124268-74-2Relevant academic research and scientific papers
Asymmetric, stereocontrolled total synthesis of (-)-brevianamide B
Williams, Robert M.,Glinka, Tomasz,Kwast, Ewa,Coffman, Hazel,Stille, James K.
, p. 808 - 821 (2007/10/02)
The asymmetric, stereocontrolled total synthesis of (-)-brevianamide B (2) is described. The synthesis features a stereocontrolled intramolecular SN2′ cyclization to construct the central bicyclo[2.2.2] nucleus. A synthetic route to C-10-epibre
PROMISING CYCLIZATION REACTIONS TO CONSTRUCT THE RING SYSTEMS OF BREVIANAMIDES A,B
Williams, Robert M.,Glinka, Tomasz
, p. 3581 - 3584 (2007/10/02)
An effective intramolecular Michael cyclization and intramolecular SN2'cyclization is described for constructing the tricyclic framework of the natural mycotoxins brevianamides A,B.
