Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/3887
Title: Metal-Free Ring Opening Cyclization of Cyclopropane Carbaldehydes and N-Benzyl Anilines: An Eco-Friendly Access to Functionalized Benzo[b]azepine Derivatives
Authors: Dey, R.
Banerjee, P.
Keywords: benzo[b]azepine
cyclopropane carbaldehyde
metal-free ring opening cyclization
N-benzyl aniline
Issue Date: 25-Aug-2022
Abstract: Herein, we report a p-toluenesulfonic acid (PTSA) initiated mild and user-friendly ring opening/domino ring opening cyclization reaction (depends on substituent present in N-benzyl aniline) of cyclopropane carbaldehyde and N-benzyl aniline towards the formation of substituted 4-amino butanal/2,3-dihydro-1H-benzo[b]azepine. The product dihydro-1H-benzo[b]azepine was also converted into the corresponding tetrahydro-1H-benzo[b]azepine.
URI: http://localhost:8080/xmlui/handle/123456789/3887
Appears in Collections:Year-2019

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