ИСТИНА

Romanova IuM

Соавторы: Юровская М.А., Ямашкин С.А., Chernukha M., Khmel', Veselova M., Zaĭtseva I., Кокшарова О.А., Липасова В.А.

5 статей

Количество цитирований статей в журналах по данным Scopus: 13

IstinaResearcherID (IRID): 1220894

Деятельность

• Статьи в журналах

  • 
    • 2012 Mutants of Burkholderia cenocepacia with a change in synthesis of N-acyl-homoserine lactones--signal molecules of Quorum Sensing regulation
    • Veselova MA, Lipasova VA, Zaĭtseva IuV, Koksharova OA, Chernukha MIu, Romanova IuM, Khmel' IA
    • в журнале Russian Journal of Genetics, издательство Maik Nauka/Interperiodica Publishing (Russian Federation), том 48, № 5, с. 608-616
  • 
    • 2006 The potential use of 6-amino-5-methoxy(methyl)-2,3-dimethyl-and 6-amino-5-methoxy(methyl)-1,2,3-trimethyl-indoles in the synthesis of pyrrolo[2,3-f]quinolines
    • Yamashkin S.A.a, Oreshkina E.A.b, Romanova I.S.a, Yurovskaya M.A.c
    • в журнале Chemistry of Heterocyclic Compounds, издательство Kluwer Academic/Plenum Publishers (United States), том 42, № 1, с. 86-91 DOI
  • 
    • 2005 Synthesis of functionally substituted pyrrolo[3,2-g] quinolines from 6-amino-7-methoxy-1,2,3-trimethylindole
    • Yamashkin S.A.a, Oreshkina E.A.a, Romanova I.S.a, Yurovskaya M.A.b
    • в журнале Chemistry of Heterocyclic Compounds, издательство Kluwer Academic/Plenum Publishers (United States), том 41, № 10, с. 1280-1289 DOI
  • 
    • 2003 Synthesis of functionally substituted pyrrolo[2,3-g]- and pyrrolo[3,2-f]quinolines from 5-amino-2-phenyl- and 5-amino-1-methyl-2-phenylindoles
    • Yamashkin S.A.a, Romanova G.A.a, Romanova I.S.a, Yurovskaya M.A.b
    • в журнале Chemistry of Heterocyclic Compounds, издательство Kluwer Academic/Plenum Publishers (United States), том 39, № 9, с. 1188-1196 DOI
  • 
    • 2003 Synthesis of functionally substituted pyrrolo[3,2-h]quinolines from 2,3-dimethyl- and 1,2,3-trimethyl-7-aminoindoles
    • Yamashkin S.A.a, Romanova G.A.a, Romanova I.S.a, Yurovskaya M.A.b
    • в журнале Chemistry of Heterocyclic Compounds, издательство Kluwer Academic/Plenum Publishers (United States), том 39, № 8, с. 1048-1056 DOI