Abstract
The tropolone subunit of the naturally occurring alkaloid rubrolone aglycon is synthesized via a short reaction sequence starting with a 1,3-dipolar cycloaddition of a pyrylium ylide and indenone, followed by enone oxidation, oxygen bridge elimination and finally hydroxy group oxidation.
Original language | English |
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Pages (from-to) | 86-88 |
Number of pages | 3 |
Journal | Tetrahedron Letters |
Volume | 51 |
Issue number | 1 |
DOIs | |
Publication status | Published - 06 Jan 2010 |
ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery