SynOpen
(Oct 2022)
A Practical and Economical Route to (S)-Glycidyl Pivalate
Jeffrey M. Noble,
Le Chang,
Dan Chen,
Binglin Wang,
Raymond N. Dominey,
Daniel W. Cook,
Justina M. Burns,
Rodger W. Stringham,
Flavio S. P. Cardoso,
David R. Snead
Affiliations
Jeffrey M. Noble
Medicines for All Institute
Le Chang
WuXi AppTec (Wuhan) Co. Ltd., Wuhan East Lake High-tech Development Zone
Dan Chen
WuXi AppTec (Wuhan) Co. Ltd., Wuhan East Lake High-tech Development Zone
Binglin Wang
WuXi AppTec (Wuhan) Co. Ltd., Wuhan East Lake High-tech Development Zone
Raymond N. Dominey
Department of Chemistry, Gottwald Center for the Sciences, University of Richmond
Daniel W. Cook
Medicines for All Institute
Justina M. Burns
Medicines for All Institute
Rodger W. Stringham
Medicines for All Institute
Flavio S. P. Cardoso
Medicines for All Institute
David R. Snead
Medicines for All Institute
DOI
https://doi.org/10.1055/s-0042-1751375
Journal volume & issue
Vol. 06,
no. 04
pp.
258
– 262
Abstract
Read online
An efficient method to prepare enantiopure (S)-glycidyl pivalate from (R)-epichlorohydrin and pivalic acid is reported. This work provides an alternative to the synthesis of this important building block from readily available and inexpensive materials.
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