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Please use this identifier to cite or link to this item: http://dspace.library.iitb.ac.in/jspui/handle/10054/11231

Title: Regioselective total synthesis of (+/-)neorautane, (+/-)neorautanin and their analogs. Microwave mediated synthesis of 2H-chromenes from propargyl phenyl ethers.
Authors: SUBBURAJ, K
KATOCH, R
MURUGESH, MG
TRIVEDI, GK
Keywords: 3+2 cycloaddition reactions
diels-alder reactions
substituted pterocarpans
2-alkoxy-1,4-benzoquinones
1,4-benzoquinones
products
Issue Date: 1997
Publisher: PERGAMON-ELSEVIER SCIENCE LTD
Citation: TETRAHEDRON, 53(37), 12621-12628
Abstract: Herein we describe the total synthesis of (+/-) Neorautane 1. (+/-) Neorautanin 2 and their analogs 15-18. The key intermediates Chromenes 10-13 were synthesised by microwave irradiation of propargyl phenyl ethers 8 and 9 in DMF under pressure. (C) 1997 .
URI: http://dx.doi.org/10.1016/S0040-4020(97)00783-7
http://dspace.library.iitb.ac.in/xmlui/handle/10054/11231
http://hdl.handle.net/10054/11231
ISSN: 0040-4020
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