Abstract
Photocyclodimerization of 2-anthracenecarboxylate mediated by molecular chaperone protein was performed for the first time to afford chiral syn-head-to-tail and anti-head-to-head dimers (2 and 3) in 10% and 16% enantiomeric excess, respectively, with enhanced yields of sterically and electrostatically less-favored head-to-head dimers (3 and 4).
Original language | English |
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Pages (from-to) | 655-660 |
Number of pages | 6 |
Journal | Photochemical and Photobiological Sciences |
Volume | 9 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2010 |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry