Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Martine Maillard-Boyer"'
Autor:
Martine Maillard-Boyer, Caroline Castera-Ducros, Pierre Verhaeghe, France Sifredi, Pascal Rathelot, Patrice Vanelle
Publikováno v:
Molecules, Vol 15, Iss 4, Pp 2719-2729 (2010)
A series of new quinazoline derivatives bearing a vinylic chloride group on the 2-position was prepared by using a consecutive SRN1 / ERC1 radical strategy.
Externí odkaz:
https://doaj.org/article/078b25b94c9f4c6db35fd97177b5681b
Autor:
Thierry Terme, Patrice Vanelle, Martine Maillard-Boyer, Marc Since, Omar Khoumeri, Pierre Verhaeghe
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2011, 52 (29), pp.3810--3813. 〈10.1016/j.tetlet.2011.05.060〉
Tetrahedron Letters, Elsevier, 2011, 52 (29), pp.3810--3813. ⟨10.1016/j.tetlet.2011.05.060⟩
Tetrahedron Letters, 2011, 52 (29), pp.3810--3813. ⟨10.1016/j.tetlet.2011.05.060⟩
Tetrahedron Letters, Elsevier, 2011, 52 (29), pp.3810--3813. 〈10.1016/j.tetlet.2011.05.060〉
Tetrahedron Letters, Elsevier, 2011, 52 (29), pp.3810--3813. ⟨10.1016/j.tetlet.2011.05.060⟩
Tetrahedron Letters, 2011, 52 (29), pp.3810--3813. ⟨10.1016/j.tetlet.2011.05.060⟩
International audience; We report herein the first example of a SNAr reaction using TDAE-initiated carbanions in quinazoline series. The o-nitrobenzyl carbanion, formed by the action of TDAE on o-nitrobenzyl chloride, reacts with 4-chloro-2-trihalome
Autor:
Omar Khoumeri, Pierre Verhaeghe, Martine Maillard-Boyer, Thierry Terme, Marc Since, Patrice Vanelle
Publikováno v:
ChemInform. 42
Treatment of o-nitrobenzyl chlorides with TDAE results in formation of carbanions which undergo SNAr reaction with 4-chloroquinazolines bearing trihalomethyl substituents to give the substituted derivatives (III).