Pseudonitrosites as masked nitroalkenes in the Barton–Zard pyrrole synthesis

Pseudonitrosites as masked nitroalkenes in the Barton–Zard pyrrole synthesis Full article

Journal

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

Output data

Year: 2020, Volume: 30, Number: 4, Pages: 485-486 Pages count : 2 DOI: 10.1016/j.mencom.2020.07.026

Authors

Rusanov Daniil A. ^1,2 , Myshlyavtsev Andrey B. ^1,2 , Silyanova Eugenia A. ² , Samet Alexander V. ² , Semenov Victor V. ²

Affiliations

1	D. I. Mendeleev University of Chemical Technology of Russia, 125047 Moscow, Russian Federation
2	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

3-Aryl-4-methylpyrrole-2-carboxylates were prepared via the Barton–Zard reaction using pseudonitrosites as a source of the corresponding nitroalkenes. The starting pseudonitrosites were, in turn, obtained via addition of N2O3 to propenylbenzenes available from the natural plant essential oils.

Rusanov D.A. , Myshlyavtsev A.B. , Silyanova E.A. , Samet A.V. , Semenov V.V.
Pseudonitrosites as masked nitroalkenes in the Barton–Zard pyrrole synthesis
Mendeleev Communications. 2020. V.30. N4. P.485-486. DOI: 10.1016/j.mencom.2020.07.026 WOS Scopus OpenAlex

Web of science:	WOS:000557884000026
Scopus:	2-s2.0-85088986500
OpenAlex:	W3047083721

DB	Citing
OpenAlex	3
Scopus	3
Web of science	3