182187-66-2Relevant academic research and scientific papers
Synthesis of α,ω-Bis-Enones by the Double Addition of Alkenyl Grignard Reagents to Diacid Weinreb Amides
Wiesler, Stefan,Bau, Michael A.,Niepel, Thomas,Younas, Sara L.,Luu, Hieu-Trinh,Streuff, Jan
, p. 6246 - 6260 (2019)
An efficient double addition of substituted alkenylmagnesium bromides to bis-Weinreb amides has been developed, giving α,ω-bis-enones that are building blocks for certain drugs and polymers. Furthermore, reliable protocols for the preparation of the requi
The total synthesis of favelanone
Ng, Wendy,Wege, Dieter
, p. 6797 - 6798 (1996)
(±)-Favelanone (1) has been synthesised by a sequence involving as the key step the cycloaddition of 6-methoxy-5-methyl-3-trimethylsilyloxyisobenzofuran-1-carbonitrile (3) to 7-bromo-5,5-dimethylbicyclo[4.1.0]hept-1(7)-ene (4).
