The title process comprises a method which does not employ 9,10-unsatd. precursors. Thus, 5-cyano-10,11-dihydro-5H-dibenz[b,f]azepine was brominated and the product hydroxylated to give 5-cyano-10 hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine which was converted to the title compd

5-Cyano-10-hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine, processes for its preparation and for its conversion into 5-carbamoyl-10-oxo-10,11-dihydro-5H-dibenz[b,f]azepine or into 5-carbamoyl-5H-dibenz[b,f]azepine

CITTERIO, ATTILIO;
2001-01-01

Abstract

The title process comprises a method which does not employ 9,10-unsatd. precursors. Thus, 5-cyano-10,11-dihydro-5H-dibenz[b,f]azepine was brominated and the product hydroxylated to give 5-cyano-10 hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine which was converted to the title compd
2001
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/533027
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