A single-step acid catalyzed reaction for rapid assembly of NH-1, 2, 3-triazoles. Issue 59 (29th June 2016)

• Record Type: Journal Article
• Authors: Thomas, Joice; Jana, Sampad; Liekens, Sandra; Dehaen, Wim
• Is Part Of: Chemical communications. Volume 52:Issue 59(2016)
• Page Start: 9236
• Page End: 9239
• Publication Date: 2016-06-29
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c6cc03744e
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : NH -1, 2, 3-Triazole moieties are a part of the design of various biologically active compounds, pharmaceutical agents and functional materials. Abstract : NH -1, 2, 3-Triazole moieties are a part of the design of various biologically active compounds, pharmaceutical agents and functional materials. Unfortunately, the applications of this heterocycle are still underexplored due to the lack of a general synthetic protocol. Here we outline a novel, general and facile metal-free pathway that enables the direct synthesis of these heterocycles by combining readily accessible and abundant precursors such as enolizable ketones and NH4 OAc with high levels of regioselectivity via an organocascade process. The developed chemistry has been successfully applied to the synthesis of several structurally diverse products, pharmaceutical agents and supramolecular receptors.