On the regioselectivity of the beckmann rearrangement of cyclobutanones with o-mesitylene-sulfonylhydroxylamine. A convenient synthesis of substituted octahydrocyclopenta[b]pykroles
Journal
Tetrahedron
Journal Volume
41
Journal Issue
3
Pages
519-525
Date Issued
1985
Author(s)
Abstract
Cyclobutanones were smoothly transformed into γ-lactams by Tamura reagent. The stereoelectronic effects on the modified Beckmann rearrangenent were discussed. The extension to the synthesis of substituted octahydrocyclopenta[b]pyrroles was described. © 1985.
SDGs
Type
journal article