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Natural Product Research
Formerly Natural Product Letters
Volume 20, 2006 - Issue 2
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Original Articles

Microwave-assisted rapid cyclization of lapachol, a main constituent of Heterophragma adenophyllum

, , , &
Pages 207-212 | Received 26 Apr 2004, Accepted 17 Dec 2004, Published online: 21 Aug 2006
 

Abstract

Cyclization 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-α-lapachone (2), α-lapachone (3), β-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.

Acknowledgements

Financial assistance from UGC (New Delhi) is gratefully acknowledged. We are also thankful to RSIC, CDRI, Lucknow for recording the spectra.

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