Elender, Kurt and Noeth, Heinrich and Riebel, Peter and Weber, Andreas and Sauer, Jürgen (2000) 1,3-dipolar cycloaddition reactions of stable bicyclic and monocyclic azomethine ylides: Preparative aspects. TETRAHEDRON, 56 (30). pp. 5443-5463. ISSN 0040-4020
Full text not available from this repository. (Request a copy)Abstract
Stable bicyclic, monocyclic and aromatic azomethine ylides 1, 13 and 16 add angle-strained, electron-rich and electron-poor alkynes as well as alkenes and heterocumulenes to form 1:1-adducts in highly stereoselective 1,3-dipolar cycloadditions. Unsymmetrical dipalarophiles react in a regiospecific manner. (C) 2000 Elsevier Science Ltd. All rights reserved.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | 3,4-DIAZANORCARADIENES; PRECURSORS; azomethine ylides; 1,3-dipolar cycloadditions; alkynes; alkenes; regiochemistry |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Organische Chemie |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 30 Mar 2022 12:24 |
| Last Modified: | 30 Mar 2022 12:24 |
| URI: | https://pred.uni-regensburg.de/id/eprint/42314 |
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