Bio-supramolecular photochirogenesis with molecular chaperone: Enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylate mediated by prefoldin

23Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free