Influence of the Chemical Structure of 4-Hydroxybenzylidenealkanones on Nonlinear Optical Properties of Their Complexes with Poly-1,10-Decamethyleneacetamidine

The influence exerted by the length exerted by the conjugation chain in 4-hydroxybenzylidenealkanones on the generation of the third harmonic by complexes of these chromophores with aliphatic polyamidine was studied.     

A new method for the generation of stable phenoxyl radicals by the reaction of [(Me3Si)2N]2E (E = Ge,Sn) with sterically hindered phenols

An unusual reaction of diaminogermylene and diaminostannylene with sterically hindered phenols which leads to the formation of stable phenoxyl radicals in high concentrations was found. The reaction mechanism was proposed. Amides [(Me₃Si)₂N]₂E (E = Ge, Sn) were investigated electrochemically.     

Reaction of 2-chloro-5-methylbenzoquinone with Β-aminocrotonic ester derivatives

The reaction of 2-chloro-5-methylbenzoquinone with -aminocrotonic ester derivatives was studied by PMR spectroscopy in CD₃COOD. The spectra indicate the formation of intermediate hydroquinone and quinone derivatives, which subsequently transform into the corresponding indoles. It was shown that the indolization proceeds unequivocally at the 3-position of the initial benzoquinone, and the rate of formation of the indole derivatives decreases with increase in the size of the substituent at the nitrogen atom of the -aminocrotonic ester. The starting, intermediate compounds and the end products observed in the PMR spectra were identified by comparison with specially synthesized compounds.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 324–328, March, 1990.     

Reaction of 2,3-epoxypropyl alkyl sulfides with carboxylic acids and phenol

Russian Chemical Bulletin -     

Phenyl Migration into the β Position of an α-Acetylenic Group in a Pentavalent Phosphorus Compound

Russian Journal of General Chemistry -