Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dilyara Chulakova"'
Autor:
Olga A. Lodochnikova, K. Tanaka, Dilyara Chulakova, Igor A. Litvinov, D. P. Gerasimova, Almira Kurbangalieva, A. R. Pradipta
Publikováno v:
Journal of Structural Chemistry. 61:119-125
The work juxtaposes crystal structures of two hydrochlorides of eight-membered 1,5-diazaheterocycles with chiral aminoindanole fragments located at the nitrogen atoms and having similar configurations. In spite of chemical and stereochemical identity
Autor:
Katsunori Tanaka, Ivan S. Smirnov, Kseniya S. Bulygina, Konstantin S. Usachev, Almira Kurbangalieva, Dilyara Chulakova, L. Z. Latypova, Ambara R. Pradipta, Danil R. Kuznetsov, Olga A. Lodochnikova
Publikováno v:
Chemistry – An Asian Journal. 14:4048-4054
The chiral substituted 1,5-diazacyclooctane (1,5-DACO) is of considerable importance and has attracted attention from a wide range of fields due to their unique chemical and biological properties. Despite the application potential, further study has
Autor:
Almira Kurbangalieva, Katsunori Tanaka, Ayumi Tsutsui, Dilyara Chulakova, L. Z. Latypova, Ivan V. Smirnov, Ambara R. Pradipta
Publikováno v:
BioNanoScience. 6(No. 4):364-367
Despite being fundamentally ubiquitous and important species in organic and bioorganic chemistry, the reactivities of N-alkyl-α,β-unsaturated imines have not been thoroughly explored due to their instability. Here, we describe novel reactivities of
Autor:
Almira Kurbangalieva, G. A. Chmutova, Dilyara Chulakova, Olga A. Lodochnikova, E. A. Berdnikov, L. Z. Latypova, E. Sh. Saigitbatalova
Publikováno v:
Russian Journal of Organic Chemistry. 50:521-534
A number of 4- and 5-R-sulfanylfuran-2(5H)-one derivatives were synthesized, and their oxidation with various reagents was studied. The corresponding sulfones were obtained using hydrogen peroxide in acetic acid. 4-R-sulfanyl derivatives were selecti
Autor:
Katsunori Tanaka, Dilyara Chulakova, L. Z. Latypova, Ambara R. Pradipta, Almira Kurbangalieva, Ivan V. Smirnov
Publikováno v:
HETEROCYCLES. 97:668