The total synthesis of alternaric acid and progress toward the synthesis of subglutinol Public Deposited
- Last Modified
- March 22, 2019
- Creator
-
Cuellar, Rebecca A. D.
- Affiliation: College of Arts and Sciences, Department of Chemistry
- Abstract
- The Oshima-Utimoto reaction coupling an allylic alcohol and butyl vinyl ether is utilized to construct the furan ring of the natural product subglutinol B. Methodology for the diastereoselective substitution of furans is also reported. Methodology utilizing silylglyoxylates as latent acyl anions for use in stereoselective multicomponent reactions is developed in the form of addition of carbon nucleophiles followed by an intermolecular aldol reaction. This methodology was then applied towards the total synthesis of alternaric acid.
- Date of publication
- May 2008
- DOI
- Resource type
- Rights statement
- In Copyright
- Advisor
- Johnson, Jeffrey
- Language
- Access
- Open access
- Parents:
This work has no parents.
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The total synthesis of alternaric acid and progress toward the synthesis of subglutinol | 2019-04-11 | Public |
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