BECKMANN REARRANGEMENT OF OXIME SULFONATES BY GRIGNARD REAGENTS

DOI: 10.1016/S0040-4039(00)87624-8

Source and publish data:

Tetrahedron Letters p. 3395 - 3396 (1982)

Update date:2022-08-05

Topics:

Authors:

Hattori, Kazunobu

Maruoka, Keiji

Yamamoto, Hisashi

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Article abstract of DOI:10.1016/S0040-4039(00)87624-8

The Beckmann rearrangement of oxime sulfonates by Grignard reagents provides an efficient and general entry to α-alkyl- and α,α-dialkylamines in good yields.

Full text of DOI:10.1016/S0040-4039(00)87624-8

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