The preparation and resolution of 2-(2-pyridyl)-and 2-(2-pyrazinyl)-Quinazolinap and their application in palladium-catalysed allylic substitution
SP Flanagan, R Goddard, PJ Guiry
Index: Flanagan, Susan P.; Goddard, Richard; Guiry, Patrick J. Tetrahedron, 2005 , vol. 61, # 41 p. 9808 - 9821
Full Text: HTML
Citation Number: 40
Abstract
The preparation and resolution of two new axially chiral quinazoline-containing phosphinamine ligands, 2-(2-pyridyl)-Quinazolinap and 2-(2-pyrazinyl)-Quinazolinap, is described. The ligands were synthesised in good yield over eight steps and included two Pd- catalysed reactions, a Suzuki coupling to form the biaryl linkage and the introduction of the diphenylphosphino group, as the key transformations. The racemic ligands were resolved ...
Related Articles:
Light induced oxidation of 2, 3-dihydroquinazolin-4 (1H)-ones
[Memarian, Hamid R.; Ebrahimi, Saeid Journal of Photochemistry and Photobiology A: Chemistry, 2013 , vol. 271, p. 8 - 15]
[Linschoten; Gaisser; Van Der Goot; Timmerman European Journal of Medicinal Chemistry, 1984 , vol. 19, # 2 p. 137 - 142]
[Linschoten; Gaisser; Van Der Goot; Timmerman European Journal of Medicinal Chemistry, 1984 , vol. 19, # 2 p. 137 - 142]
[Linschoten; Gaisser; Van Der Goot; Timmerman European Journal of Medicinal Chemistry, 1984 , vol. 19, # 2 p. 137 - 142]