Scientific article
English

Diversity-Oriented Synthesis of Diverse Polycyclic Scaffolds Inspired by the Logic of Sesquiterpene Lactones Biosynthesis

Published inAngewandte Chemie, vol. 51, no. 22, p. 5391-5394
Publication date2012
Abstract

Natural selection: An acyclic chain containing an ene-yne-ene motif, in analogy to farnesyl diphosphate, was cyclized to obtain six distinct scaffolds using different transition-metal catalysts (see scheme). Notably, the guaianolide framework was accessed through enynene metathesis enabling the synthesis of three natural products.

Keywords
  • cyclization
  • diversity-oriented synthesis
  • metathesis
  • natural products
  • transition metals
Affiliation entities Not a UNIGE publication
Citation (ISO format)
VALOT, Gaëlle et al. Diversity-Oriented Synthesis of Diverse Polycyclic Scaffolds Inspired by the Logic of Sesquiterpene Lactones Biosynthesis. In: Angewandte Chemie, 2012, vol. 51, n° 22, p. 5391–5394. doi: 10.1002/anie.201201157
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Article (Published version)
accessLevelRestricted
Identifiers
Journal ISSN1433-7851
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Technical informations

Creation12/12/2012 10:40:00
First validation12/12/2012 10:40:00
Update time14/03/2023 17:47:32
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