Polyalkoxy-substituted nitrostilbenes in the synthesis of lamellarin analogs. Formal synthesis of lamellarin H

Polyalkoxy-substituted nitrostilbenes in the synthesis of lamellarin analogs. Formal synthesis of lamellarin H Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2023, Volume: 72, Number: 9, Pages: 2090-2094 Pages count : 5 DOI: 10.1007/s11172-023-4003-y

Authors

Silyanova E.A. ¹ , Maksimenko A.S. ¹ , Brunner M.D. ¹ , Koblov I.A. ¹ , Kislyi V.P. ¹ , Samet A.V. ¹ , Semenov V.V. ¹

Affiliations

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

Lamellarin D trimethyl ether was prepared by 1,3-dipolar cycloaddition of 6,7-dimethoxyisoquinolinium ylide to pentamethoxy-substituted nitrostilbene followed by a lactone ring closure in the intermediate cycloadduct. This approach allowed a formal synthesis of lamellarin H.

Silyanova E.A. , Maksimenko A.S. , Brunner M.D. , Koblov I.A. , Kislyi V.P. , Samet A.V. , Semenov V.V.
Polyalkoxy-substituted nitrostilbenes in the synthesis of lamellarin analogs. Formal synthesis of lamellarin H
Russian Chemical Bulletin. 2023. V.72. N9. P.2090-2094. DOI: 10.1007/s11172-023-4003-y WOS Scopus OpenAlex

Web of science:	WOS:001074328300014
Scopus:	2-s2.0-85172144715
OpenAlex:	W4387053675

DB	Citing
OpenAlex	6
Scopus	5
Web of science	6