153864-61-0Relevant articles and documents
Oxidation of hydrazones by hypervalent organoiodine reagents: Regeneration of the carbonyl group and facile syntheses of α-acetoxy and α-alkoxy azo compounds
Barton, Derek H. R.,Jaszberenyi, Joseph Cs.,Liu, Wansheng,Shinada, Tetsuro
, p. 14673 - 14688 (2007/10/03)
Various hydrazone derivatives of α-keto esters were prepared. The carbonyl group was readily regenerated in high yield from phenylhydrazones through oxidative hydrolysis using hypervalent organoiodine(III) reagents either bis(trifluoroacetoxy)-iodobenzene (BTIB) in aqueous acetonitrile or hydroxy(tosyloxy)iodobenzene (HTIB) in chloroform. α-Acotxy phenyl- or methylazo compounds were readily synthesized by oxidation of the corresponding hydrazones with iodobenzene diacetate (IBDA) in dichloromethane or acetic acid. α-Methoxy phenyl- or methylazo compounds were also prepared by oxidation of the hydrazones in methanol. The mechanisms of the oxidation reactions are discussed.
Oxidation of phenylhydrazones of α-keto esters with hypervalent organoiodine reagents
Barton, Derek H. R.,Jaszberenyi, Joseph Cs.,Shinada, Tetsuro
, p. 7191 - 7194 (2007/10/02)
α-Ketoacids and ketones can easily be regenerated in high yield from their phenylhydrazones via hydroxy azo compounds upon oxidation with hupervalent iodine reagents.
