Different Behavior of 2-Substituted 3-Nitro-2<i>H</i>-chromenes in the Reaction with Stabilized Azomethine Ylides Generated from α-Iminoesters

Different Behavior of 2-Substituted 3-Nitro-2<i>H</i>-chromenes in the Reaction with Stabilized Azomethine Ylides Generated from α-Iminoesters

The AgOAc-catalysed reaction of 3-nitro-2-phenyl-2<i>H</i>-chromenes with stabilized azomethine ylides generated from the imines based on methyl glycinate and arylaldehydes leads to a mixture of <i>endo</i> and <i>endo</i>’ isomers of the corresponding chromeno[3,...

Full description

Bibliographic Details
Main Authors: Ivan A. Kochnev, Alexey Y. Barkov, Nikita S. Simonov, Maria V. Ulitko, Nikolay S. Zimnitskiy, Vladislav Y. Korotaev, Vyacheslav Y. Sosnovskikh
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Molecules
Subjects:
3-nitro-2<i>H</i>-chromenes
azomethine ylides
Michael addition/Mannich reaction sequence
chromeno[3,4-<i>c</i>]pyrrolidines
cytotoxicity
Online Access:https://www.mdpi.com/1420-3049/27/24/8983

Internet

https://www.mdpi.com/1420-3049/27/24/8983

Similar Items