Department of Chemistry and Center for Chemical Methodologies and Library Development, 219 Parkman Avenue, 15260 Pittsburgh, PA, USA.
Org Biomol Chem. 2012 Aug 14;10(30):5811-4. doi: 10.1039/c2ob25353d. Epub 2012 Apr 4.
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.
分子内 Staudinger-aza-Wittig 反应被用于 1,2,5,6-四氢-1,2,4-三嗪的通用合成,这是一种报道于天然产物诺拉醌的结构基序。诺拉醌的 DEF 部分通过 13 步反应以 2%的总收率得到,合成产物的结构通过 X 射线分析得到确认。