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). © 2010 The Royal Society of Chemistry and Owner Societies.
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CITATION STYLE
Bando, K., Zako, T., Sakono, M., Maeda, M., Wada, T., Nishijima, M., … Inoue, Y. (2010). Bio-supramolecular photochirogenesis with molecular chaperone: Enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylate mediated by prefoldin. Photochemical and Photobiological Sciences, 9(5), 655–660. https://doi.org/10.1039/b9pp00186g
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