Zobrazeno 1 - 10 of 13 pro vyhledávání: '"Kella Bennani, A."'
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Akademický článek
(2E)-2-Benzylidene-4-ethyl-3,4-dihydronaphthalen-1(2H)-one
Autor: Mohamed Akhazzane, Hafid Zouihri, A. Kella Bennani, Abdelali Kerbal, Ghali Al Houari
Publikováno v: Acta Crystallographica Section E, Vol 67, Iss 7, Pp o1700-o1700 (2011)
In the title compound, C19H18O, the exocyclic C=C double bond has an E configuration. The ethyl substituent on the cyclohexanone ring is in an axial position. The cyclohexanone ring adopts a half-chair conformation, presumably due to conjugation in t
Externí odkaz: https://doaj.org/article/2460070aa762484ab94e1f7f47e24c89
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3
CYCLOADDITION DIPOLAIRE-1,3 SUR DES OSES DE TYPE INOSITOL
Autor: Kasri, S., Kella Bennani, A., Chapleur, Y.
L’objectif de ce travail est de preparer des inositols modifies susceptibles d’etre utilisés comme precurseurs d’analogues d’IP3. En faisant appel à des réactions de cycloaddition dipolaire- 1,3. Comme dipolarophiles nous avons utilisé de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ee93e9be4109a6b13e96129e528b0987
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4
REACTION DE CYCLOADDITION DIPOLAIRE-1,3 DES ARYLNITRILOXYDES VIS A VIS DES4-ISOPROPYL-2-[(E)-ARYLIDENE]- 3,4-DIHYDRO-1(2H) NAPHTALENONES
Autor: Al Houari, G., Kella Bennani, A., Daoudi, M., Benlarbi, N., El Yazidi, M., Guarrigues, B., Kerbal, A.
La réaction de cycloaddition dipolaire-1,3 des 4-isopropyl-2-[(E)-arylidène]-3,4- dihydro-1(2H)-naphtalénones avec les arylnitriloxydes est régiospécifique et aussi diastereospecifique. L’approche du dipole se fait du cote oppose du substituan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1f7bd71bf0be38c90ee902e5f4057e4c
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5
REACTION DE CYCLOADDITION DIPOLAIRE-1,3 DES ARYLNITRILOXYDES VIS-A-VIS DES 4-ETHYL-2-[(E)-ARYLIDENE]- 3,4-DIHYDRO-1(2H) NAPHTALENONES
Autor: Akhazzane, M., Kerbal, A., Kella Bennani, A., Daoudi, M., El Yazidi, M., Guarrigues, B., Boughaleb, A., Al Houari, G.
La réaction de cycloaddition dipolaire-1,3 des 4-éthyl-2-[(E)-arylidène]-3,4-dihydro-1(2H)-naphtalénones avec les arylnitriloxydes est regiospecifique mais elle n’est que diastéréosélective. Le produit majoritaire est toujours le produit ant
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ef82f020a326714d237d8dad253b3d1
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6
PREPARATION, REDUCTION ET OUVERTURE DE DICHLOROCYCLOPROPANES DERIVES DE SUCRES
Autor: Kasri, S., Kella Bennani, A., Chapleur, Y., Gross, B.
L’action du dichlorocarbène engendré par la catalyse par transfert de phase sur des oses insaturés donne accès à des composés osidiques à motifs dichlorocyclopropaniques. La réduction de ce motif suivie d’une ouverture électrophile condu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b9182ba27e24a60282e1b9883082f3bb
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7
Synthesis of a novel tetracyclic heterocycle: 1-carboxy-13-oxo-[1,2,3]triazolo [1′,5′:4,3] [1,4]diazepino [6,7-c]chromane, using salicylaldehyde as a starting material
Autor: Az-eddine Kella-Bennani, M. Soufiaoui, Najib Bitit, Souad Fkih-Tetouani, Abdelali Kerbal
Publikováno v: Tetrahedron. 51:10923-10928
A nine-step synthesis of the potentially biologically active title compound, 9 , has been achieved starting from salicylaldehyde and involving two 13-dipolar cycloaddition reactions and a lactamisation reaction. The cis configuration of compound 9 re
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a56e0b46dbaba6e4f789b32ed69c759f
https://doi.org/10.1016/0040-4020(95)00668-x
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8
ChemInform Abstract: Synthesis of a Novel Tetracyclic Heterocycle: 1-Carboxy-13-oxo-(1,2,3) triazolo(1′,5′:4,3)(1,4)diazepino(6,7-c)chromane, Using Salicylaldehyde as a Starting Material
Autor: M. Soufiaoui, Souad Fkih-Tetouani, Najib Bitit, Abdelali Kerbal, Az-eddine Kella-Bennani
Publikováno v: ChemInform. 27
A nine-step synthesis of the potentially biologically active title compound, 9 , has been achieved starting from salicylaldehyde and involving two 13-dipolar cycloaddition reactions and a lactamisation reaction. The cis configuration of compound 9 re
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f49d7a47072d5c0aed0172776c375264
https://doi.org/10.1002/chin.199604193
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9
4-tert-Butyl-3′,4′-bis(4-methylphenyl)-3,4-dihydro-1H,4′H-spiro[naphthalene-2,5′-[1,2]oxazol]-1-one
Autor: Hafid Zouihri, A. Kella Bennani, Mohamed Akhazzane, Abdelali Kerbal, Ghali Al Houari
Publikováno v: Acta Crystallographica Section E: Structure Reports
In the title compound, C(30)H(31)NO(2), the cyclo-hexa-none ring in the naphthalene fused-ring system adopts a half-chair conformation, presumably due to conjugation of the benzene ring. The naphthalene ring system makes dihedral angles of 86.63 (7),
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c54e09bc7dd284368c3bc6e6c2caa5c
https://doi.org/10.1107/s1600536811025086
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10
(2E)-2-Benzylidene-4-ethyl-3,4-dihydronaphthalen-1(2H)-one
Autor: Hafid Zouihri, Abdelali Kerbal, A. Kella Bennani, Ghali Al Houari, Mohamed Akhazzane
Publikováno v: Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E, Vol 67, Iss 7, Pp o1700-o1700 (2011)
In the title compound, C(19)H(18)O, the exocyclic C=C double bond has an E configuration. The ethyl substituent on the cyclo-hexa-none ring is in an axial position. The cyclo-hexa-none ring adopts a half-chair conformation, presumably due to conjugat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b6e660c2400ba73295f7b6b224a7eee
https://doi.org/10.1107/s1600536811022793
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