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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/11791

Title: Regioselective total synthesis of edulane and its angular analogue
Authors: SUBBURAJ, K
MURUGESH, MG
TRIVEDI, GK
Keywords: 1,4-benzoquinones
pterocarpans
styrenes
Issue Date: 1997
Publisher: ROYAL SOC CHEMISTRY
Citation: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, (12), 1875-1878
Abstract: Herein we describe a 10-step total synthesis of edulane 3 and its angular analogue 18 from phloroglucinol. The key step involves ZnCl2-catalysed condensation of the appropriately substituted 2H-chromenes 8, 9 and 10 with the 2-alkoxy-1,4-benzoquinones 11 and 12, respectively.
URI: http://dx.doi.org/10.1039/a608227k
http://dspace.library.iitb.ac.in/xmlui/handle/10054/11791
http://hdl.handle.net/10054/11791
ISSN: 0300-922X
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