101028-21-1Relevant articles and documents
A new method for the synthesis of Z-enediones via IBX-mediated oxidative rearrangement of 2-alkynyl alcohol systems
Crone, Benedikt,Kirsch, Stefan F.
, p. 764 - 766 (2008/02/03)
o-Iodoxybenzoic acid (IBX) was found to mediate the conversion of α-alkynyl alcohols into Z-enediones under notably mild conditions via a novel rearrangement mechanism (33-65% yield, 13 examples). The Royal Society of Chemistry 2006.
Selective oxyfunctionalization of (tricarbonylcyclohexadiene)iron-substituted furans with singlet oxygen and dimethyldioxirane
Adam, Waldemar,Schuhmann, Rosemarie M.
, p. 635 - 640 (2007/10/03)
The versatility of the tricarbonyliron fragment as protecting group in the oxyfunctionalization of cyclohexadienyl-substituted furans with singlet oxygen (1O2), dimethyldioxirane (DMD) and m-chloroperoxybenzoic acid (mCPBA) was inves