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Chemoinformatic Exploration of "Bioinspired Metabolomes" Illuminates Diacetyl Assembly Pathways Toward Nesteretal A-Like Cage Molecules.
Leblond, Axel; Houari, Inès; Beauxis, Yann; Leblanc, Karine; Poupon, Erwan; Beniddir, Mehdi A.
Afiliação
  • Leblond A; Équipe "Chimie des Substances Naturelles" Université Paris-Saclay, CNRS, BioCIS, 5 rue J.-B. Clément, 92290 Châtenay-Malabry, France.
  • Houari I; Équipe "Chimie des Substances Naturelles" Université Paris-Saclay, CNRS, BioCIS, 5 rue J.-B. Clément, 92290 Châtenay-Malabry, France.
  • Beauxis Y; Université de Paris, CNRS, CiTCoM, F-75006 Paris, France.
  • Leblanc K; Équipe "Chimie des Substances Naturelles" Université Paris-Saclay, CNRS, BioCIS, 5 rue J.-B. Clément, 92290 Châtenay-Malabry, France.
  • Poupon E; Équipe "Chimie des Substances Naturelles" Université Paris-Saclay, CNRS, BioCIS, 5 rue J.-B. Clément, 92290 Châtenay-Malabry, France.
  • Beniddir MA; Équipe "Chimie des Substances Naturelles" Université Paris-Saclay, CNRS, BioCIS, 5 rue J.-B. Clément, 92290 Châtenay-Malabry, France.
Org Lett ; 24(5): 1247-1252, 2022 02 11.
Article em En | MEDLINE | ID: mdl-35112872
ABSTRACT
An appealing and challenging cage structure along with an unusual biosynthetic pathway prompted us to explore an expeditious bioinspired one-pot total synthesis of nesteretal A. An unconventional strategy was chosen, and a cascade reaction starting from diacetyl was studied. Under organocatalytic conditions mimicking an aldolase, nesteretal A and a related cage analogue were anticipated by in silico metabolization, detected, targeted, and characterized.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diacetil / Frutose-Bifosfato Aldolase / Quimioinformática Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diacetil / Frutose-Bifosfato Aldolase / Quimioinformática Idioma: En Ano de publicação: 2022 Tipo de documento: Article