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Trimethyl borate, reaction with Grignard reagents

Trimethyl borate, reaction with Grignard reagents, 49, 91... [Pg.80]

The synthesis of alkyl-, aryl-, and 1-alkenylboronic acids or their esters from Grignard or lithium reagents and trialkylborates is a classical and efficient method for making relatively simple boron compounds in large quantities (Scheme 2-6) [25]. The stereocontrolled synthesis of alkenylboronic acids and esters involves the reaction of a (Z)- or ( )-2-buten-2-ylmagnesium bromide with trimethyl borate [26]. [Pg.38]


See other pages where Trimethyl borate, reaction with Grignard reagents is mentioned: [Pg.795]    [Pg.611]    [Pg.294]    [Pg.870]    [Pg.346]    [Pg.354]    [Pg.356]    [Pg.494]    [Pg.96]    [Pg.96]    [Pg.184]    [Pg.184]    [Pg.197]    [Pg.117]    [Pg.170]    [Pg.184]    [Pg.184]    [Pg.197]    [Pg.96]   
See also in sourсe #XX -- [ Pg.49 , Pg.91 ]




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Boration reactions

Grignard reagents reactions

Reaction with Grignard reagents

Reactions Borates

Trimethyl borate

Trimethyl borate, reaction with

With Grignard Reagents

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