Literature DB >> 14502700

Highly functionalized organomagnesium reagents prepared through halogen-metal exchange.

Paul Knochel1, Wolfgang Dohle, Nina Gommermann, Florian F Kneisel, Felix Kopp, Tobias Korn, Ioannis Sapountzis, Viet Anh Vu.   

Abstract

Organomagnesium reagents occupy a central position in synthetic organic and organometallic chemistry. Recently, the halogen-magnesium exchange has considerably extended the range of functionalized Grignard reagents available for synthetic purposes. Functional groups such as esters, nitriles, iodides, imines, or even nitro groups can be present in a wide range of aromatic and heterocyclic organomagnesium reagents. Also various highly functionalized alkenyl magnesium species can be prepared. These recent developments as well as new applications of organomagnesium reagents in cross-coupling reactions and amination reactions will be covered in this Review.

Entities:  

Year:  2003        PMID: 14502700     DOI: 10.1002/anie.200300579

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  58 in total

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8.  Nickel/bis(oxazoline)-catalyzed asymmetric Kumada reactions of alkyl electrophiles: cross-couplings of racemic alpha-bromoketones.

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9.  Synthesis of the spiroiminal moiety and approaches to the synthesis of marineosins A and B.

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10.  Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions.

Authors:  John D Nguyen; Erica M D'Amato; Jagan M R Narayanam; Corey R J Stephenson
Journal:  Nat Chem       Date:  2012-10       Impact factor: 24.427

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