Palladium catalysed mono-N-arylation of enantiopure diamines

C.G. Frost, P. Mendonça

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

The palladium catalysed arylation of amines is employed to prepare selectively a range of new, mono-N-arylated, enantiopure diamine ligands. The ligands were tested in the catalytic asymmetric transfer hydrogenation of acetophenone.
Original languageEnglish
Pages (from-to)1831-1834
Number of pages4
JournalTetrahedron: Asymmetry
Volume10
Issue number10
DOIs
Publication statusPublished - 21 May 1999

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Diamines
Palladium
diamines
palladium
Ligands
ligands
Hydrogenation
hydrogenation
Amines
amines
acetophenone

Cite this

Palladium catalysed mono-N-arylation of enantiopure diamines. / Frost, C.G.; Mendonça, P.

In: Tetrahedron: Asymmetry, Vol. 10, No. 10, 21.05.1999, p. 1831-1834.

Research output: Contribution to journalArticle

Frost, C.G. ; Mendonça, P. / Palladium catalysed mono-N-arylation of enantiopure diamines. In: Tetrahedron: Asymmetry. 1999 ; Vol. 10, No. 10. pp. 1831-1834.
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