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Total synthesis of 6′-hydroxyjusticidin A.
- Source :
- Journal of Asian Natural Products Research; Apr2012, Vol. 14 Issue 4, p322-326, 5p, 2 Diagrams, 1 Chart
- Publication Year :
- 2012
-
Abstract
- The first total synthesis of 6′-hydroxyjusticidin A, isolated from Justicia procumbens L. with good inhibitory activity against cancer cells, has been accomplished. The structure was confirmed by <superscript>1</superscript>H NMR, <superscript>13</superscript>C NMR, and HR-ESI-MS. The key steps involved a Diels–Alder cycloaddition reaction and a reduction in NaBH<subscript>4</subscript>. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10286020
- Volume :
- 14
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- Journal of Asian Natural Products Research
- Publication Type :
- Academic Journal
- Accession number :
- 78222914
- Full Text :
- https://doi.org/10.1080/10286020.2011.653561