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Aryl Methyl Ethers by Boron Tribromide

Demethylation of Aryl Methyl Ethers by Boron Tribromide [Pg.66]

Boron tribromide reacts with ethers by the sequence shown (22). The boron complex [Pg.66]

Compound Starting temp. CC) Moles BBrj compound mp of product (T) Yield (%) [Pg.67]

for example, A. I. Vogel, Practical Organic Chemistry, 3rd ed., p. 973. Longmans, London, 1956. [Pg.67]

One of the most powerful tools for the formation of cyclic molecules is the Diels-Alder reaction (/). The reaction generally involves the combination of a diene with a dienophile according to the diagram. There are surprisingly few limitations on the [Pg.71]


Xn. Demethylation of Aryl Methyl Ethers by Boron Tribromide... [Pg.66]


See other pages where Aryl Methyl Ethers by Boron Tribromide is mentioned: [Pg.151]    [Pg.611]   


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3-Aryl-5-methyl

Aryl boronate

Aryl boronates

Aryl ethers

Aryl methyl ethers

Aryl-borons

Boron aryls

Boron tribromide

Methyl tribromide

Tribromide

Tribromides

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