Regioselective Allylic Amination Catalyzed by Iron Salts

DOI: 10.1016/S0040-4039(00)78485-1

Source and publish data:

Tetrahedron Letters p. 8739 - 8742 (1994)

Update date:2022-08-05

Topics:

Authors:

Sristava, Radhey S.

Nicholas, Kenneth M.

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Article abstract of DOI:10.1016/S0040-4039(00)78485-1

Alkenes react with phenylhydroxylamine in the presence of Fe(II) and Fe(III) salts to produce N-phenyl-N-allyl amines in moderate to good yields.Unsymmetrical substrates react with high regioselectivity giving the products of double bond transition.

Full text of DOI:10.1016/S0040-4039(00)78485-1

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