Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps

A tricyclic lactam is reported in a four step synthesis sequence via Beckmann rearrangement and ring-rearrangement metathesis as key steps. Here, we used a simple starting material such as dicyclopentadiene.

Bibliographic Details
Published in:	Beilstein Journal of Organic Chemistry
Main Authors:	Sambasivarao Kotha, Ongolu Ravikumar, Jadab Majhi
Format:	Article
Language:	English
Published:	Beilstein-Institut 2015-08-01
Subjects:	allylation Beckmann rearrangement lactams oximes ring-rearrangement metathesis
Online Access:	https://doi.org/10.3762/bjoc.11.163

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