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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/16441
Title: Utility of polymer-supported reagents in the total synthesis of lamellarins
Authors: Poonsakdi Ploypradith
Rachel Kirk Kagan
Somsak Ruchirawat
Chulabhorn Research Institute
California State University Chico
The Institute of Science and Technology for Research and Development, Mahidol University
Keywords: Chemistry
Issue Date: 24-Jun-2005
Citation: Journal of Organic Chemistry. Vol.70, No.13 (2005), 5119-5125
Abstract: Four solid-supported reagents have been utilized in the multistep synthesis of lamellarins. The use of Amberlyst A-26 Br3- and polymer bound pyridine hydrobromide perbromide (PVPHP) for keto α-bromination of the less studied ortho-substituted acetophenone derivatives selectively furnished the corresponding monobromination products (phenacyl bromide derivatives), which were used directly in condensation reactions with benzyldihydroisoquinoline mediated by Amberlyst A-26 NaCO 3-. The 2H-pyrrole carbonates subsequently underwent intramolecular Friedel-Crafts transacylation followed by lactonization to provide the lamellarin skeleton. Alternatively, Amberlyst A-26 NaCO 3- effectively served as base in condensation reaction of benzyldihydroisoquinoline with α-nitrocinnamate derivatives to provide the corresponding 2-ethoxycarbonyl pyrroles, which smoothly underwent O-debenzylation reaction followed by lactonization to furnish the lamellarin skeleton. The novel Amberlyst-15 mediated lactonization reactions effectively combined the otherwise two separate steps into a single transformation. © 2005 American Chemical Society.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=20844458108&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/16441
ISSN: 00223263
Appears in Collections:Scopus 2001-2005

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