Abstract
The enantioselective total synthesis of the limonoids khayasin, proceranolide and mexicanolide was achieved via a convergent strategy utilizing a tactic aimed at incorporating natural products as advanced intermediates. This extended biomimetically inspired approach additionally achieved the enantioselective total synthesis of the intermediates azedaralide and cipadonoid B.
Original language | English |
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Pages (from-to) | 8913-8921 |
Number of pages | 9 |
Journal | The Journal of Organic Chemistry |
Volume | 77 |
Issue number | 20 |
DOIs | |
Publication status | Published - 19 Oct 2012 |
Externally published | Yes |