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

Single and Double Reductive Cleavage of C-O Bonds of Aromatic Acetals and Ketals: Generation of Benzylic Mono- and Dicarbanions / Azzena, U.G., G., M., Pisano, L., B., S.. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 35:36(1994), pp. 6759-6762. [10.1016/S0040-4039(00)73488-5]

Single and Double Reductive Cleavage of C-O Bonds of Aromatic Acetals and Ketals: Generation of Benzylic Mono- and Dicarbanions

AZZENA, Ugo Gavino;PISANO, Luisa;
1994-01-01

Abstract

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
1994
Inglese
35
36
6759
6762
4
Esperti anonimi
aromatic acetals; reductive metalation; organolithium compounds
Azzena, Ugo Gavino; G., Melloni; Pisano, Luisa; B., Sechi
Single and Double Reductive Cleavage of C-O Bonds of Aromatic Acetals and Ketals: Generation of Benzylic Mono- and Dicarbanions / Azzena, U.G., G., M., Pisano, L., B., S.. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 35:36(1994), pp. 6759-6762. [10.1016/S0040-4039(00)73488-5]
info:eu-repo/semantics/article
1 Contributo su Rivista::1.1 Articolo in rivista
262
4
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/48561
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