13C NMR spectra of biologically active compounds

The diastereomeric effects on the¹³C NMR chemical shifts of thirteen epimeric pairs of 16-aryloxy-11-deoxyprostaglandins of the E₁ and F₁ series caused by the change in the configuration of the 15-hydroxy group, which are differential parameters for assigning epimers to the 15- and 15-stereochemical series, have been determined.For Communication (VIII), see [1].Institute of Chemistry, Bashkir Scientific Center, Urals Branch, Academy of Sciences of the USSR, Ufa. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 123–128, January–February, 1991.     

Pyrimidine derivatives. 58. A new method for synthesizing 7-aminopyrrolo[2,3-d]-pyrimidine derivatives

A number of aldimines of 7-aminopyrrolo[2,3-d]pyrimidine have been synthesized by the action of bromine on hydrazones of 5-allyl-4-hydrazinopyridine. The structures of the compounds obtained were confirmed by IR spectroscopy and mass spectrometry.For Communication 57, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 678–681, May, 1985.     

Analogs of pyrimidine mono- and polynucleotides

The corresponding monophosphates, cyclophosphates, and , -diphosphates were obtained by phosphorylation of 1-(1, 4-dihydroxy-2-pentyl) thymine, 1-(1, 3-dihydroxy-2-propyl) uracil, and their derivatives with selective protection of one of the hydroxyl groups. 2-Cyanoethyl phosphate (CEP) in the presence of N, N-dicyclohexylcarbodiimide (DCC), polyphosphoric acid, and pyrophosphoryl chloride were used as phosphorylating agents. The dependence of the yields of the products of phosphorylation of 1-(1, 4-dihydroxy-2-pentyl) thymine with CEP on the ratio of the reacting substances and the reaction time was studied. The monophosphates were cyclized under the influence of DCC. In the case of 1-(1, 3-dihydroxy-2-propyl) uracil 1-phosphate a dimeric phosphate was obtained in addition to a cyclophosphate. The acid hydrolysis of the cyclophosphates was investigated.See [1] for communication V; see [2] for a preliminary communication.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 678–683, May, 1978.     

Derivatives of l-H-aziridine-2-carboxylic acid

The reaction of 1,1-dimethylhydrazine with acrylic acid derivatives gave a number of 1,1-dimethyl-2-(2-substituted ethyl)hydrazines, which were quaternized by alkylating agents. The transformations of 1,1,1-trimethyl-2-(2-substituted ethyl)hydrazinium salts in the presence of sodium methoxide were investigated. 2-Cyano-, 2-carbomethoxy-, 2-carbethoxy-, and 2-carbodiethylamidoaziridines and a number of products of decomposition of the starting salts were obtained.