Tritylation of alcohols under mild conditions without using silver salts
Document Type
Article
Publication Date
1-1-2016
Abstract
© 2016 Elsevier Ltd Secondary alcohols were conveniently tritylated under mild conditions within a short running time with tritylium trifluoroacetate generated in situ from trityl alcohols and trifluoroacetic anhydride. No expensive silver salts were needed for the reactions. Four secondary alcohols were tritylated with both mono- and dimethoxy trityl alcohols giving good to excellent isolated yields. The reaction was also tested on four nucleoside derivatives that have primary alcohols. Satisfactory results were also obtained.
Publication Title
Tetrahedron Letters
Recommended Citation
Shahsavari, S.,
Chen, J.,
Wigstrom, T.,
Gooding, J.,
Gauronskas, A.,
&
Fang, S.
(2016).
Tritylation of alcohols under mild conditions without using silver salts.
Tetrahedron Letters,
57(34), 3877-3880.
http://doi.org/10.1016/j.tetlet.2016.07.062
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/7156