Reductive electrophilic substitution of diarylmethyl methyl ethers: Synthetic applications

Article abstract of DOI:10.1080/00397919408012636

The reductive cleavage of diarylmethyl methyl ethers with Li metal in THF led to quantitative formation of the corresponding diarylmethyl anions. Quenching with electrophiles afforded substituted diarylmethanes in good to excellent yields.

Full text of DOI:10.1080/00397919408012636

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Synthetic Communications: An
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Organic Chemistry
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Reductive Electrophilic
Substitution of Diarylmethyl
Methyl Ethers: Synthetic
Applications
a
a
b
Ugo Azzena , Giovanni Melloni , Emma Fenude ,
b
b
b
Clara Finà , Mauro Marchetti & Barbara Sechi
a
Dipartimento di Chimica , Università di Sassari ,
via Vienna 2, I-07100, Sassari
b
Istituto A. T. C. A. P. A., C. N. R. , via Vienna 2,
I-07100, Sassari, Italy
Published online: 23 Sep 2006.
To cite this article: Ugo Azzena , Giovanni Melloni , Emma Fenude , Clara Finà ,
Mauro Marchetti & Barbara Sechi (1994) Reductive Electrophilic Substitution of
Diarylmethyl Methyl Ethers: Synthetic Applications, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 24:5,
591-599, DOI: 10.1080/00397919408012636
To link to this article: http://dx.doi.org/10.1080/00397919408012636
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