1202448-27-8Relevant articles and documents
Enantioselective synthesis of functionalized fluorinated cyclohexenones via Robinson annulation catalyzed by primary-secondary diamines
Cui, Hai-Feng,Yang, Ying-Quan,Chai, Zhuo,Li, Peng,Zheng, Chang-Wu,Zhu, Shi-Zheng,Zhao, Gang
supporting information; experimental part, p. 117 - 122 (2010/04/04)
(Chemical Presented) Primary-secondary diamine catalysts were used to catalyze the asymmetric Robinson annulation to synthesize multiply substituted fluorinated chiral cyclohexenones with two contiguous stereogenic centers, one of which is a fluorinated quaternary chiral center, with excellent enantioselectivities and diastereoselectivities in moderate to good yields.