A practical and convenient synthesis of the fungicidal natural compound farinomalein is described starting from readily available ethyl 3-methyl-2-oxobutyrate and triethyl phosphonoacetate, employing a HornerWadsworthEmmons condensation as the key step. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.

Improved synthesis of farinomalein and its analogs / S.T. Aiwale, P. Sardi, S. Dallavalle. - In: SYNTHETIC COMMUNICATIONS. - ISSN 0039-7911. - 43:10(2013), pp. 1455-1459. [10.1080/00397911.2011.640969]

Improved synthesis of farinomalein and its analogs

S.T. Aiwale
Primo
;
P. Sardi
Secondo
;
S. Dallavalle
Ultimo
2013

Abstract

A practical and convenient synthesis of the fungicidal natural compound farinomalein is described starting from readily available ethyl 3-methyl-2-oxobutyrate and triethyl phosphonoacetate, employing a HornerWadsworthEmmons condensation as the key step. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.
Antifungal; farinomalein analogs; natural compound; synthesis
Settore CHIM/06 - Chimica Organica
Settore AGR/12 - Patologia Vegetale
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/224119
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