78657-67-7Relevant articles and documents
Gold-catalyzed allylation of aryl boronic acids: Accessing cross-coupling reactivity with gold
Levin, Mark D.,Toste, F. Dean
supporting information, p. 6211 - 6215 (2014/06/23)
A sp3-sp2 C?C cross-coupling reaction catalyzed by gold in the absence of a sacrificial oxidant is described. Vital to the success of this method is the implementation of a bimetallic catalyst bearing a bis(phosphino)amine ligand. A mechanistic hypothesis is presented, and observable transmetalation, C?Br oxidative addition, and C?C reductive elimination in a model gold complex are shown. We expect that this method will serve as a platform for the development of novel transformations involving redox-active gold catalysts.
Π-CYCLIZATION: THE SYNTHESIS OF (+/-)-SOLAVETIVONE AND (+/-)-HINESOL
Murai, Akio,Sato, Shingo,Masamune, Tadashi
, p. 1033 - 1036 (2007/10/02)
A general efficient approach leading to the total synthesis of (+/-)-solavetivone, (+/-)-hinesol, and related spirovetivanes, is described.The process involves stereoselective formation of the asymmetric center at C-7 by ?-cyclisation as a key step.