Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ihssene Chabour"'
Autor:
H. Ali Dondas, Ihssene Chabour, José M. Sansano, Manel Chehrouri, Inmaculada Sempere, Marcos Ferrándiz-Saperas, Cristina Moreno-Cabrerizo, Adil A. Othman, M. de Gracia Retamosa
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
The Suzuki-Miyaura cross-coupling reaction using 4-amino-1,2,4-triazoles and 1,3,4-oxadiazoles-2-thiones·palladium (II) is studied. The reaction is optimized and the most appropriate catalytic complex is tested with several aryl halides, boronic aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54687f3e660e9b182fb4664b05e1b567
https://hdl.handle.net/10045/108400
https://hdl.handle.net/10045/108400
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
The reaction of diethyl phosphoramidate, conjugated aldehydes and maleimides takes place in a multicomponent sequence named phosphoramidate-aldehyde-dienophile (PAD). The reaction affords a series of N-substituted phosphoramidates in good yields with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2382452b72558063a573e628f65fc938
https://hdl.handle.net/10045/101150
https://hdl.handle.net/10045/101150
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
The multicomponent Amine-Aldehyde-Dienophile reaction is optimized employing benzyl or 4-methoxybenzylamine. The interest of the transformation consist in the synthesis of polysubstituted cyclohex-2-enylamines. The study of the scope of this AAD proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bd628582d0e95ab136832a8d0187f9c
https://hdl.handle.net/10045/88292
https://hdl.handle.net/10045/88292
Autor:
Cherif Behloul, Hind Bengliz Bey, Ihssene Chabour, Francisco Foubelo, Aicha Chouti, David Guijarro, Carmen Nájera, Miguel Yus
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
The reaction of primary, secondary, phenyl, allyl, and benzyl trityl ethers with lithium chloride in methanol at reflux led to deprotection of the trityl group affording the corresponding alcohol in good to excellent yields under mild reaction condit
Autor:
Juan Mancebo-Aracil, María de Gracia Retamosa, José M. Sansano, Ihssene Chabour, María Martín-Rodríguez, Carmen Nájera, Luis M. Castelló
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
instname
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
The asymmetric 1,3-dipolar cycloaddition of an imino ester 5 with tert-butyl acrylate is catalyzed by a dual chiral silver(I) complex formed from a chiral phosphoramidite 14 and the chiral silver(I) binolphosphate (R)-17. This reaction is selected to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e046c4c4626d5781468db93ee780b172
https://www.sciencedirect.com/science/article/pii/S0957416617303920
https://www.sciencedirect.com/science/article/pii/S0957416617303920
Autor:
Cherif Behloul, Hind Bengliz Bey, Carmen Nájera, Ihssene Chabour, Francisco Foubelo, Aicha Chouti, David Guijarro, Miguel Yus
Publikováno v:
ChemInform. 47
The reaction of primary, secondary, phenyl, allyl, and benzyl trityl ethers with lithium chloride in methanol at reflux led to deprotection of the trityl group affording the corresponding alcohol in good to excellent yields under mild reaction condit