Reactions of silyl nitronates with dimethylformamide dimethyl acetal as a new general procedure for the synthesis of 2-nitroenamines

Reactions of silyl nitronates with dimethylformamide dimethyl acetal as a new general procedure for the synthesis of 2-nitroenamines Full article

Journal

Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581

Output data

Year: 2014, Volume: 55, Number: 45, Pages: 6220-6223 Pages count : 4 DOI: 10.1016/j.tetlet.2014.09.071

Authors

Shved Alexander S. ^1,2 , Tabolin Andrey A. ² , Khomutova Yulia A. ² , Ioffe Sema L. ²

Affiliations

1	Higher Chemical College of the Russian Academy of Sciences, D. I. Mendeleev University of Chemical Technology of Russia, Miusskaya sq. 9, Moscow 125047, Russian Federation
2	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prosp. 47, Moscow 119991, Russian Federation

Silyl nitronates obtained in situ from the corresponding aliphatic nitro compounds react with dimethylformamide dimethyl acetal giving 2-nitroenamines in moderate to good yields. The reaction pathway is discussed.

Shved A.S. , Tabolin A.A. , Khomutova Y.A. , Ioffe S.L.
Reactions of silyl nitronates with dimethylformamide dimethyl acetal as a new general procedure for the synthesis of 2-nitroenamines
Tetrahedron Letters. 2014. V.55. N45. P.6220-6223. DOI: 10.1016/j.tetlet.2014.09.071 WOS Scopus OpenAlex

≡ Web of science:	WOS:000344204600016
≡ Scopus:	2-s2.0-84908269348
≡ OpenAlex:	W2949452219