339166-14-2Relevant academic research and scientific papers
Synthesis of some new monocyclic β-lactams as antimalarial agents
Jarrahpour, Aliasghar,Aye, Malihe,Sinou, Vronique,Latour, Christine,Brunel, Jean Michel
, p. 2083 - 2092 (2015)
A series of new monocyclic β-lactams bearing several methoxy groups and possessing a similar meticillin structure was prepared by the ketene-imine [2+2] cycloaddition reaction (Staudinger reaction). The cycloaddition reaction was found to be totally diast
Metal-Free Ring Opening Cyclization of Cyclopropane Carbaldehydes and N-Benzyl Anilines: An Eco-Friendly Access to Functionalized Benzo[b]azepine Derivatives
Dey, Raghunath,Banerjee, Prabal
supporting information, p. 2849 - 2854 (2019/04/26)
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. (Figure presented.).
NOVEL BIS-AMIDE DERIVATIVE AND USE THEREOF
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Paragraph 0121, (2016/08/29)
The present invention relates to a novel bis-amide derivative compound or a pharmaceutically acceptable salt thereof; a method of preparation thereof; and a pharmaceutical composition for preventing or treating diseases caused by hepatitis C virus infecti
Synthesis of optically active 1,2,3-trisubstituted azetidines employing an organocatalytic approach with L-proline
Amongero, Marcela,Kaufman, Teodoro S.
, p. 1924 - 1927 (2013/04/10)
A concise organocatalytic approach towards optically active 1,2,3-trisubstituted azetidines, including a study of the scope and limitations of the synthetic sequence, is reported. The synthesis comprises the one-pot L-proline promoted three-component reac
