Intramolecular 1,3-Dipolar Cycloaddition of Alkenylnitrones of the 4H-Imidazole Series: Synthesis of a New Nitroxide pH-Sensitive Spin Probe

Intramolecular 1,3-Dipolar Cycloaddition of Alkenylnitrones of the 4H-Imidazole Series: Synthesis of a New Nitroxide pH-Sensitive Spin Probe Научная публикация

Журнал

Synthesis
ISSN: 0039-7881

Вых. Данные

Год: 2010, Номер: 2, Страницы: 343-348 Страниц : DOI: 10.1055/s-0029-1217109

Ключевые слова

1,3-dipolar cycloaddition; low-valence titanium; nitroxide radical; 4H-imidazole 3-oxide; pH-sensitive spin probe

Авторы

Morozov Denis A. ^1,2 , Kirilyuk Igor A. ¹ , Gatilov Yuri V. ¹ , Bagryanskaya Irina Yu. ¹ , Bozhko Julya Yu. ³ , Komarov Denis A. ³ , Grigor'ev Igor A. ¹

Организации

1	(Данные Web of science) Novosibirsk Inst Organ Chem SB RAS, Novosibirsk 630090, Russia
2	(Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
3	(Данные Web of science) Inst Chem Kinet & Combust SB RAS, Novosibirsk 630090, Russia

A new method was used for the preparation of a pH-sensitive spin probe involving an intramolecular 1,3-dipolar cycloaddition - reductive isoxazolidine ring-opening - oxidation reaction sequence. 2-(2-Allyloxyphenyl)-5-R-4,4-dimethyl-4H-imidazole-3-oxides (R = Me, NMe2), prepared from 3-hydroxylamino-3-methylbutan-2-one, undergo intramolecular 1,3-dipolar cycloaddition upon heating in toluene. Treatment of the cycloadducts with low-valence titanium (LVT) reagent resulted in reductive cleavage of the N-O bond of the isoxazolidine ring to give 3'-hydroxymethyl-5,5-dimethyl-4-R-2,5-dihydrospiro[imidazol-2,4'-chromane]s. The amine ( R = NMe2) was then oxidized with MCPBA to the target nitroxide 3'-hydroxymethyl-5,5-dimethyl-4-dimethylamino-2,5-dihydrospiro[imidazole-2,4'-chroman]-1-oxyl.

Morozov D.A. , Kirilyuk I.A. , Gatilov Y.V. , Bagryanskaya I.Y. , Bozhko J.Y. , Komarov D.A. , Grigor'ev I.A.
Intramolecular 1,3-Dipolar Cycloaddition of Alkenylnitrones of the 4H-Imidazole Series: Synthesis of a New Nitroxide pH-Sensitive Spin Probe
Synthesis. 2010. N2. P.343-348. DOI: 10.1055/s-0029-1217109 WOS Scopus РИНЦ OpenAlex

Опубликована online:	6 нояб. 2009 г.
Опубликована в печати:	1 янв. 2010 г.

Web of science:	WOS:000274245900021
Scopus:	2-s2.0-73949133013
РИНЦ:	15316930
OpenAlex:	W2061477056

БД	Цитирований
Web of science	1
Scopus	8
РИНЦ	6
OpenAlex	8