Nickel-Catalyzed Coupling of Aryl O-Carbamates With Grignard Reagents: 2,7-Dimethylnaphthalene-Reference-Cited by-同舟云学术

Nickel-Catalyzed Coupling of Aryl O-Carbamates With Grignard Reagents: 2,7-Dimethylnaphthalene

Published:2003-04-28 Issue: Volume: Page:42-42
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Container-title:Organic Syntheses
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Author:

Dallaire Carol¹,Kolber Isabelle²,Gingras Marc³⁴

Affiliation:

1. MDS Pharma Services; Laboratoire de Synthèse; 865 Boulevard Michèle-Bohec Blainville QC Canada J7C 5J6

2. Université Libre de Bruxelles; CP 160/08 50 Ave. F. D. Roosevelt Brussels Belgium 1050

3. Université Libre de Bruxelles; Laboratory of Supramolecular Chemistry and Catalysis; Organic Chemistry Division; CP 160-06 50 Ave. F. D. Roosevelt Brussels Belgium 1050

4. University of Nice-Sophia Antipolis; Department of Chemistry; Faculty of Sciences; 28 Parc Valrose Nice Cedex 2 France 06108

Publisher

John Wiley & Sons, Inc.

Reference14 articles.

1. Kolber , I. 1997

2. Nickel(0)-catalyzed cross coupling of aryl O-carbamates and aryl triflates with Grignard reagents. Directed ortho metalation-aligned synthetic methods for polysubstituted aromatics via a 1,2-dipole equivalent

3. An Efficient Synthesis of Functionalized Helicenes

4. [2.2]Naphthalenophanes from intermolecular [2 + 2] photocycloadditions of divinylnaphthalenes

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