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A succinct access to ω-hydroxylated jasmonates via olefin metathesis.
Jimenez-Aleman, Guillermo H; Seçinti, Selina; Boland, Wilhelm.
Afiliação
  • Jimenez-Aleman GH; Department of Bioorganic Chemistry, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany.
  • Seçinti S; Department of Bioorganic Chemistry, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany.
  • Boland W; Department of Bioorganic Chemistry, Max Planck Institute for Chemical Ecology, 07745 Jena, Germany.
Z Naturforsch C J Biosci ; 72(7-8): 285-292, 2017 Jul 14.
Article em En | MEDLINE | ID: mdl-28665793
ABSTRACT
In higher plants, jasmonates are lipid-derived signaling molecules that control many physiological processes, including responses to abiotic stress, defenses against insects and pathogens, and development. Among jasmonates, ω-oxidized compounds form an important subfamily. The biological roles of these ω-modified derivatives are not fully understood, largely due to their limited availability. Herein, a brief (two-step), simple and efficient (>80% yield), versatile, gram-scalable, and environmentally friendly synthetic route to ω-oxidized jasmonates is described. The approach utilizes olefin cross-metathesis as the key step employing inexpensive, commercially available substrates and catalysts.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ciclopentanos / Alcenos / Oxilipinas / Modelos Químicos Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ciclopentanos / Alcenos / Oxilipinas / Modelos Químicos Idioma: En Ano de publicação: 2017 Tipo de documento: Article