Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Jean-Jacques Youte"'
Autor:
Ho H. Lee, Sunali Mehta, H. D. Sarath Liyanage, Sally Y. Bai, Frederik B. Pruijn, Moana Tercel, Jean-Jacques Youte Tendoung
Publikováno v:
Journal of Medicinal Chemistry. 60:5834-5856
A new series of nitro analogues of the duocarmycins was prepared and evaluated for hypoxia-selective anticancer activity. The compounds incorporate 13 different amine-containing side chains designed to bind in the minor groove of DNA while spanning a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb0c1fc7d5d1e8990b20573f43bd7434
https://doi.org/10.1021/acs.jmedchem.7b00563
https://doi.org/10.1021/acs.jmedchem.7b00563
Autor:
Camille Jacquet, Stéphane P. Roche, Nagalakshmi Jeedimalla, Diana Bahneva, Jean-Jacques Youte Tendoung
Publikováno v:
The Journal of organic chemistry. 83(20)
A three-step sequence for the synthesis of α-arylated cyclohexanones and the most challenging cycloheptanones is reported. First, an efficient one-pot synthesis of β,β'-disubstituted benzylidene cycloalkanes (styrenes) using the palladium-catalyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd46394c5e8e69498feb073d77aa83d9
https://pubmed.ncbi.nlm.nih.gov/30089202
https://pubmed.ncbi.nlm.nih.gov/30089202
Publikováno v:
Tetrahedron. 71:3549-3591
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::443744468cbb21a647640a949e6ee160
https://doi.org/10.1016/j.tet.2014.06.054
https://doi.org/10.1016/j.tet.2014.06.054
Akademický článek
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Publikováno v:
Tetrahedron Letters. 52:7000-7003
The indoline scaffold of hypoxia selective prodrugs of DNA-alkylating agents related to the duocarmycin natural products was synthesized via an enantioselective Friedel–Crafts alkylation. Easily accessible starting materials and good stereoselectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d1dae00e4c18b013da9c56f771d7ad1
https://doi.org/10.1016/j.tetlet.2011.10.105
https://doi.org/10.1016/j.tetlet.2011.10.105
Autor:
K. Yoganathan, Nguyen Quang Vu, Tuan Minh Nguyen, Mark S. Butler, Jean-Jacques Youte, Ying San Ho, Jacelyn Lau, Christina L. L. Chai, Benjamin S.W. Tan, Angie Cheong
Publikováno v:
Tetrahedron. 66:9270-9276
The synthesis of the chiral core structure of the lissoclimide class of anti-tumour agents containing three rings, including a chiral succinimide subunit and an exocyclic double bond, has been investigated. The compound 7 was obtained, without the us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de8cedc5fb6cd8bd8bf8923032727171
https://doi.org/10.1016/j.tet.2010.09.031
https://doi.org/10.1016/j.tet.2010.09.031
Publikováno v:
ChemInform. 46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3947345fee615ab06d1830bfc713ae28
https://doi.org/10.1002/chin.201528289
https://doi.org/10.1002/chin.201528289
Akademický článek
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Autor:
Philippe Rasoanaivoa, Van Cuong Pham, François Frappier, Jean Jacques Youte, Roger Joyeau, François Trigalo
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2004, 60 (25), pp.5471-5474. ⟨10.1016/j.tet.2004.04.068⟩
Tetrahedron, Elsevier, 2004, 60 (25), pp.5471-5474. ⟨10.1016/j.tet.2004.04.068⟩
The syntheses of three malagashanine analogues are reported. They involve conversion of strychnobrasiline in multiple steps and obtaining (i) unsaturation of the bond 3-14, (ii) inversion of configuration on carbon C3, (iii) inversion of configuratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c95e5339f8146d11c3c545a28ca39d
https://doi.org/10.1016/j.tet.2004.04.068
https://doi.org/10.1016/j.tet.2004.04.068
Autor:
Jean-Jacques Youte, Roland Barret
Publikováno v:
Letters in Organic Chemistry. 5:537-539
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb956a00f47836515df3cf4f280208ae
https://doi.org/10.2174/157017808785982176
https://doi.org/10.2174/157017808785982176