19176-78-4Relevant academic research and scientific papers
Copper-catalyzed coupling reaction of c-ome bonds adjacent to a nitrogen atom with terminal alkynes
Yao, Bangben,Zhang, Yuhong,Li, Yong
supporting information; experimental part, p. 4554 - 4561 (2010/09/10)
(Figure presented) The cross coupling of the C-OMe bond adjacent to a nitrogen atom in dialkoxy-N,N-dialkylmethanamines with terminal alkynes was efficiently approached in the presence of copper catalyst under mild conditions to give 3-amino-1,4-diynes in good yields. The reaction is promoted by phosphine ligands and the chemistry provides a simple and efficient route to 3-amino-1,4-diynes. Importantly, the Michael addition occurred with as-prepared 3-amino-1,4-diynes to give the useful Michael-adducts containing tert-alkylamines in a very convenient way. Further studies revealed that (E)-1,5-diarylpent-1-en-4-yn-3-one was formed through the rearrangement by using the neutral alumina column, and the corresponding imine 2-(1,5-diphenylpent-2- en-4-ynylideneamino)ethanol was obtained in the presence of AgOTf.
Synthese regiospecifique d'amines tertiaires a groupe secondaire bi-insature
Mesnard, D.,Miginiac, L.
, p. 1 - 10 (2007/10/02)
We describe the regiospecific preparation of tertiary amines with a symmetrical (or dissymetrical) doubly unsaturated secondary group, by reaction of an allylic, vinylic or acetylenic organometallic derivative with a dialkylformamido acetal, a chlorinated iminium salt or an alkynyl aminoether.
