An efficient route for the stereoselective conversion of ketones into three-carbons homologated primary E-allylamines: The palladium-catalysed reaction of vinyl triflates with N,N-di-tert-butoxycarbonyl-N-allylamine.

Tetrahedron Letters

Volumn 31, Issue 17, 1990, Pages 2463-2466

  Arcadi, A ^a   Bernocchi, E ^b   Cacchi, S ^b   Cagliot, L ^b   Marinelli, F ^a  

^a UNIVERSITY OF L'AQUILA   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE;

ARTICLE; NONHUMAN; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS;

EID: 0025265143     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)97390-8     Document Type: Article

References (24)

1. Synthesis of Primary Allylic Amines
2. N-allylation of imides catalyzed by palladium(0).
3. Palladium(0)-catalyzed azidation of allyl esters. Selective synthesis of allyl azides, primary allylamines, and related compounds
4. A Convenient One-Flask Preparation of Di-t-butyl Iminodicarbonate: A Versatile Gabriel Reagent
5. Synthesis of analogues of ?-aminobutyric acid. Part 11. Unsaturated and saturated tetronic acid [furan-2,4(3H,5H)-dione] derivatives
6. Regioselective palladium-catalyzed arylation of vinyl ethers with 4-nitrophenyl triflate. Control by addition of halide ions
7. Palladium-catalysed vinylation of organic halides under solid?liquid phase transfer conditions