Enantiomerically Pure α,β-Unsaturated Five-Membered-Ring Aldehydes by Ring Contraction of Epoxyhexopyranosides
Author:
Affiliation:
1. Organic Chemistry 2, Center for Chemistry and Chemical Engineering, Lund University, P.O. Box 124, S-221 00 Lund, Sweden
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo970666k
Reference22 articles.
1. Lithium salt catalyzed epoxide-carbonyl rearrangement. I. Alkyl-substituted epoxides
2. REARRANGEMENTS OF EPOXY ALCOHOLS AND RELATED COMPOUNDS. A REVIEW
3. New route to cyclopentene-1-carboxaldehydes by rearrangement of 2,3-epoxycyclohexanols
4. Mechanism of cyclopentene-1-carboxaldehyde formation by ring contraction of 2,3-epoxycyclohexanols. Improved synthetic procedures
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