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pro vyhledávání: '"Sergey V. Dragan"'
Autor:
Alexey S. Sazhnev, Sergey V. Dragan
Publikováno v:
Acta Biologica Sibirica, Vol 6, Iss , Pp 399-406 (2020)
The recent status of the family Heteroceridae in Siberia is discussed and the main references are given. From ten species of the Heteroceridae, which have been reported for the fauna of Siberia, only one species Heterocerus parallelus Gebler, 1830 wa
Externí odkaz:
https://doaj.org/article/d854ad460c7646cc8e7b2ac32d0052ef
Autor:
Sergey V. Dragan
Publikováno v:
Samara Journal of Science. 9:54-57
For a little more than a century, researchers have been studying the fauna of caddisflies of streams and lakes of the Ergaki Natural Park. The paper provides a brief overview of studies of the caddisfly fauna in the upper part of the Oya and Us river
Autor:
Sergey V. Dragan, Alexey S. Sazhnev
Publikováno v:
Acta Biologica Sibirica, Vol 6, Iss, Pp 399-406 (2020)
Acta Biologica Sibirica 6: 399-406
Acta Biologica Sibirica 6: 399-406
The recent status of the family Heteroceridae in Siberia is discussed and the main references are given. From ten species of the Heteroceridae, which have been reported for the fauna of Siberia, only one species Heterocerus parallelus Gebler, 1830 wa
Publikováno v:
Natural Product Communications. 14:1934578X1986068
Reinvestigation of 2-hydroxy-3-alkylnaphthoquinones oxidative dimerization was carried out. On the example of dihydrolapachol it is shown that the oxidative dimerization of 2-hydroxy-3-alkylnaphthoquinones upon treatment with lead tetraacetate or cer
Autor:
V. Ph. Anufriev, Dmitry N. Pelageev, Vladimir A. Denisenko, D. V. Berdishev, M. A. Pushilin, V. P. Glasunov, Sergey V. Dragan
Publikováno v:
Russian Chemical Bulletin. 61:2102-2108
The resulting products of oxidative coupling of substituted 3-alkyl-2-hydroxynaphthazarins in the presence of lead dioxide are the compounds with 7,14-dibenzo[a,i]oxanthrene skeleton.
Publikováno v:
Tetrahedron Letters. 52:3651-3653
A reinvestigation of cuculoquinone, previously isolated from the lichen Cetraria cucullata , led to a revision of the proposed structure to 3,3′-bis(6-ethyl-2,5,7,8-tetrahydroxy-1,4-naphthoquinone). The new structure was confirmed by synthesis.