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A flexible radical approach to 5-substituted 4,5-dihydro-3H-pyrido[4,3-b]azepin-2-ones. Some mechanistic observations on the radical cyclisation-aromatisation process
Abstract : Variously substituted novel dihydropyridoazepinones have been prepared by an intermolecular radical addition followed by a radical cyclisation on a pyridine ring. The latter process involved the use of a combination of two different peroxides, an experimental contrivance resulting from a careful product analysis and a better understanding of the cyclisation step. © 2012 Elsevier Ltd. All rights reserved.
Cited literature [3 references]
https://hal-polytechnique.archives-ouvertes.fr/hal-00949980
Contributor : Denis Roura <>
Submitted on : Monday, April 14, 2014 - 4:40:10 PM
Last modification on : Thursday, March 5, 2020 - 6:25:13 PM
Long-term archiving on: : Sunday, April 9, 2017 - 2:25:00 PM
Contributor : Denis Roura <>
Submitted on : Monday, April 14, 2014 - 4:40:10 PM
Last modification on : Thursday, March 5, 2020 - 6:25:13 PM
Long-term archiving on: : Sunday, April 9, 2017 - 2:25:00 PM
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