Asymmetric Synthesis of Highly Functionalized 8-Oxabicyclo[3.2.1]octene Derivatives
Author:
Affiliation:
1. Contribution from the Department of Chemistry, State University of New York at Buffalo, Buffalo, New York 14260-3000
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja962081y
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1. A simple route to the 8-oxabicyclo[3.2.1]octyl and 9-oxabicyclo[3.3.1]nonyl systems. Synthesis of the 8-oxa analog of cocaine.
2. An Example of the influence of Stereochemistry of a Proximate Methyl Substituent on Keto-Enol Tautomerism
3. Total Synthesis of Furanether B. An Application of a [3 + 4] Annulation Strategy
4. Stereoselective Synthesis of cis-2,5-Disubstituted Tetrahydrofurans Using Oxabicyclo[3.2.1]heptanone Platforms. Building Blocks for Natural Product Synthesis
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