Skip to main content

Synthesis and Reactivity of α-Halogenated, C-Protected β-Enamino Acids

Buy Article:

$55.00 plus tax (Refund Policy)

C-Protected β-enamino acids (I) reacted with one equivalent of Nhalosuccinimides (NXS) to furnish their α-halogenated derivatives (II). These compounds were then successfully transformed into halogenated uracil derivatives (III) through reaction with triphosgene, followed by 5-membered ring-opening under acidic conditions.
No References
No Citations
No Supplementary Data
No Article Media
No Metrics

Keywords: enamino acid; halogenation; oxazoline; uracil

Document Type: Review Article

Affiliations: Departamento de Quimica Organica, Universidad de Valencia, E-46100 Burjassot, Spain.

Publication date: 2004-04-01

More about this publication?
  • Letters in Organic Chemistry publishes original letters on all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is placed on publishing quality papers very rapidly. Letters are processed rapidly and take full advantage of the Internet technology both for the submission and the review of the manuscripts.
    The journal is essential reading for all organic chemists both in academia and industry.
  • 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
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