Abstract
The irradiation of allylically substituted dioxenone photosubstrates 6 and 21 lead to unexpected products, the formation of which can be explained by a series of transannular hydrogen atom abstractions.
Original language | English |
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Pages (from-to) | 2150-2154 |
Number of pages | 4 |
Journal | Synthesis: journal of synthetic organic chemistry |
Issue number | 14 |
DOIs | |
Publication status | Published - 2002 |
Keywords
- Cycloadditions
- Natural products
- Photochemistry
- Radicais
- Rearrangements