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Department of Chemistry and Center for Chemical Methodologies and Library Development, 219 Parkman Avenue, 15260 Pittsburgh, USA
E-mail: pwipf@pitt.edu
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Org. Biomol. Chem., 2012,10, 5811-5814
DOI:
10.1039/C2OB25353D
Received
20 Feb 2012,
Accepted
19 Mar 2012
First published online
20 Mar 2012
The intramolecular Staudinger-aza-Wittig reaction is used for a general synthesis of 1,2,5,6-tetrahydro-1,2,4-triazines, a structural motif reported for the natural product noelaquinone. The DEF moiety of noelaquinone was obtained in 13 steps and 2% overall yield, and the structure of the synthetic product was confirmed by X-ray analysis.
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Organic & Biomolecular Chemistry
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