Zobrazeno 1 - 10
of 49
pro vyhledávání: '"N. N. Novitskaya"'
Autor:
G. P. Snigireva, V. A. Rumyantseva, E. I. Novikova, N. N. Novitskaya, E. N. Telysheva, E. D. Khazins, E. G. Shaikhaev
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 47, Iss 1, Pp 54-65 (2019)
Background: About 30% of cases of hereditary breast cancer (BC) are associated with the BRCA1 and BRCA2 gene mutations. The absence of the programs of mandatory genetic screening for hereditary BRCA-associated BC in Russia, as well as of an algorithm
Externí odkaz:
https://doaj.org/article/a77d95c4e6784a89abe00602f8beb251
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65293859a1359a67b806c66cfbb00d1e
https://doi.org/10.1002/chin.199547125
https://doi.org/10.1002/chin.199547125
Publikováno v:
ChemInform. 29
Oxidation of a mixture ofm- andp-(chloro-tert-butyl) cumenes (12:88) by molecular oxygen gives onlyp-(chloro-tert-butyl)cumene hydroperoxide in a high yield; this product can be used for the synthesis of the pyrethroid ethofenprox.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7741ad2e943f03030d6cf7b97894d802
https://doi.org/10.1002/chin.199837099
https://doi.org/10.1002/chin.199837099
Publikováno v:
Russian Chemical Bulletin. 47:1218-1220
Oxidation of a mixture ofm- andp-(chloro-tert-butyl) cumenes (12:88) by molecular oxygen gives onlyp-(chloro-tert-butyl)cumene hydroperoxide in a high yield; this product can be used for the synthesis of the pyrethroid ethofenprox.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d14b109b2318f29218a370175577c6ef
https://doi.org/10.1007/bf02503500
https://doi.org/10.1007/bf02503500
Publikováno v:
Pharmaceutical Chemistry Journal. 29:353-354
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fedb9ce6fd6618883fc3cfa818ae66a5
https://doi.org/10.1007/bf02219391
https://doi.org/10.1007/bf02219391
Autor:
R. V. Kunakova, G. K. Samirkhanova, A. M. Shakirova, Tolstikov Genrikh A, N. N. Novitskaya, K. N. Pervushina
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:313-317
A new method for the preparation of functional derivatives of sulfolane by ozonolysis of 13-thiabicyclo[8.2.1]-cis-5-tridecene and its derivatives was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62ae8b951bffe2eefdab94fdbefd640c
https://doi.org/10.1007/bf00472418
https://doi.org/10.1007/bf00472418
Publikováno v:
Chemistry of Heterocyclic Compounds. 13:843-847
The stereochemistry of the reactions of 4-hydroxy-2-sulfolene, 4-hydroxy-3-chlorosulfolane, and 3,4-epoxysulfolane with nucleophilic reagents was studied. The optimum conditions for the preparation of sulfolanes with oxygen-containing substituents we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ebc8fc0c48f75d74df31d39310ec146
https://doi.org/10.1007/bf00488905
https://doi.org/10.1007/bf00488905
Autor:
E. V. Dmitrieva, L. K. Yuldasheva, E. E. Zaev, R. V. Kunakova, Tolstikov Genrikh A, N. N. Novitskaya
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 25:365-369
Oxidation of 2,9-dichloro-13-thiabicyclo[8.2.1]cis-5-tridecene with tert-amyl hydroperoxide leads to the respective exo-sulfoxide and also to a derivative of 13-thiabicyclo[7.3.1]cis-5-tridecene, which is a product from rearrangement with enlargement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::786c19be91fc4588670c1199510615e0
https://doi.org/10.1007/bf00922476
https://doi.org/10.1007/bf00922476
Publikováno v:
Chemistry of Heterocyclic Compounds. 15:1309-1313
4-Hydroxy-2-sulfolene, 3-hydroxy-4-chlorosulfolane, and 3,4-epoxysulfolane react with thiols in alkaline media to give mixtures of cis,trans-3-hydroxy-4-alkylthisulfolanes in a ratio of 2∶3.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf4bab239e5765f5ff63bf48c75d074c
https://doi.org/10.1007/bf00514733
https://doi.org/10.1007/bf00514733
Autor:
Leonard M. Khalilov, R. G. Kantyukova, N. N. Novitskaya, G. A. Tolstlkov, L. K. Yuldasheva, Leonid V. Spirikhin, E. E. Zaev
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 26:359-362
1. The reaction of SCl2 with cyclohexene results in the formation of d,l-bis(2-chlorocyclohexyl)sulfide and meso-bis(2-chlorocyclohexyl) sulfide. Investigation of the PMR spectra of the deuterated compounds has established that the dichloro sulfides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8a8a5b64b4bfbd85ad1a6b30cbf342d
https://doi.org/10.1007/bf00921851
https://doi.org/10.1007/bf00921851