Tetrahedron

[1, 2]-Wittig rearrangement from chloromethyl ethers

C Gómez, B Maciá, VJ Lillo, M Yus

Index: Gomez, Cecilia; Macia, Beatriz; Lillo, Victor J.; Yus, Miguel Tetrahedron, 2006 , vol. 62, # 42 p. 9832 - 9839

Full Text: HTML

Citation Number: 16

Abstract

The reaction of different chloromethyl ethers 1 with an excess of lithium powder and a catalytic amount of 4, 4′-di-tert-butylbiphenyl (2.5 mol%) in THF at 0° C leads to the corresponding α-lithiomethyl ether intermediates, through a chlorine–lithium exchange, which spontaneously undergo a clean [1, 2]-Wittig rearrangement affording the expected homobenzylic alcohols 2. This is the first version of this rearrangement starting from easily ...

Related Articles:

A new synthesis of chloromethyl benzyl ethers

[Benneche, Tore; Strande, Per; Undheim, Kjell Synthesis, 1983 , # 9 p. 762 - 763]

A new synthesis of chloromethyl benzyl ethers

[Benneche, Tore; Strande, Per; Undheim, Kjell Synthesis, 1983 , # 9 p. 762 - 763]

More Articles...