Dyotropic rearrangements in natural product total synthesis and biosynthesis
Author:
Affiliation:
1. Department of Chemistry
2. University of California
3. Berkeley
4. USA
5. Department of Chemistry and Pharmacy
6. Ludwig-Maximilians-Univeristy Munich
7. 81377 Munich
8. Germany
Abstract
Some recent examples of dyotropic rearrangements involved in complex natural product total synthesis and biosynthesis are highlighted.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/NP/C7NP00005G
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5. The Stabilization of Bridged Structures of Ethanes
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