Toluates: unexpectedly versatile reagents

Lam, Kevin;Marko, Istvan
(2009) Tetrahedron — Vol. 65, n° 52, p. 10930-10940 (2009)

Files

pdfdocument.pdf
  • Restricted Access
  • Adobe PDF
  • 815.34 KB
Request a copy

Details

Authors
  • Lam, KevinUCLouvain
    Author
  • Marko, IstvanUCLouvain
    Author
Abstract
The mechanism of the monoelectronic reduction of aromatic esters has been investigated. The unexpected synthetic utility of the toluate moiety in the deoxygenation of alcohols and the allylation of ketones is also reported. Finally, the use of aromatic esters as robust, though easily removable, protecting groups is depicted. (C) 2009 Elsevier Ltd. All rights reserved.
Affiliations

Citations

  • APA
  • Chicago
  • FWB

Lam, K., & Marko, I. (2009). Toluates: unexpectedly versatile reagents. Tetrahedron, 65(52), 10930-10940. https://doi.org/10.1016/j.tet.2009.09.111 (Original work published 2009)