1280608-67-4Relevant articles and documents
Total synthesis and absolute stereochemistry of seragakinone A
Takada, Akiomi,Hashimoto, Yoshimitsu,Takikawa, Hiroshi,Hikita, Katsuyoshi,Suzuki, Keisuke
, p. 2297 - 2301 (2011/04/16)
(Chemical Equation Presented) Cyclic transformation: The key transformations of the asymmetric total synthesis of the marine-derived natural product seragakinone A are two N-heterocyclic carbene catalyzed benzoin cyclizations that result in the construction of two rings and a pinacol-type rearrangement to install the angular prenyl substituent.