New synthesis of 10-alkoxy-5-H-dibenz[b,f]azepines

Article abstract of DOI:10.1080/00397919408012646

The reaction of 5-acetyl-5H-dibenz[b,f]azepines with sodium-hypochlorite led to the 5-acetyl-10,11-epoxy-10,11-dihydro-5H-dibenz[b,f]azepine (1). The lithium iodide induced rearrangement of 1 gave the keton 2 which was reacted with trialkyl-orthoformates leading to the vinyl ethers 3a,b.

Full text of DOI:10.1080/00397919408012646

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Synthetic Communications: An
International Journal for Rapid
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New Synthesis of 10-
Alkoxy-5H-dibenz[b,f]azepines
Ferenc Haász a & Vilmos Galamb a
a Alkaloida Chemical Company Ltd. , H4440,
Tiszavasvári, Hungary
Published online: 23 Sep 2006.
To cite this article: Ferenc Haász & Vilmos Galamb (1994) New Synthesis of 10-
Alkoxy-5H-dibenz[b,f]azepines, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 24:5, 683-687, DOI:
10.1080/00397919408012646
To link to this article: http://dx.doi.org/10.1080/00397919408012646
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