Functionalized Grignard reagents reactivity

In contrast to alcohols with their nch chemical reactivity ethers (compounds contain mg a C—O—C unit) undergo relatively few chemical reactions As you saw when we discussed Grignard reagents m Chapter 14 and lithium aluminum hydride reduc tions m Chapter 15 this lack of reactivity of ethers makes them valuable as solvents m a number of synthetically important transformations In the present chapter you will learn of the conditions m which an ether linkage acts as a functional group as well as the methods by which ethers are prepared... 

Method G is used to introduce the alkyl fragment when less reactive alkenes are employed or for cases where functionality within the dienophilic alkene undergoes reaction with the Grignard reagent. Following this procedure, a lithium anion is first added to the aldehyde 5 at 78 °C.27 After consumption of the aldehyde has been determined by TLC, the dienophile is added and magnesium bromide is introduced. The cycloaddition occurs as the reaction warms to room temperature. In the case of... 

Sihcon chemistry also provides a means for preparing dendrimers capped with metal ions [3,65]. For example, ferrocene [78,79], Co +, [80], Ru [81], and [9] have been hnked to the periphery of sihcon-based dendrimers. These materials are prepared by displacing reactive Si-Cl functional groups with any of a variety of nucleophiles, such as amines, alcohols, or Grignard reagents, containing the metal complexes or hgands. 

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