Zobrazeno 1 - 10
of 385
pro vyhledávání: '"Eduard B. Rusanov"'
Autor:
Georgyi Koidan, Nazar Tsyzoryk, Eduard B. Rusanov, Svitlana V. Shishkina, Mykhailo Vovk, Aleksandr Kostyuk
Publikováno v:
SynOpen, Vol 08, Iss 03, Pp 130-137 (2024)
Externí odkaz:
https://doaj.org/article/0094c90f0d194ccdbeb465fa0b9ab411
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 78, Iss 4, Pp 399-403 (2022)
The crystal structure of the title compound, [Ag2(VO2F2)2(C9H9N3)4], is presented. The molecular complex is based on the heterobimetallic AgI—VV fragment {AgI2(VVO2F2)2(tr)4} supported by four 1,2,4-triazole ligands [4-benzyl-(4H-1,2,4-triazol-4-yl
Externí odkaz:
https://doaj.org/article/f1f0e37052a14237ac8e0bf4406be443
Autor:
Alla I. Vaskevych, Nataliia O. Savinchuk, Ruslan I. Vaskevych, Eduard B. Rusanov, Oleksandr O. Grygorenko, Mykhailo V. Vovk
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 2787-2794 (2021)
A regioselective method for the synthesis of 1-(hydroxymethyl)-2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones – close structural analogs of naturally occurring vasicinone alkaloids – is described. The procedure is based on PIFA-initiated oxidativ
Externí odkaz:
https://doaj.org/article/3bba6cccc5804b5b96a1064aa52ae806
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 77, Iss 11, Pp 1103-1108 (2021)
The structure of the title salt, ammonium carbamoylcyanonitrosomethanide, NH4+·C3H2N3O2−, features the co-existence of different hydrogen-bonding patterns, which are specific to each of the three functional groups (nitroso, carbamoyl and cyano) of
Externí odkaz:
https://doaj.org/article/140ca9a30e37412c84616e04f5be0ff8
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 6, Pp 808-811 (2019)
The crystal structure of the title molecular complex, [Ag2{VO2F2}2(C13H17N3O2)4]·4H2O, supported by the heterofunctional ligand tr-ad-COOH [1-(1,2,4-triazol-4-yl)-3-carboxyadamantane] is reported. Four 1,2,4-triazole groups of the ligand link two Ag
Externí odkaz:
https://doaj.org/article/f769b4bd17eb4372877c61dd481fe8fa
Autor:
Svitlana O. Sotnik, Artem M. Mishchenko, Eduard B. Rusanov, Andriy V. Kozytskiy, Konstantin S. Gavrilenko, Sergey V. Ryabukhin, Dmitriy M. Volochnyuk, Sergey V. Kolotilov
Publikováno v:
Molecules, Vol 26, Iss 12, p 3507 (2021)
The third generation Buchwald precatalysts Pd(ABP)(Phos)(OMs) (also known as Phos Pd G3)) with XPhos and RuPhos were prepared in multigram scale by a modified procedure (ABP = fragment of C-deprotonated 2-aminobiphenyl, XPhos = 2-dicyclohexylphosphin
Externí odkaz:
https://doaj.org/article/4a2432fac6e947b3b25a75015a5e5e05
Publikováno v:
Current Chemistry Letters, Vol 6, Iss 2, Pp 49-54 (2017)
Readily available tetrachloro-2-aza-1,3-butadienes enter into directed cyclocondensation reaction with N-phenyl-1,2-cyclopentanediamine which leads to regioselective cyclopentane annulation by the 1,3,5-triazepine. The formation of the 1,3,5-triazepi
Externí odkaz:
https://doaj.org/article/d52ae5717f9b4ba2b543478e59392b6b
Autor:
Nikolay Yu. Gorobets, Valeriya P. Tkachova, Roman P. Tkachov, Oleksandr D. Dyachenko, Eduard B. Rusanov, Vladimir D. Dyachenko
Publikováno v:
ARKIVOC, Vol 2010, Iss 11, Pp 254-264 (2010)
Externí odkaz:
https://doaj.org/article/e73640ed610146d1b332e9d2ddcb5360
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 2, Pp m222-m223 (2011)
The title compound, [Ni(C7H6NO2)2], (I), is a second monoclinic polymorph of the compound, (II), reported by Srivastava et al. [Acta Cryst. (1967), 22, 922] and Mereiter [Private communication (2002) CCDC refcode NISALO01]. The bond lengths and angle
Externí odkaz:
https://doaj.org/article/5b15cd9d2487455aa1bceccc67e24a65
Publikováno v:
Acta Crystallographica Section C Structural Chemistry. 79:177-185
Developing the structures of organic materials that rely on the hydrogen bonding of multifunctional substrates is often complicated due to a competition between various possible motifs. In this context, the illustrative case of the carbamoylcyanonitr