Use of organomagnesium compounds for the synthesis of organic derivatives of group II–V elements in a nonethereal medium

Summary For the primary alkyl halides (R=from C₂H₅ to n-C₉H₁₉; halogen=C1, Br, and I) and the simplest aryl halides (R=C₆H₅ and p-CH₃C₆H₄) it was shown that the organomagnesium synthesis in absence of catalysts for the Grignard reaction can be applied with success to the preparation of heteroorganic compounds of elements of Groups II–IV (mercury, boron, aluminum, silicon, germanium, tin, phosphorus, arsenic, antimony).     

VI. Synthesis of Heterocyclic Analogs of γ-Aminobutyric Acid from 3,5-Dinitrobenzoic Acid

A series of 7-carboxy-3-R-1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes was synthesized by reduction of 3,5-dinitrobenzoic acid with sodium borohydride followed by Mannich reaction with formaldehyde and primary amines. The mechanism of decomposition under electron impact of the 3-azabicyclo[3.3.1]nonane was established. Enthalpies of formation of compounds synthesized were calculated by semiempirical PM3 method.     

Hydrogention and Oxidation of Allyl Alcohol in the Presence of Colloid Palladium In Situ

Kinetic regularities of hydrogenation, oxidation with oxygen, and condensation of allyl alcohol in the presence of colloid palladium in situ were revealed. A mechanism of the reactions was proposed.     

Acylation and Sulfonation of the Enol Form of Phosphorylated Aldehydes

Russian Journal of General Chemistry -     

Synthesis of carbamoylformhydroxymoyl chlorides and study of their reactivities

Carbamoylformhydroxymoyl chlorides were synthesized by the reactions of carbamoylformamide oximes with sodium nitrite in the presence of hydrochloric acid, and their reactivities were examined.     

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.