addition of HCN to acetylenes 829 3.2. Ni-catalyzed addition of HCN to olefins 830 3.3. Ni-catalyzed asymmetric hydrovinylation reaction 831 4. Substitution of Allylic Systems by Organometallics 833 4.1. Substitution of allyl ethers, carbonates and amines 833 4.2. Substitution of allyl halides 837 5. [nΟ©m] Cycloadditions 837 6. Ni-Catalyzed Conjugate Addition Reactions 838 6.1. Alkyl organo-nickel additions to enones 838 6.2. Ni-catalyzed additions to enones by -ate complexes 841 7. Conclusion


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Nickel-Catalyzed Electrochemical Arylati
✍ Sylvie Condon; Daniel DuprΓ©; Gilles Falgayrac; Jean-Yves NΓ©dΓ©lec πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 311 KB πŸ‘ 2 views

Nickel-catalyzed electrochemical conjugate additions of substituted aryl bromides to activated olefins under recently optimized reaction conditions are reported. Good to high yields were obtained, whatever the nature of substituents in the meta-and para-positions of the benzene ring. In the or-