Synthesis and Biological Activity of 2-(2-Amino-2-phenylethyl)-5-oxotetrahydrofuran-2-carboxylic Acid: A Microwave-Assisted 1,3-Dipolar Cycloaddition Approach

Author:

Denton Richard W.1ORCID,Urquilla Andromeda2,Merrer Dina C.2,Sumner Ryan1

Affiliation:

1. Department of Chemistry and Environmental Science, Medgar Evers College-CUNY

2. Department of Chemistry, Barnard College - Columbia University

Abstract

AbstractThe microwave-assisted 1,3-dipolar cycloaddition of furanyl and benzyl oximes and several methyl acrylates effectively provided several isoxazoline when mediated by diacetoxyiodobenzene. The selected isoxazoline, methyl-5-(3-methoxy-3-oxopropyl)-3-phenyl-4,5-dihydro isoxazole-5-carboxylate, was rapidly transformed to the γ-lactone carboxylic acid, 2-(2-amino-2-phenylethyl)-5-oxotetrahydrofuran-2-carboxylic acid, in reasonable yield. The biological activity of this γ-lactone carboxylic acid increased the growth of E. coli organisms by about 44% and has a potential significance in stem cell research.

Funder

National Science Foundation

Barnard College

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

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