Skip to main content
padlock icon - secure page this page is secure

Chiral N-Acetyl Selone-Promoted Aldol Reactions

Buy Article:

$55.00 + tax (Refund Policy)

The chiral oxazolidineselone functionality was found to be an excellent partner in the stereospecific acetate aldol reaction with aldehydes via the titanium enolates. Good stereocontrol was obtained as determined by NMR spectroscopy. The oxazolidineselone also provided a straightforward way to establish the stereopurity of the coupling reaction through 77Se NMR spectroscopy.
No Reference information available - sign in for access.
No Citation information available - sign in for access.
No Supplementary Data.
No Article Media
No Metrics

Keywords: 77Se NMR spectroscopy; Acetate aldol; enolate structure; selenocarbonyl

Document Type: Research Article

Affiliations: 1: National Stable Isotope Resource, Bioenergy and Environmental Sciences Group (B8), Los Alamos National Laboratory, Los Alamos, New Mexico, USA 2: Advanced Measurement Science Group (B9), Bioscience Division, Los Alamos National Laboratory, Los Alamos, New Mexico, USA 3: NMT Division, Los Alamos National Laboratory, Bioscience Division, Los Alamos, New Mexico, USA

Publication date: 01 January 2009

  • Access Key
  • Free content
  • Partial Free content
  • New content
  • Open access content
  • Partial Open access content
  • Subscribed content
  • Partial Subscribed content
  • Free trial content
Cookie Policy
X
Cookie Policy
Ingenta Connect website makes use of cookies so as to keep track of data that you have filled in. I am Happy with this Find out more