Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Thouraya Gmiza"'
Autor:
Jameleddine, Khiari1 (AUTHOR), Thouraya, Gmiza1 (AUTHOR), Adnen, Hadj AyedMed1 (AUTHOR), Hassine Béchir, Ben1 (AUTHOR) bechirbenhassine@yahoo.fr
Publikováno v:
Synthetic Communications. 2007, Vol. 37 Issue 22, p3939-3944. 6p. 1 Diagram, 1 Chart.
Autor:
Thouraya, Gmiza1 (AUTHOR), Jameleddine, Khiari1 (AUTHOR), Adnen, HadjAyed Med1 (AUTHOR), Béchir, BenHassine1 (AUTHOR) bechirbenhassine@yahoo.fr
Publikováno v:
Synthetic Communications. 2007, Vol. 37 Issue 7, p1053-1058. 6p. 2 Diagrams.
Publikováno v:
Synthetic Communications. 42:1824-1831
A novel and efficient one-pot preparation of 6-substituted pyrido-[2,3-d]pyrimidines by cyclocondensation of 6-amino-1,3-dimethyluracil with symmetrical vinamidinium salts under basic conditions has been developed. Regioselectivity was observed with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e43ed06765999f1a92e7836631d82232
https://doi.org/10.1080/00397911.2010.545163
https://doi.org/10.1080/00397911.2010.545163
Publikováno v:
Tetrahedron Letters. 52:764-766
Α series of substituted 3-acyl-6-aryl-2-pyridones have been prepared in one-step reactions via condensation of 3-aryl-3-chloropropeniminium salts with β-keto-amides. This efficient synthesis has the advantages of high yields and simple reaction pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0319624d32baa0c85fea83ed7a09a7e
https://doi.org/10.1016/j.tetlet.2010.12.012
https://doi.org/10.1016/j.tetlet.2010.12.012
Publikováno v:
ChemInform. 43
A novel and efficient one-pot preparation of 6-substituted pyrido-[2,3-d]pyrimidines by cyclocondensation of 6-amino-1,3-dimethyluracil with symmetrical vinamidinium salts under basic conditions has been developed. Regioselectivity was observed with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97d493f4f9ecfec9262ab811b073345f
https://doi.org/10.1002/chin.201238165
https://doi.org/10.1002/chin.201238165
Publikováno v:
ChemInform. 42
Α series of substituted 3-acyl-6-aryl-2-pyridones have been prepared in one-step reactions via condensation of 3-aryl-3-chloropropeniminium salts with β-keto-amides. This efficient synthesis has the advantages of high yields and simple reaction pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d74dc2710c8e4ca976a41330e827b93
https://doi.org/10.1002/chin.201121138
https://doi.org/10.1002/chin.201121138
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95de8cb9b6d3258d23144e04a79f99f3
https://doi.org/10.1002/chin.200741121
https://doi.org/10.1002/chin.200741121
Autor:
Jean-Pierre Genêt, Thouraya Gmiza, Ridha Touati, Séverine Jeulin, Virginie Ratovelomanana-Vidal, Béchir Ben Hassine, Coralie Deport
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2005,-, pp.2478-2482
SYNTHESIS, Georg Thieme Verlag, 2005,-, pp.2478-2482
Ru-SYNPHOS® and Ru-DIFLUORPHOS® catalysts were efficiently used for the synthesis of a wide variety of chiral p- hydroxy amides via asymmetric hydrogenation of the corresponding β-keto amides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a640e8d670314a3474fb1a9956bca6b4
https://hal.archives-ouvertes.fr/hal-00091891
https://hal.archives-ouvertes.fr/hal-00091891
Publikováno v:
ChemInform; Apr2008, Vol. 39 Issue 17, pno-no, 1p