Reductive metalation of 3,4,5-trimethoxybenzaldehyde dimethyl acetal followed by reaction with suitable electrophiles is the key step of a reaction sequence leading to the synthesis of naturally occurring 4-alkyl-3,5-dihydroxy-substituted trans-stilbenes having antibiotic activity.

Synthesis of Antibiotic Stilbenes by Reductive Metalation of 3,4,5-Trimethoxybenzaldehyde Dimethyl Acetal", Synthetic Communications, 33, 1309-1317 (2003) / Azzena, Ugo Gavino; MARIA VITTORIA, Idini; Luciano, Pilo. - In: SYNTHETIC COMMUNICATIONS. - ISSN 0039-7911. - 33:(2003), pp. 1309-1317. [10.1081/SCC-120018690]

Synthesis of Antibiotic Stilbenes by Reductive Metalation of 3,4,5-Trimethoxybenzaldehyde Dimethyl Acetal", Synthetic Communications, 33, 1309-1317 (2003)

AZZENA, Ugo Gavino;
2003-01-01

Abstract

Reductive metalation of 3,4,5-trimethoxybenzaldehyde dimethyl acetal followed by reaction with suitable electrophiles is the key step of a reaction sequence leading to the synthesis of naturally occurring 4-alkyl-3,5-dihydroxy-substituted trans-stilbenes having antibiotic activity.
2003
Synthesis of Antibiotic Stilbenes by Reductive Metalation of 3,4,5-Trimethoxybenzaldehyde Dimethyl Acetal", Synthetic Communications, 33, 1309-1317 (2003) / Azzena, Ugo Gavino; MARIA VITTORIA, Idini; Luciano, Pilo. - In: SYNTHETIC COMMUNICATIONS. - ISSN 0039-7911. - 33:(2003), pp. 1309-1317. [10.1081/SCC-120018690]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/87266
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