Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Barbara Monse"'
Autor:
Carol Joglar, Mario Roberto Quintanilla Gatica, Mariano Eliseo Rodríguez Malabrán, Bárbara Monserrat Soler Aqueveque
Publikováno v:
Edutec, Iss 83 (2023)
Alta percepción de autoeficacia (PAE) y sentir emociones positivas durante la búsqueda y gestión de la información en internet generan motivación en los estudiantes y son factores relevantes que inciden en su rendimiento académico. Por lo tanto
Externí odkaz:
https://doaj.org/article/d532b6d886054ba59a4d9059e272cc20
Publikováno v:
Tetrahedron. 51:1167-1176
Two pathways towards the construction of the trikentrin skeleton are presented, one leading to the total synthesis of (±)-cis-Trikentrin A (1). The key step is the intramolecular Heck coupling of the triflate 21 to form the five-membered ring of the
Publikováno v:
ChemInform. 26
Two pathways towards the construction of the trikentrin skeleton are presented, one leading to the total synthesis of (±)-cis-Trikentrin A (1). The key step is the intramolecular Heck coupling of the triflate 21 to form the five-membered ring of the
Autor:
Mike Hutton, Hanno Roder, Barbara Monse, Gabriele Hübinger, Cynthia Zehr, Jason L. Eriksen, Nikolaus Plesnila, Sylvie Le Corre, Mei Yue, Heidi Sahagún, Hans Klafki, Eileen McGowan, Jada Lewis, Dennis W. Dickson, Axel Obermeier, Pierfausto Seneci
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 103(25)
An orally bioavailable and blood–brain barrier penetrating analog of the kinase inhibitor K252a was able to prevent the typical motor deficits in the tau (P301L) transgenic mouse model (JNPL3) and markedly reduce soluble aggregated hyperphosphoryla
Autor:
Barbara Monse, Sylviane Thoret, Marie-Thérèse Martin, Daniel Guenard, Olivier Baudoin, Anne Decor, Angèle Chiaroni, Françoise Guéritte
Publikováno v:
Bioorganic and Medicinal Chemistry
Bioorganic and Medicinal Chemistry, Elsevier, 2006, 14(7), pp.2314-2332. ⟨10.1016/j.bmc.2005.11.011⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2006, 14, pp.2314-2332
Bioorganic and Medicinal Chemistry, Elsevier, 2006, 14(7), pp.2314-2332. ⟨10.1016/j.bmc.2005.11.011⟩
Bioorganic and Medicinal Chemistry, Elsevier, 2006, 14, pp.2314-2332
Three macrocyclic analogues of rhazinilam 1 having a 11- or 12-membered B-ring with an endocyclic carbamate group or an amino-acid residue were synthesized from the natural product. These analogues 3 and 4 displayed a very low activity on tubulin. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9920dba4628d6acbd18bd437cd67e81
https://hal.archives-ouvertes.fr/hal-00020659
https://hal.archives-ouvertes.fr/hal-00020659
Autor:
Laura Casiraghi, Barbara Monse, Wolfgang Froehner, Heidi Sahagún, Pierfausto Seneci, Tobias Braxmeier
Publikováno v:
Organic letters. 7(21)
[reactions: see text] Two complementary and efficient strategies have been developed for the regiospecific synthesis of unsymmetrical indolopyrrolocarbazoles (IPCs) mono-N-substituted with a pentacycle. A halogen in position 2 of the intermediate bis