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The Total Synthesis of Retrojusticidin B, Justicidin E, and Helioxanthin.
- Source :
-
Journal of Organic Chemistry . 7/3/2015, Vol. 80 Issue 13, p6708-6714. 7p. - Publication Year :
- 2015
-
Abstract
- Making use of a tandem free radical cyclization process mediated by Mn(OAc)3 as a key operation, the total synthesis of retrojusticidin B, justicidin E, and helioxanthin has been concisely achieved in four or five steps in an overall yield of 45, 33 and 44%, respectively, from a common starting material 5. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00223263
- Volume :
- 80
- Issue :
- 13
- Database :
- Academic Search Index
- Journal :
- Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 108502913
- Full Text :
- https://doi.org/10.1021/acs.joc.5b00866