Diastereoselective Rh-Mediated Construction of 2,3,5-Trisubstituted Tetrahydrofurans
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo960758u
Reference29 articles.
1. 2,3,5-trisubstituted tetrahydrofurans by Rh-mediated cyclization of an α-diazo ester
2. Tandem Aldol-Cyclization Sequence for the Construction of Cyclic Ethers. The Formation of Substituted Tetrahydrofurans
3. Stereocontrolled preparation of tetrahydrofurans from acid-promoted rearrangements of allylic acetals
4. Acid-promoted reaction of cyclic allylic diols with carbonyl compounds. Stereoselective ring-enlarging tetrahydrofuran annulations
5. General approach to halogenated tetrahydrofuran natural products from red algae of the genus Laurencia. Total synthesis of (.+-.)-trans-kumausyne and demonstration of an asymmetric synthesis strategy
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