6871-57-4Relevant academic research and scientific papers
Asymmetric Total Syntheses of (?)-α-Lycorane, (?)-Zephyranthine, and Formal Synthesis of (+)-Clivonine
Chen, Yong-Jian,Cai, Sen-Lin,Wang, Chuan-Chuan,Cheng, Jin-Duo,Kramer, S?ren,Sun, Xing-Wen
, p. 1309 - 1313 (2017/06/23)
An asymmetric route to (?)-α-lycorane and (?)-zephyranthine, and a formal total synthesis of (+)-clivonine were achieved. A pivotal intermediate, which serves as a potent precursor for the divergent syntheses of these natural products, was accessed by a diastereoselective Pd-catalyzed cinnamylation of an N-tert-butanesulfinyl imine.
Catalytic asymmetric hydrogenation of α-arylcyclohexanones and total synthesis of (-)-α-lycorane
Li, Gang,Xie, Jian-Hua,Hou, Jing,Zhu, Shou-Fei,Zhou, Qi-Lin
, p. 1597 - 1604 (2013/07/05)
An efficient catalytic asymmetric hydrogenation of racemic α-arylcyclohexanones with an ethylene ketal group at the 5-position of the cyclohexane ring via dynamic kinetic resolution has been developed, giving chiral α-arylcyclohexanols with two contiguous
