The total synthesis of alternaric acid and progress toward the synthesis of subglutinol Public Deposited

Analytics

Downloadable Content

Download PDF
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
DOI
Resource type
Rights statement
  • In Copyright
Advisor
  • Johnson, Jeffrey
Language
Access
  • Open access
Parents:

This work has no parents.

Items

Thumbnail Title Date Uploaded Visibility Actions
Fx719n47j?file=thumbnail The total synthesis of alternaric acid and progress toward the synthesis of subglutinol 2019-04-11 Public