1246887-64-8Relevant academic research and scientific papers
Asymmetric total synthesis of caribenol A via an intramolecular diels-alder reaction
Han, Jing-Chun,Liu, Lian-Zhu,Chang, Yuan-Yuan,Yue, Guo-Zong,Guo, Jie,Zhou, Li-Yan,Li, Chuang-Chuang,Yang, Zhen
, p. 5492 - 5504 (2013)
A total synthesis of the caribenol A (1), a novel natural product with an intriguing tetracyclic framework, has been achieved. The synthesis features an intramolecular Diels-Alder (IMDA) reaction for the facile construction of the tricyclic [5-7-6] skelet
Asymmetric total synthesis of caribenol A
Liu, Lian-Zhu,Han, Jin-Chun,Yue, Guo-Zong,Li, Chuang-Chuang,Yang, Zhen
, p. 13608 - 13609 (2010)
A unified strategy toward the asymmetric total synthesis of carbenol A is reported, featuring intramolecular Diels-Alder (IMDA) and biomimetic oxidation reactions as key steps.
