Repository logo

Infoscience

  • English
  • French
Log In
Logo EPFL, École polytechnique fédérale de Lausanne

Infoscience

  • English
  • French
Log In
  1. Home
  2. Academic and Research Output
  3. Journal articles
  4. Sulfur dioxide-mediated syntheses of polyfunctional alkenes and (E,Z)- and (E,E)-2,4-dien-1-ones
 
research article

Sulfur dioxide-mediated syntheses of polyfunctional alkenes and (E,Z)- and (E,E)-2,4-dien-1-ones

Bouchez, L. C.  
•
Craita, C.  
•
Vogel, P.  
2005
Organic Letters

Efficient methods for the stereoselective synthesis of polyfunctional (E)- and (2)-alkenes and conjugated (EE)- and (E,2)-dienones are presented. They rely upon one-pot, four-component processes that condense 1-oxy-1,3-dienes, silyl enol ethers, SO2, and carbon electrophiles.

  • Details
  • Metrics
Type
research article
DOI
10.1021/ol050006z
Web of Science ID

WOS:000227313400038

Author(s)
Bouchez, L. C.  
Craita, C.  
Vogel, P.  
Date Issued

2005

Published in
Organic Letters
Volume

7

Issue

5

Start page

897

End page

900

Subjects

Bond-forming reaction

•

stereoselective-synthesis

•

4-component

•

synthesis

•

methyl sulfones

•

carbonyl-compounds

•

one-pot

Note

Ecole Polytech Fed Lausanne, LGSA, CH-1015 Lausanne, Switzerland.

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219842
Logo EPFL, École polytechnique fédérale de Lausanne
  • Contact
  • infoscience@epfl.ch

  • Follow us on Facebook
  • Follow us on Instagram
  • Follow us on LinkedIn
  • Follow us on X
  • Follow us on Youtube
AccessibilityLegal noticePrivacy policyCookie settingsEnd User AgreementGet helpFeedback

Infoscience is a service managed and provided by the Library and IT Services of EPFL. © EPFL, tous droits réservés