Stereoselective synthesis of spirocyclic nitronates by SnCl4-promoted reaction of nitroalkenes with C-2 substituted 4-methylidene-1,3-dioxolane

Stereoselective synthesis of spirocyclic nitronates by SnCl4-promoted reaction of nitroalkenes with C-2 substituted 4-methylidene-1,3-dioxolane Full article

Journal

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Output data

Year: 2015, Volume: 25, Number: 6, Pages: 449-451 Pages count : 3 DOI: 10.1016/j.mencom.2015.11.017

Authors

Mikhaylov Andrey A. ¹ , Zhmurov Petr A. ¹ , Naumova Anastasia S. ¹ , Khoroshutina Yulia A. ¹ , Sukhorukov Alexey Yu. ¹ , Ioffe Sema L. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

SnCl4-promoted [4 + 2] cycloaddition of β-nitrostyrenes to 4-methylidene-1,3-dioxolane provides stereoselective synthesis of spirocyclic nitronates. 2-Nitrovinyl benzoate under the same conditions produces δ-substituted nitrodiene as a single E,E-isomer.

Mikhaylov A.A. , Zhmurov P.A. , Naumova A.S. , Khoroshutina Y.A. , Sukhorukov A.Y. , Ioffe S.L.
Stereoselective synthesis of spirocyclic nitronates by SnCl4-promoted reaction of nitroalkenes with C-2 substituted 4-methylidene-1,3-dioxolane
Mendeleev Communications. 2015. V.25. N6. P.449-451. DOI: 10.1016/j.mencom.2015.11.017 WOS Scopus OpenAlex

Web of science:	WOS:000367761800017
Scopus:	2-s2.0-84951289893
OpenAlex:	W2218329380

DB	Citing
OpenAlex	8
Scopus	9
Web of science	8