Cu(I)-catalyzed allylic amination of olefins
โ Scribed by Gregg A Hogan; August A Gallo; Kenneth M Nicholas; Radhey S Srivastava
- Book ID
- 104252562
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 272 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
The copper(I) complex [Cu(CH 3 CN) 4 ]PF 6 catalyzes the allylic amination of alkenes by aryl hydroxylamine in fair to moderate yields. Unsymmetrical alkenes react with high regioselectivity with N-functionalization occuring at the less substituted vinylic carbon. Trapping experiments indicate that free PhNO is not an intermediate in these reactions.
๐ SIMILAR VOLUMES
Allylic hydrocarbons are selectively converted to the corresponding allyl amines in good to excellent yield by reaction with aryl hydroxylamines catalyzed by a 1:1 mixture of CuCl and CuCl 2 (10 mol %). Under these conditions unsymmetrical olefins react highly regioselectively with N-functionalizati
## Abstract Unsymmetrical olefins react highly regioselectively with phenyl hydroxylamine.
The transition metal catalyzed allylic amination of olefins are studied. A screening of catalysts known for the intermediacy of PhNO in the amination of alkene with phenylhydroxylamine reveals that the hydrated copper salt in conjugation with copper powder as reductant has the best catalytic propert