Abstract
The intramolecular [2 + 2]-photocycloaddition of the 1,3-divinyl-2- cyclopentyl tetronates 1 was performed under various conditions to give perfect diastereoselectivity and a regioselectivity of up to 85/15 in the presence of γ-cyclodextrin by differentiating the two chemically very similar double bonds of 1.
| Original language | English |
|---|---|
| Pages (from-to) | 822-824 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 2007 Jan 1 |
| Externally published | Yes |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Chemistry(all)
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry
Fingerprint Dive into the research topics of 'Regioselective [2 + 2]-photocycloaddition reactions of chiral tetronates - Influence of temperature, pressure, and reaction medium'. Together they form a unique fingerprint.
Cite this
Fleck, M., Yang, C., Wada, T., Inoue, Y., & Bach, T. (2007). Regioselective [2 + 2]-photocycloaddition reactions of chiral tetronates - Influence of temperature, pressure, and reaction medium. Chemical Communications, (8), 822-824. https://doi.org/10.1039/b613985j