Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marie Louise Dheu-Andries"'
Autor:
J. Lhomme, Nathalie Berthet, Marie Louise Dheu-Andries, Christian Coulombeau, Laurence Fouilloux, Julian Garcia, C. Coulombeau, Pierre Vatton
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 330:417-422
Molecular modeling of a DNA undecamer and a corresponding DNA apurinic undecamer (d(CGCACXCACGC) d(GCGTGTGTGCG), X = A or apurinic site) has been performed using the jumna program. Among the possible structures, several are slightly distorted and cor
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2009, 50 (50), pp.7038-7042. ⟨10.1016/j.tetlet.2009.09.175⟩
Tetrahedron Letters, Elsevier, 2009, 50 (50), pp.7038-7042. ⟨10.1016/j.tetlet.2009.09.175⟩
Carbohydrate-derived cyclic nitrones were deoxygenated to form the corresponding imines using tributylphosphine. Experimental and theoretical investigations by the way of MP2 calculations suggest a revision of the mechanism initially proposed by Kurt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a08be1cbc21716b1f86d2ad5b3e1ad49
https://hal.archives-ouvertes.fr/hal-01658997
https://hal.archives-ouvertes.fr/hal-01658997
Autor:
Martine Demeunynck, Marie-Paule Teulade-Fichou, Muriel Jourdan, David Monchaud, Pascal Dumy, Walid Zeghida, Marie-Louise Dheu-Andries, Julien Debray
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2009, 7 (24), pp.5219. ⟨10.1039/B912716J⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2009, 7 (24), ⟨10.1039/B912716J⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2009, 7 (24), pp.5219. ⟨10.1039/B912716J⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2009, 7 (24), ⟨10.1039/B912716J⟩
The present article reports on the design and the synthesis of a series of mono- and bis-pyrimidinoacridines and their evaluation as a novel family of quadruplex-binders. It is shown that bispyrimidinoacridines represent an interesting compromise bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d112f1b4b3b9f1f74156b5cd0fff52c0
https://hal.archives-ouvertes.fr/hal-02125664
https://hal.archives-ouvertes.fr/hal-02125664
Publikováno v:
Journal of Molecular Structure: THEOCHEM
Journal of Molecular Structure: THEOCHEM, Elsevier, 2007, 811, pp.175-182. ⟨10.1016/j.theochem.2007.03.009⟩
Journal of Molecular Structure: THEOCHEM, Elsevier, 2007, 811, pp.175-182
Journal of Molecular Structure: THEOCHEM, Elsevier, 2007, 811, pp.175-182. ⟨10.1016/j.theochem.2007.03.009⟩
Journal of Molecular Structure: THEOCHEM, Elsevier, 2007, 811, pp.175-182
International audience; We have performed a detailed study of the cyclization of carbonyl groups on unactivated alkynyl-quinolines. Two cyclization modes are accessible: the exo vs. endo mode. The influence of the substituents of the alkynyl-quinolin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4976a8759775e84acf4d5f3b1fb5fd89
https://hal.archives-ouvertes.fr/hal-00172453
https://hal.archives-ouvertes.fr/hal-00172453