1,3-Dipolar Cycloaddition of a Nitronyl Nitroxide-Substituted Alkyne to Heteroaromatic N-Imines

1,3-Dipolar Cycloaddition of a Nitronyl Nitroxide-Substituted Alkyne to Heteroaromatic N-Imines Full article

Journal

Australian Journal of Chemistry
ISSN: 0004-9425 , E-ISSN: 1445-0038

Output data

Year: 2017, Volume: 70, Number: 12, Pages: 1317-1320 Pages count : DOI: 10.1071/CH17476

Authors

Romanov Vasiliy ^1,2 , Vorob'ev Aleksey ^1,2 , Bagryanskaya Irina ^1,2 , Parkhomenko Dmitriy ¹ , Tretyakov Evgeny ^1,2

Affiliations

1	(Данные Web of science) NN Vorozhtsov Inst Organ Chem, 9 Ac Lavrentiev Ave, Novosibirsk 630090, Russia
2	(Данные Web of science) Novosibirsk State Univ, Natl Res Univ, 2 Pirogova St, Novosibirsk 630090, Russia

1,3-Dipolar cycloaddition of the triple bond in an ethynyl-substituted nitronyl nitroxide to heteroaromatic N-imines is described. The reaction opens a pathway to polyfunctional nitronyl nitroxides with pyrazolo[1,5-a]pyridine or related substituents. According to X-ray diffraction analysis, dihedral angles between the plane of the paramagnetic moiety and heteroaromatic cycle do not exceed 24 degrees. Reactions between Cu(hfac)(2) (hfac = hexafluoroacetylacetonate ion) and a pyrazolo[1,5-a] pyridine-substituted radical produced a polymer chain complex with a 'head-to-tail' motif resembling that in breathing crystals.

Romanov V. , Vorob'ev A. , Bagryanskaya I. , Parkhomenko D. , Tretyakov E.
1,3-Dipolar Cycloaddition of a Nitronyl Nitroxide-Substituted Alkyne to Heteroaromatic N-Imines
Australian Journal of Chemistry. 2017. V.70. N12. P.1317-1320. DOI: 10.1071/CH17476 WOS Scopus РИНЦ OpenAlex

Web of science:	WOS:000415726600011
Scopus:	2-s2.0-85034788365
Elibrary:	31051538
OpenAlex:	W2755612228

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Web of science	3
Scopus	4
Elibrary	4
OpenAlex	3