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A chromium-free synthesis of enantiopure 5-oxoborneol

Academic Article
Publication Date:
2011
abstract:
Enantiopure (-)-5-oxoborneol was obtained in 35% overall yield in two steps, starting from readily available (-)-bornyl acetate and using oxone (R) as a safe and inexpensive oxidant. The reported procedure avoids the use of large excess of noxious chromium(VI), which was required by the so far reported syntheses.
Iris type:
01.01 Articolo in rivista
Keywords:
Borneol; Camphor; Catalysis; Oxidation; Oxone (R); Ruthenium; Terpene
List of contributors:
Tartaggia, Stefano
Authors of the University:
TARTAGGIA STEFANO
Handle:
https://iris.cnr.it/handle/20.500.14243/462711
Published in:
TETRAHEDRON LETTERS
Journal
  • Overview

Overview

URL

https://doi.org/10.1016/j.tetlet.2011.06.076
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