Serendipitous synthesis of 2-alkenyl- and 2-aryl-4-thiazolidinones using dithiodiglycolic anhydride

Document Type

Article

Department or Administrative Unit

Chemistry

Publication Date

9-20-2022

Abstract

Cyclic anhydrides, including sulfur-embedded anhydrides such as thiodiglycolic anhydride, are useful dipolar synthons for the synthesis of complex organic molecules through formal cycloaddition reactions with imines (i.e., the Castagnoli–Cushman Reaction (CCR)). Here, we disclose that a disulfide-embedded anhydride (i.e., dithiodiglycolic anhydride) unexpectedly underwent an efficient formal cycloaddition with aryl aldimines to afford functionalized 4-thiazolidinones, without complications arising from the CCR. Importantly, when 1,3-azadienes were employed, the 2-alkenyl-4-thiazolidinones were obtained without complications stemming from the sulfa-Michael reaction or the Tamura reaction. These 4-thiazolidinones constitute the core of several pharmaceuticals that display a broad spectrum of biological activities, including anti-HIV and anticancer. The current tactic obviates the need for thioglycolic acid, an alternative annulation partner associated with a strongly unpleasant odor. The ensuing N,S-heterocycles are then engaged in several selective fragment growth processes, including oxidation to sulfoxides, sulfones, and epoxysulfones.

Comments

This article was originally published in New Journal of Chemistry. The full-text article from the publisher can be found here.

Due to copyright restrictions, this article is not available for free download from ScholarWorks @ CWU.

Journal

New Journal of Chemistry

Rights

© Royal Society of Chemistry 2022

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