Talk:Sharpless epoxidation
From Wikipedia, the free encyclopedia
 |
This article is within the scope of WikiProject Chemistry, which collaborates on Chemistry and related subjects on Wikipedia. To participate, help improve this article or visit the project page for details on the project. | ||
|
Article Grading: The article has not been rated for quality and/or importance yet. Please rate the article and then leave comments here to explain the ratings and/or to identify the strengths and weaknesses of the article.. |
|||
It's unclear to me what determines the entatioselectivity of the reaction. Can someone clarify that a bit? Even from his article on Organic Syntheses, I can't seem to make it out. He's producing a 2S, 3S product, but can you produce a 2R, 3R product and if so, how?
- It's the asymmetric environment of the diethyl tartrate. I'll try to build on this article soon. ~K 20:00, 26 November 2006 (UTC)
- Wow! Thanks for the nearly instantaneous response. And sorry for not signing my previous post. I suspected it was the DET but I wasn't sure. -- Pdavis68 20:02, 26 November 2006 (UTC)
