Anatoly T. Soldatenkov

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Continuing our work [1, 2] on synthesis and study of the dependences of the pesticidal activity on the structure of derivatives of [2,2]-para-cyclophane, we obtained a series of 1,2-disubstituted ethylenes which include a di(para-xylylene) moiety and aryl or pyridyl radicals. By condensation of 4-acetyl-[2,2]-para-cyclophane (I) with formylpyridines or(More)
In continued work [2] on the synthesis and study of the pesticidal activity of derivatives of piperidine we turned to the preparation of new substituted piperidine and tetrahydropyridines containing an aminoor an amido-group in position C(4). Condensation of benzaldehyde with acetoacetic ester in the presence of AcONH~ after treating the reaction mixture(More)
In continuation of our search for new biologically active compounds in the class of piperidine derivatives [1 – 5], we have synthesized a series of Nand O-acylated 2,6-diphenyl-4-hydroxypiperidines (I), 2,6-diphenyl-4-hydroxy1,2,3,6-tetrahydropyridines (II), and N-(phenylcarbamoyl)-piperidinone (III). The newly synthesized esters Ib and Id were obtained(More)
The title compound, C33H35N3O5, is the product of the multicomponent condensation of 1-benzyl-4-eth-oxy-carbonyl-piperidin-3-one with 1,5-bis-(2-formyl-phen-oxy)-3-oxapentane and ammonium acetate. The mol-ecule comprises a penta-cyclic system containing the aza-14-crown-4-ether macrocycle, tetra-hydro-pyrimidine, tetra-hydro-pyridine and two benzene rings.(More)
Data are given in this communication on the preparation of new substituted nitrophenylpyridines and their fungicidal activity and on the activity of some diand trialkylsubstituted nitrophenylpyridines synthesized by us previously [5]. This is a continuation of studies [2-4] on the synthesis and fungicidal properties of pyridine derivatives. The following(More)
With the goal of studying the structure and biological activity of new compounds of the [2,2]-para-cyclophane (PCP) series (I), based on its 4-acyl derivatives (II) we synthesized 4-hydroxymethyl-, 4-acyloxymethyl-, and 4-alkenyl-substituted para-cyclophanes (Ill-VII). The starting 4-acetylPCP (IIa) was obtained as in [4]. We synthesized 4-benozoylPCP (IIb)(More)
The title compound, C(23)H(23)NO, is the product of a tandem transformation of the double Mannich base bis-(1-oxo-1,2,3,4-tertrahydro-2-naphtho-ylmeth-yl)amine hydro-chloride in HBr solution upon heating. The tetra-hydro-pyridine ring has a non-symmetrical half-chair conformation, whereas the cyclo-hexa-diene and cyclo-hexene rings adopt non-symmetrical(More)
G. N. Pershin and N. S. Bogdanova, Chemotherapy of Viral Infections~ Moscow (1973). E. Dyer, R. E. Farries, Jr.~ C. E. Minner, et al., J. Org. Chem., 34, 973 (1969). T. P. Johnson, L. B. Holum, and J. A. Montgomery, J. Am. Chem. Soc., 80, 6265 (1958). J. H. Van Boom, L. Brandsma, and J. T. Arens, Rec. Tray. Chim. Pays-Bas, 87, 97 (1968). B. I. Ionin and A.(More)
The title compound, C40H41NO8, is a product of the reduction of the cyclic carbonyl group of the γ-piperidone subunit of the aza-14-crown-4 ether with subsequent re-esterification of its dimethyl butenoate substituent into a monoethyl monomethyl group. The aza-crown macrocycle exhibits a bowl conformation with a dihedral angle of 70.82 (5)° between the(More)