Improved Negishi Cross-Coupling Reactions of an Organozinc Reagent Derived froml-Aspartic Acid with Monohalopyridines
Author:
Affiliation:
1. Department of Materials and Life Sciences, Faculty of Science and Technology; Sophia University; 7-1 Kioicho, Chiyoda-ku Tokyo 102-8554 Japan
Publisher
Wiley
Subject
Organic Chemistry
Reference22 articles.
1. Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides
2. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides
3. Palladium- or nickel-catalyzed cross coupling. A new selective method for carbon-carbon bond formation
4. Synthesis of enantiomerically pure protected β-aryl alanines
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