6630-86-0Relevant articles and documents
An efficient tandem oxidative-protection reaction of benzylic alcohols to corresponding arylhydrazones and oximes
Badri, Rashid,Shushizadeh, Mohammad Reza
, p. 601 - 605 (2007/10/03)
A mild and efficient one-pot synthesis of hydrazones and oximes from the reaction of the oxidation product of benzyl alcohols and phenols by 3,6-bis(triphenylphosphonium)cyclohexene dichromate with phenylhydrazine, 2,4-dinitrophenylhydrazine, and hydroxylamine is described. Copyright Taylor & Francis Group, LLC.
About the Photochromic and Thermochromic Effect of Benzil Phenylhydrazones
Mueller, U.,Timpe, H.-J.,Gustav, K.
, p. 876 - 892 (2007/10/02)
Benzil phenylhydrazone 1 synthesized from benzil and phenylhydrazine possesses s-trans-E configuration detected by means of quantum chemical calculations and its spectral data.Upon irradiation a photochromic process proceeds with λ-shift Δλ ca. 80nm.The p
Oxidation of Arylhydrazones by Thallium(III) Acetate - A Kinetic Analysis of Structural Effect on the Oxidation
Balakrishnan, R.,Srinivasan, V. S.,Venkatasubramanian, N.
, p. 476 - 478 (2007/10/02)
The kinetics of oxidation of the phenylhydrazones of several substituted benzaldehydes by Tl(III) has been studied in aqueous acetic acid in the presence of initially added sodium chloride (0.05M).The reaction exhibits a first order dependence on and and is retarded by added sodium chloride and sodium acetate.The reaction is accelerated by electron-releasing substituents in the benzaldehyde moiety while electron-withdrawing substituents retard the reaction.The reaction data obey Hammett relationship with ρ = -1.62.Electron-withdrawing groups in the phenylhydrazine moiety also reduce the reaction rate (ρ = -2.66).The major product of the reaction is the cis-monohydrazone of benzil.