Intramolecular hydroamination reactions catalyzed by zirconium complexes bearing bridged bis(phenolato) ligands
Author:
Affiliation:
1. Key Laboratory of Organic Synthesis of Jiangsu Province
2. College of Chemistry
3. Chemical Engineering and Materials Science
4. Dushu Lake Campus
5. Soochow University
Abstract
Cationic species derived from zirconium complexes stabilized by bridged bis(phenolato) ligands showed good activities in catalyzing intramolecular hydroamination/cyclization of primary and secondary amines.
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/RA/C5RA23270H
Reference62 articles.
1. Early Transition Metal (Group 3–5, Lanthanides and Actinides) and Main Group Metal (Group 1, 2, and 13) Catalyzed Hydroamination
2. Late Transition Metal-Catalyzed Hydroamination
3. Asymmetric Hydroamination
4. Late Transition Metal-Catalyzed Hydroamination and Hydroamidation
5. Recent advances in metal free- and late transition metal-catalysed hydroamination of unactivated alkenes
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