Nickel-catalyzed regio- and stereoselective homo 1,4-dialkenylation of conjugated dienes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
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3. Stereo- and regioselective palladium-catalyzed 1,4-acetoxychlorination of 1,3-dienes. 1-Acetoxy-4-chloro-2-alkenes as versatile synthons in organic transformations
4. Synthesis of the major pheromonal component of the Monarch butterfly (Danaus plexippus) via palladium-catalyzed 1,4-functionalization of isoprene
5. Ziegler-type systems as catalysts for hydrosilylation: linear dimerisation with terminal acetylenes
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1. ChemInform Abstract: Nickel-Catalyzed Regio- and Stereoselective Homo 1,4-Dialkenylation of Conjugated Dienes.;ChemInform;2010-06-22
2. The Solvent-Free Addition Reaction of Allylzinc Bromide and Carbonyl Compounds;European Journal of Organic Chemistry;2009-06
3. Nickel(II)-catalyzed carbon–carbon bond formation reaction of functionalized organozinc reagents with aromatic aldehydes;Tetrahedron;2008-12
4. Functional Organonickel Reagents;Handbook of Functionalized Organometallics;2005-08-23
5. Reaction of Dienes and Allenes;Modern Organonickel Chemistry;2005-08-19
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