Design and synthesis of 3, 5- hetero diesters of 4-deoxy quinic acid and their aphicidal activity against Acyrthosiphon pisum - Laboratoire BF2i Accéder directement au contenu
Article Dans Une Revue Tetrahedron Année : 2021

Design and synthesis of 3, 5- hetero diesters of 4-deoxy quinic acid and their aphicidal activity against Acyrthosiphon pisum

Résumé

our analogs of 3,5-dicaffeoylquinic acid, including a new heterodiester of 4-deoxyquinic acid, were found toxic against the pea aphid. Several 4-deoxy quinic analogs featuring two different hydroxyl cinnamoyl moieties in position 3 and 5 were prepared for the first time and carefully analysed. Through an assay on pea aphid nymphs, interesting indications on the structure-aphicidal activity relationships and higher levels of toxicity were observed for four compounds related to the reference natural compound.
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Dates et versions

hal-03126097 , version 1 (01-06-2021)

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Paternité - Pas de modifications

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Xiubin Li, Catherine Sivignon, Pedro da Silva, Yvan Rahbé, Yves Queneau, et al.. Design and synthesis of 3, 5- hetero diesters of 4-deoxy quinic acid and their aphicidal activity against Acyrthosiphon pisum. Tetrahedron, 2021, pp.131982. ⟨10.1016/j.tet.2021.131982⟩. ⟨hal-03126097⟩
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