Syntheses based on α-azidooximes: I. Reduction of α-azidooximes

Syntheses based on α-azidooximes: I. Reduction of α-azidooximes Full article

Journal

Russian Journal of Organic Chemistry
ISSN: 1608-3393 , E-ISSN: 1070-4280

Output data

Year: 2007, Volume: 43, Number: 8, Pages: 1106-1113 Pages count : 8 DOI: 10.1134/s1070428007080027

Authors

Sukhorukov A.Yu. ¹ , Semakin A.N. ¹ , Lesiv A.V. ¹ , Khomutova Yu.A. ¹ , Ioffe S.L. ¹

Affiliations

1	Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia

Convenient procedures were developed for selective and exhaustive reduction of α-azido-oximes that were easily prepared from aliphatic nitro compounds. Nitroalkanes were shown to be convenient precursors of β-functionalized amines (1,2-diamines, iminophosphonates, β azidohydroxyl-amines, α-aminooximes).

Sukhorukov A.Y. , Semakin A.N. , Lesiv A.V. , Khomutova Y.A. , Ioffe S.L.
Syntheses based on α-azidooximes: I. Reduction of α-azidooximes
Russian Journal of Organic Chemistry. 2007. V.43. N8. P.1106-1113. DOI: 10.1134/s1070428007080027 WOS Scopus OpenAlex

Web of science:	WOS:000249631300002
Scopus:	2-s2.0-34648840640
OpenAlex:	W2322897261

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