107535-11-5Relevant academic research and scientific papers
A novel boron trifluoride etherate mediated deep-seated rearrangement of an α,β-epoxyketone
Srikrishna, Adusumilli,Ramasastry, Sripada S. V.
, p. 2973 - 2979 (2007/10/03)
Acid catalysed reaction of carvone epoxide 2 resulted in dimeric products 3 and 4, in contrast to the expected ring contraction product. Reaction of β-methylcarvone epoxides 8 and 11 with acids furnished 2-acetyl-4- isopropenylcyclopentanones 9 and 14 containing a stereodefined quaternary carbon atom. On the other hand, the reaction of epoxides 8 and 11 with boron trifluoride etherate lacks the stereoselectivity and in addition, anti-epoxide 8 furnished lactone 18 via an unusual deep seated rearrangement.
The Synthesis of 3,10-Dihydroxydielmentha-5,11-diene-4,9-dione
Carman, Raymond M.,Owsia, Soraya,Dongen, Jacobus M. A. M. Van
, p. 333 - 340 (2007/10/02)
A synthesis is reported for the title compound.
The Indans Formed by Dimerization of some Aromatic Terpenoids
Carman, Raymond M.,Dongen Jacobus M. A. M. Van
, p. 817 - 820 (2007/10/02)
Previous upon the dimerization of carvacrol derivatives to form indans is corrected.
