Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

He rearrangement of a range of N-benzyl-O-allylhydroxylamines to the corresponding N-allylhydroxylamines upon treatment with n-BuLi in THF, followed by reduction to the corresponding N-allylamines, is described. Mechanistic studies of the transformation are consistent with an intramolecular [2,3] sigmatropic rearrangement. © 2002 The Royal Society of Chemistry.

Original publication

DOI

10.1039/b205323n

Type

Journal article

Journal

Journal of the Chemical Society. Perkin Transactions 1

Publication Date

31/05/2002

Volume

2

Pages

1757 - 1765