First example of autooxidation of methyl and cyclohexano groups attached to the pyrrole ring: stabilization effect of phenyldiazenyl substituents

Autor: Elena Yu. Schmidt, Elena Yu. Senotrusova, Igor A. Ushakov, Olga N. Kazheva, Oleg A. Dyachenko, Grigorii G. Alexandrov, Andrei V. Ivanova, Albina I. Mikhaleva, Boris A. Trofimov

Publikováno v: ARKIVOC, Vol 2010, Iss 2, Pp 352-359 (2010)

Externí odkaz: https://doaj.org/article/b80cae230977404b9aba657a3ae6c0a4

One-Pot Assembly of 7-Methylene-6,8-dioxabicyclo[3.2.1]octanes, Congeners of Frontalin, from Ketones and Acetylene

Autor: Olga N. Kazheva, Igor A. Ushakov, Elena V. Skital'tseva, Nadezhda I. Protsuk, Boris A. Trofimov, Elena Yu. Senotrusova, Grigorii G. Alexandrov, Oleg A. Dyachenko, Al'bina I. Mikhaleva, Elena Yu. Schmidt, Nadezhda V. Zorina

Publikováno v: European Journal of Organic Chemistry. 2009:5142-5145

A facile, consecutive, self-consisting assembly of two molecules of ketones with two molecules of acetylene to afford 7-methylene-6,8-dioxabicyclo[3.2.1]octanes, which are unknown congeners of widespread insect pheromones, has been discovered. The re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f0c4409c698582e40ed96e4b07192400
https://doi.org/10.1002/ejoc.200900853

New Hindered BODIPY Derivatives: Solution and Amorphous State Fluorescence Properties

Autor: Boris A. Trofimov, Rachel Méallet-Renault, Sophie Badré, Cécile Dumas-Verdes, Robert B. Pansu, Jean-Jacques Vachon, Pierre Audebert, Elena Yu. Schmidt, Elena Yu. Senotrusova, Carine Julien, Thanh Truc Vu, Gilles Clavier

Publikováno v: Journal of Physical Chemistry C
Journal of Physical Chemistry C, American Chemical Society, 2009, 113 (27), pp.11844-11855. ⟨10.1021/jp9019602⟩

International audience; Four new hindered boron-dipyrromethene (BODIPY) dyes have been engineered and synthesized by modification of the pyrrole substituents. The chromophores were designed to shift their absorption and emission wavelengths to the r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e72e2821928eba9e081030a9493254b
https://doi.org/10.1021/jp9019602

Synthesis of 1-vinylpyrrole-2-carbonitriles

Autor: Boris A. Trofimov, Elena V. Skital'tseva, Elena Yu. Schmidt, Andrey V. Ivanov, Al'bina I. Mikhaleva, Konstantin B. Petrushenko, Elena Yu. Senotrusova, Igor A. Ushakov, Alexander M. Vasil'tsov

Publikováno v: Tetrahedron Letters. 50:97-100

A new highly synthetically potent series of bifunctional pyrroles, 1-vinylpyrrole-2-carbonitriles, were synthesized from readily available 1-vinylpyrrole-2-carbaldehyde oximes by two methods: (1) reaction with acetylene (KOH/DMSO, 70 °C, 10 min, yie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9a749feffc59c5b4287739b8ade41227
https://doi.org/10.1016/j.tetlet.2008.10.104

2-Arylazo-1-vinylpyrroles: A Novel Promising Family of Reactive Dyes

Autor: Al'bina I. Mikhaleva, Konstantin B. Petrushenko, A. V. Afonin, Natalia S. Smolyanina, Elena Yu. Senotrusova, Alexander F. Schmidt, Alexander M. Vasil'tsov, Elena Yu. Schmidt, Igor A. Ushakov, Marina V. Markova, Alexey B. Zaitsev, V. V. Smirnov, Boris A. Trofimov, Olga N. Kazheva, Ludmila V. Morozova, Oleg A. Dyachenko

Publikováno v: European Journal of Organic Chemistry. 2006:4021-4033

New reactive dyes, 2-arylazo-1-vinylpyrroles, have been synthesized in 52–94 % yield by a modified azo coupling of readily accessible 1-vinylpyrroles with arenediazonium hydrocarbonates in aqueous ethanol (≈3:1) at 0 °C. The λmax values for the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::93fca656d11005d374bda25241c4ad71
https://doi.org/10.1002/ejoc.200600357