| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274923 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
A simple protocol for the diastereoselective synthesis of 3-nitrotetrahydroquinolines has been developed using an intramolecular nitro-Mannich reaction. In situ formation of an imine generated from treatment of 2-(2-nitroethyl)phenylamine with an aldehyde, in EtOH at room temperature, and subsequent addition of NH4OH, led to the formation of trans-products in high yield and diastereoselectivity for 15 representative examples.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
James C. Anderson, Adam Noble, Pascual Ribelles Torres,