Recent advances in the semi-pinacol rearrangement of α-hydroxy epoxides and related compounds
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2007/CS/B709634H
Reference72 articles.
1. Stereoselective construction of quaternary centers at ambient temperature by the highly stereocontrolled migration of groups containing sp-, sp2-, and sp3-hybridized carbon atoms
2. Stereoselective rearrangements of conformationally mobile epoxides
3. New route to cyclopentene-1-carboxaldehydes by rearrangement of 2,3-epoxycyclohexanols
4. Asymmetric pinacol-type rearrangement of α-hydroxy methanesulfonates promoted by triethylaluminum — preparation of optically pure α-aryl and α-vinyl ketones —
5. Catalytic version of epoxy silyl ether rearrangements
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