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(searched for: doi:10.5155/eurjchem.6.4.394-403.1297)
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Nguyen Thi Hoa, Nguyen Quang Trung, Nguyen Minh Thong, Adam Mechler,
Published: 6 October 2021
Chemical Physics Letters, Volume 784; https://doi.org/10.1016/j.cplett.2021.139105

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, Le Thi Ngoc Van, Nguyen Thi Hoa,
Published: 7 January 2021
Polymer Degradation and Stability, Volume 185; https://doi.org/10.1016/j.polymdegradstab.2021.109483

The publisher has not yet granted permission to display this abstract.
Published: 9 October 2020
Synthetic Communications, Volume 50, pp 3845-3853; https://doi.org/10.1080/00397911.2020.1828925

Abstract:
Syntheses of pyridazine derivatives of dibenzoazepine, starting from N-substituted-dibenzoazepines, are reported here for the first time. In the reaction sequence, N-substitute dibenzoazepine derivatives were synthesized and then, examined inverse electron demand Diels–Alder (IEDDA) reactions between N-substituted dibenzoazepine derivatives and tetrazines. While in some reactions, targeted products were obtained using phenyliodo-bis(trifluoroacetate) (PIFA), in other reactions, they were obtained directly with tetrazines which also behaved as the oxidizing agent. Structures of these compounds were fully characterized by NMR, IR, and HRMS spectroscopic techniques. Graphical Abstract
Maria Aqeel Khan, Farhana Batool, Asma Khatoon, Rabia Sadiq, Sher Rahman,
European Journal of Chemistry, Volume 8, pp 179-182; https://doi.org/10.5155/eurjchem.8.2.179-182.1567

Abstract:
Dibenzoazepine represents an important class of heterocycles, exhibiting potent antidepressant and anticonvulsant activities. Beside, various modifications on this nucleus, amide analogs at N-5 position showed potent antidepressant activities. A previously reported method for the synthesis of benzamide analogs of dibenzoazepine use hazardous and toxic solvents. Herein, we report a new, efficient and solvent-free green method for the synthesis of dibenzoazepine benzamides (6-21).
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