Výsledky vyhledávání - "Karin Monnier-Jobé"

Synthesis of highly substituted spiropyrrolidines via 1, 3-dipolar cycloaddition reaction of N-metalated azomethine ylides. A new access to spiropyrroline derivatives

Autor: Chourouk Mhiri, Fadwa Rouatbi, Sarra Boudriga, Moheddine Askri, Kabula Ciamal, Michael Knorr, Karin Monnier-Jobé, Abderrahim Khatyr, Yoann Rousselin, Marek M. Kubicki

Publikováno v: Mediterranean Journal of Chemistry
Mediterranean Journal of Chemistry, Mediterranean Journal of Chemistry, 2015, 4 (1), pp.30-50
Mediterranean Journal of Chemistry, Vol 4, Iss 1, Pp 30-50 (2015)

1,3-dipolar cycloaddition of (E)-arylidene-(2H)-indanones 1 (Ar = Ph, p-MeC6H4, p-MeOC6H4, p-ClC6H4) and (E)-2-arylidene-(2H)-tetralones 2 (Ar = Ph, p-MeC6H4, p-MeOC6H4, p-ClC6H4) to N-metalated azomethine ylides 3 generated from methyl N-arylidenegl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9648084d5957cae9860f10f44bb485da
https://hal.science/hal-01277418

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Regio- and stereoselective 1,3-dipolar cycloaddition of C-aryl-N-phenylnitrones over (E)-arylidene-(2H)-indan-1-ones: synthesis of highly substituted novel spiro-isoxazolidines

Autor: Karin Monnier-Jobé, Mohamed El Baker Rammah, Nadia Wannassi, Mohamed Mehdi Rammah, Sarra Boudriga, Kabula Ciamala, Michael Knorr, Yoann Rousselin, Marek M. Kubicki, Mironel Enescu

Publikováno v: Heterocycles
Heterocycles, The Japan Institute of Heterocyclic Chemistry, 2010, 81 (12), pp.2749-2462. ⟨10.3987/COM-10-12022⟩

Synthesis of a series of novel spiro-isoxazolidines has been accomplished in good yields by regio- and diastereoselective 1,3-dipolar cycloaddition of (E)-2-arylidene-(2H)-indan-1-ones 1a-d to C-aryl-N-phenylnitrones 2e-h. The structure of the spiro-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64a7c6f87e2a36ba91dc5794753df586
https://hal.archives-ouvertes.fr/hal-00556952

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