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pubmed-article:16496478pubmed:abstractTextCyclization reactions of lapachol (1) isolated from Heterophragma adenophyllum have been studied under microwave irradiation under different conditions using alumina (acidic, basic and neutral)/silica gel/montmorillonite (KSF and K-10) as solid support along with neat reaction using 2-3 drops of DMF giving naturally occurring dehydro-alpha-lapachone (2), alpha-lapachone (3), beta-lapachone (4) depending upon the nature of support and irradiation time. A novel naphthoquinone derivative adenophyllone (5) can be synthesized from lapachol using DMF under microwaves.lld:pubmed
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pubmed-article:16496478pubmed:authorpubmed-author:NataniKKlld:pubmed
pubmed-article:16496478pubmed:authorpubmed-author:DandiaAAlld:pubmed
pubmed-article:16496478pubmed:authorpubmed-author:AryaKKlld:pubmed
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pubmed-article:16496478pubmed:pagination207-12lld:pubmed
pubmed-article:16496478pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16496478pubmed:year2006lld:pubmed
pubmed-article:16496478pubmed:articleTitleMicrowave-assisted rapid cyclization of lapachol, a main constituent of Heterophragma adenophyllum.lld:pubmed
pubmed-article:16496478pubmed:affiliationDepartment of Chemistry, University of Rajasthan, Jaipur-302004, India. pahupsingh@yahoo.co.uklld:pubmed
pubmed-article:16496478pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16496478pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed