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

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Title Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
 
Creator KOTHA, S
RAVIKUMAR, O
MAJHI, J
 
Subject DIELS-ALDER REACTION
CLOSING METATHESIS
OLEFIN-METATHESIS
DICYCLOPENTADIENE
CATALYSTS
HETEROCYCLES
DERIVATIVES
SCAFFOLDS
SEQUENCE
LIGANDS
allylation
Beckmann rearrangement
lactams
oximes
ring-rearrangement metathesis
 
Description 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.
 
Publisher BEILSTEIN-INSTITUT
 
Date 2016-01-15T10:39:17Z
2016-01-15T10:39:17Z
2015
 
Type Article
 
Identifier BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 11,1503-1508
1860-5397
http://dx.doi.org/10.3762/bjoc.11.163
http://dspace.library.iitb.ac.in/jspui/handle/100/18368
 
Language en