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Original courtesy of Wikipedia: http://en.wikipedia.org/wiki/Diastereomeric_excess — Please support Wikipedia.
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2 news items

 
Medgadget.com (blog)
Wed, 06 Jan 2016 22:03:20 -0800

This report on Chiral Chemicals focuses on the different methods and applications of Chiral Chemicals and their impact. Various Chiral Chemical preparation and separation methods include Traditional, Asymmetric, Biological and Other. Pharmaceuticals ...

Chemistry World

Chemistry World
Thu, 27 May 2010 00:00:00 -0700

Treating this with a strong base - in the presence of a chiral diamine to direct the deprotonation - allowed the team to form a chiral carbon-tin bond in high diastereomeric excess. In this case, the source of chirality was a '(+)-sparteine surrogate ...
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